Eleazar Eskin

Title(s)Professor, Computer Science
SchoolHenry Samueli School of Engineering and Applied Science
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    Other Positions
    Title(s)Professor, Human Genetics

    Title(s)Professor, Computational Medicine


    Collapse Research 
    Collapse Research Activities and Funding
    Computational Genomics Summer Institute and Mentoring Network
    NIH R25GM135043May 1, 2020 - Apr 30, 2025
    Role: Principal Investigator
    Undergraduate Research Experiences in Neurogenetics and Neurogenomics
    NIH R25NS115554Dec 15, 2019 - Nov 30, 2024
    Role: Principal Investigator
    Genetic pathways for impulsivity and drug reinforcement: DNA and transcriptome variation in mice
    NIH U01DA041602Sep 15, 2017 - May 31, 2022
    Role: Co-Principal Investigator
    Undergraduate Research Experience in Neuropsychiatric Genomics
    NIH R25MH109172Feb 1, 2016 - Nov 30, 2021
    Role: Co-Principal Investigator
    Mathematical and Computational Approaches in High-Throughput Genomics Training
    NIH R25GM112625Sep 1, 2015 - Jun 30, 2021
    Role: Principal Investigator
    Correcting for Population Structure in Gene-by-Environment Interaction Studies
    NIH R01ES022282Sep 1, 2013 - Jun 30, 2018
    Role: Principal Investigator
    Discovering the Genetic Basis of Hypertension
    NIH K25HL080079Jun 1, 2006 - May 31, 2012
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Packaging and containerization of computational methods. Nat Protoc. 2024 Apr 02. Alser M, Lawlor B, Abdill RJ, Waymost S, Ayyala R, Rajkumar N, LaPierre N, Brito J, Ribeiro-Dos-Santos AM, Almadhoun N, Sarwal V, Firtina C, Osinski T, Eskin E, Hu Q, Strong D, Kim BBD, Abedalthagafi MS, Mutlu O, Mangul S. PMID: 38565959.
      View in: PubMed   Mentions:    Fields:    
    2. Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer's Disease. medRxiv. 2024 Feb 06. Fu M, Tran T, Eskin E, Lajonchere C, Pasaniuc B, Geschwind DH, Vossel K, Chang TS. PMID: 38370677; PMCID: PMC10871371.
      View in: PubMed   Mentions:
    3. 3D Printing as an Effective Quality Assurance Implementation in Massive-Scale SARS-CoV-2 Testing at a SwabSeq Next-Generation Sequencing Laboratory. Lab Med. 2023 Sep 05; 54(5):512-518. Sathe LM, Khan NN, Williams JM, Saul R, Jajieh K, Sartippour MR, Young R, Xie J, Marquette DM, Duncan T, Eskin E, Arboleda VA. PMID: 36810591.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    4. Genetic pathways regulating the longitudinal acquisition of cocaine self-administration in a panel of inbred and recombinant inbred mice. Cell Rep. 2023 08 29; 42(8):112856. Khan AH, Bagley JR, LaPierre N, Gonzalez-Figueroa C, Spencer TC, Choudhury M, Xiao X, Eskin E, Jentsch JD, Smith DJ. PMID: 37481717; PMCID: PMC10530068.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    5. Leveraging family data to design Mendelian randomization that is provably robust to population stratification. Genome Res. 2023 07; 33(7):1032-1041. LaPierre N, Fu B, Turnbull S, Eskin E, Sankararaman S. PMID: 37197991; PMCID: PMC10538495.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. RNA-seq data science: From raw data to effective interpretation. Front Genet. 2023; 14:997383. Deshpande D, Chhugani K, Chang Y, Karlsberg A, Loeffler C, Zhang J, Muszynska A, Munteanu V, Yang H, Rotman J, Tao L, Balliu B, Tseng E, Eskin E, Zhao F, Mohammadi P, P Labaj P, Mangul S. PMID: 36999049; PMCID: PMC10043755.
      View in: PubMed   Mentions: 10  
    7. Leveraging family data to design Mendelian Randomization that is provably robust to population stratification. bioRxiv. 2023 Jan 06. LaPierre N, Fu B, Turnbull S, Eskin E, Sankararaman S. PMID: 36711635; PMCID: PMC9881984.
      View in: PubMed   Mentions:
    8. Accurate modeling of replication rates in genome-wide association studies by accounting for Winner's Curse and study-specific heterogeneity. G3 (Bethesda). 2022 Dec 01; 12(12). Zou J, Zhou J, Faller S, Brown RP, Sankararaman SS, Eskin E. PMID: 36250793; PMCID: PMC9713380.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    9. Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations. PLoS Genet. 2022 11; 18(11):e1010447. Taraszka K, Zaitlen N, Eskin E. PMID: 36342933; PMCID: PMC9671458.
      View in: PubMed   Mentions: 1     Fields:    
    10. Ensemble neural network model for detecting thyroid eye disease using external photographs. Br J Ophthalmol. 2023 Nov; 107(11):1722-1729. Karlin J, Gai L, LaPierre N, Danesh K, Farajzadeh J, Palileo B, Taraszka K, Zheng J, Wang W, Eskin E, Rootman D. PMID: 36126104.
      View in: PubMed   Mentions: 4     Fields:    
    11. A comprehensive benchmarking of WGS-based deletion structural variant callers. Brief Bioinform. 2022 07 18; 23(4). Sarwal V, Niehus S, Ayyala R, Kim M, Sarkar A, Chang S, Lu A, Rajkumar N, Darfci-Maher N, Littman R, Chhugani K, Soylev A, Comarova Z, Wesel E, Castellanos J, Chikka R, Distler MG, Eskin E, Flint J, Mangul S. PMID: 35753701; PMCID: PMC9294411.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansAnimals
    12. Bruins-in-Genomics: Evaluation of the impact of a UCLA undergraduate summer program in computational biology on participating students. PLoS One. 2022; 17(5):e0268861. Coller HA, Beggs S, Andrews S, Maloy J, Chiu A, Sankararaman S, Pellegrini M, Freimer N, Johnson T, Papp J, Eskin E, Hoffmann A. PMID: 35622842; PMCID: PMC9140266.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    13. Critical Assessment of Metagenome Interpretation: the second round of challenges. Nat Methods. 2022 04; 19(4):429-440. Meyer F, Fritz A, Deng ZL, Koslicki D, Lesker TR, Gurevich A, Robertson G, Alser M, Antipov D, Beghini F, Bertrand D, Brito JJ, Brown CT, Buchmann J, Buluç A, Chen B, Chikhi R, Clausen PTLC, Cristian A, Dabrowski PW, Darling AE, Egan R, Eskin E, Georganas E, Goltsman E, Gray MA, Hansen LH, Hofmeyr S, Huang P, Irber L, Jia H, Jørgensen TS, Kieser SD, Klemetsen T, Kola A, Kolmogorov M, Korobeynikov A, Kwan J, LaPierre N, Lemaitre C, Li C, Limasset A, Malcher-Miranda F, Mangul S, Marcelino VR, Marchet C, Marijon P, Meleshko D, Mende DR, Milanese A, Nagarajan N, Nissen J, Nurk S, Oliker L, Paoli L, Peterlongo P, Piro VC, Porter JS, Rasmussen S, Rees ER, Reinert K, Renard B, Robertsen EM, Rosen GL, Ruscheweyh HJ, Sarwal V, Segata N, Seiler E, Shi L, Sun F, Sunagawa S, Sørensen SJ, Thomas A, Tong C, Trajkovski M, Tremblay J, Uritskiy G, Vicedomini R, Wang Z, Wang Z, Wang Z, Warren A, Willassen NP, Yelick K, You R, Zeller G, Zhao Z, Zhu S, Zhu J, Garrido-Oter R, Gastmeier P, Hacquard S, Häußler S, Khaledi A, Maechler F, Mesny F, Radutoiu S, Schulze-Lefert P, Smit N, Strowig T, Bremges A, Sczyrba A, McHardy AC. PMID: 35396482; PMCID: PMC9007738.
      View in: PubMed   Mentions: 79     Fields:    Translation:Cells
    14. Genomic epidemiology of the Los Angeles COVID-19 outbreak and the early history of the B.1.43 strain in the USA. BMC Genomics. 2022 Apr 04; 23(1):260. Guo L, Boocock J, Hilt EE, Chandrasekaran S, Zhang Y, Munugala C, Sathe L, Alexander N, Arboleda VA, Flint J, Eskin E, Luo C, Yang S, Garner OB, Yin Y, Bloom JS, Kruglyak L. PMID: 35379194; PMCID: PMC8978495.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCellsPHPublic Health
    15. Robust Mendelian randomization in the presence of residual population stratification, batch effects and horizontal pleiotropy. Nat Commun. 2022 03 01; 13(1):1093. Cinelli C, LaPierre N, Hill BL, Sankararaman S, Eskin E. PMID: 35232963; PMCID: PMC8888767.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    16. Identifying causal variants by fine mapping across multiple studies. PLoS Genet. 2021 09; 17(9):e1009733. LaPierre N, Taraszka K, Huang H, He R, Hormozdiari F, Eskin E. PMID: 34543273; PMCID: PMC8491908.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    17. Massively scaled-up testing for SARS-CoV-2 RNA via next-generation sequencing of pooled and barcoded nasal and saliva samples. Nat Biomed Eng. 2021 07; 5(7):657-665. Bloom JS, Sathe L, Munugala C, Jones EM, Gasperini M, Lubock NB, Yarza F, Thompson EM, Kovary KM, Park J, Marquette D, Kay S, Lucas M, Love T, Sina Booeshaghi A, Brandenberg OF, Guo L, Boocock J, Hochman M, Simpkins SW, Lin I, LaPierre N, Hong D, Zhang Y, Oland G, Choe BJ, Chandrasekaran S, Hilt EE, Butte MJ, Damoiseaux R, Kravit C, Cooper AR, Yin Y, Pachter L, Garner OB, Flint J, Eskin E, Luo C, Kosuri S, Kruglyak L, Arboleda VA. PMID: 34211145; PMCID: PMC10810734.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    18. MARS: leveraging allelic heterogeneity to increase power of association testing. Genome Biol. 2021 04 30; 22(1):128. Hormozdiari F, Jung J, Eskin E, J Joo JW. PMID: 33931127; PMCID: PMC8086090.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    19. Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease. Cell. 2021 05 13; 184(10):2633-2648.e19. de Goede OM, Nachun DC, Ferraro NM, Gloudemans MJ, Rao AS, Smail C, Eulalio TY, Aguet F, Ng B, Xu J, Barbeira AN, Castel SE, Kim-Hellmuth S, Park Y, Scott AJ, Strober BJ, GTEx Consortium, Brown CD, Wen X, Hall IM, Battle A, Lappalainen T, Im HK, Ardlie KG, Mostafavi S, Quertermous T, Kirkegaard K, Montgomery SB. PMID: 33864768; PMCID: PMC8651477.
      View in: PubMed   Mentions: 56     Fields:    Translation:HumansCells
    20. Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing. medRxiv. 2021 Mar 09. Bloom JS, Sathe L, Munugala C, Jones EM, Gasperini M, Lubock NB, Yarza F, Thompson EM, Kovary KM, Park J, Marquette D, Kay S, Lucas M, Love T, Booeshaghi AS, Brandenberg OF, Guo L, Boocock J, Hochman M, Simpkins SW, Lin I, LaPierre N, Hong D, Zhang Y, Oland G, Choe BJ, Chandrasekaran S, Hilt EE, Butte MJ, Damoiseaux R, Kravit C, Cooper AR, Yin Y, Pachter L, Garner OB, Flint J, Eskin E, Luo C, Kosuri S, Kruglyak L, Arboleda VA. PMID: 32909008; PMCID: PMC7480060.
      View in: PubMed   Mentions: 2  
    21. Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors. iScience. 2021 Mar 19; 24(3):102188. Chang TS, Ding Y, Freund MK, Johnson R, Schwarz T, Yabu JM, Hazlett C, Chiang JN, Wulf DA, UCLA Precision Health Data Discovery Repository Working Group, Geschwind DH, Butte MJ, Pasaniuc B. PMID: 33615196; PMCID: PMC7879099.
      View in: PubMed   Mentions: 8  
    22. PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics. Am J Hum Genet. 2021 01 07; 108(1):36-48. Lee CH, Shi H, Pasaniuc B, Eskin E, Han B. PMID: 33352115; PMCID: PMC7820744.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    23. Genetic determinants of ammonia-induced acute lung injury in mice. Am J Physiol Lung Cell Mol Physiol. 2021 01 01; 320(1):L41-L62. Bein K, Ganguly K, Martin TM, Concel VJ, Brant KA, Di YPP, Upadhyay S, Fabisiak JP, Vuga LJ, Kaminski N, Kostem E, Eskin E, Prows DR, Jang AS, Leikauf GD. PMID: 33050709; PMCID: PMC7847062.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    24. A machine learning algorithm to increase COVID-19 inpatient diagnostic capacity. PLoS One. 2020; 15(9):e0239474. Goodman-Meza D, Rudas A, Chiang JN, Adamson PC, Ebinger J, Sun N, Botting P, Fulcher JA, Saab FG, Brook R, Eskin E, An U, Kordi M, Jew B, Balliu B, Chen Z, Hill BL, Rahmani E, Halperin E, Manuel V. PMID: 32960917; PMCID: PMC7508387.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCellsPHPublic Health
    25. The GTEx Consortium atlas of genetic regulatory effects across human tissues. Science. 2020 09 11; 369(6509):1318-1330. GTEx Consortium. PMID: 32913098; PMCID: PMC7737656.
      View in: PubMed   Mentions: 1200     Fields:    Translation:Humans
    26. Determinants of telomere length across human tissues. Science. 2020 09 11; 369(6509). Demanelis K, Jasmine F, Chen LS, Chernoff M, Tong L, Delgado D, Zhang C, Shinkle J, Sabarinathan M, Lin H, Ramirez E, Oliva M, Kim-Hellmuth S, Stranger BE, Lai TP, Aviv A, Ardlie KG, Aguet F, Ahsan H, GTEx Consortium, Doherty JA, Kibriya MG, Pierce BL. PMID: 32913074; PMCID: PMC8108546.
      View in: PubMed   Mentions: 157     Fields:    Translation:HumansCells
    27. The impact of sex on gene expression across human tissues. Science. 2020 09 11; 369(6509). Oliva M, Muñoz-Aguirre M, Kim-Hellmuth S, Wucher V, Gewirtz ADH, Cotter DJ, Parsana P, Kasela S, Balliu B, Viñuela A, Castel SE, Mohammadi P, Aguet F, Zou Y, Khramtsova EA, Skol AD, Garrido-Martín D, Reverter F, Brown A, Evans P, Gamazon ER, Payne A, Bonazzola R, Barbeira AN, Hamel AR, Martinez-Perez A, Soria JM, GTEx Consortium, Pierce BL, Stephens M, Eskin E, Dermitzakis ET, Segrè AV, Im HK, Engelhardt BE, Ardlie KG, Montgomery SB, Battle AJ, Lappalainen T, Guigó R, Stranger BE. PMID: 32913072; PMCID: PMC8136152.
      View in: PubMed   Mentions: 204     Fields:    Translation:HumansCells
    28. A vast resource of allelic expression data spanning human tissues. Genome Biol. 2020 09 11; 21(1):234. Castel SE, Aguet F, Mohammadi P, GTEx Consortium, Ardlie KG, Lappalainen T. PMID: 32912332; PMCID: PMC7488534.
      View in: PubMed   Mentions: 37     Fields:    Translation:Humans
    29. Cell type-specific genetic regulation of gene expression across human tissues. Science. 2020 09 11; 369(6509). Kim-Hellmuth S, Aguet F, Oliva M, Muñoz-Aguirre M, Kasela S, Wucher V, Castel SE, Hamel AR, Viñuela A, Roberts AL, Mangul S, Wen X, Wang G, Barbeira AN, Garrido-Martín D, Nadel BB, Zou Y, Bonazzola R, Quan J, Brown A, Martinez-Perez A, Soria JM, GTEx Consortium, Getz G, Dermitzakis ET, Small KS, Stephens M, Xi HS, Im HK, Guigó R, Segrè AV, Stranger BE, Ardlie KG, Lappalainen T. PMID: 32913075; PMCID: PMC8051643.
      View in: PubMed   Mentions: 127     Fields:    Translation:HumansCells
    30. Transcriptomic signatures across human tissues identify functional rare genetic variation. Science. 2020 09 11; 369(6509). Ferraro NM, Strober BJ, Einson J, Abell NS, Aguet F, Barbeira AN, Brandt M, Bucan M, Castel SE, Davis JR, Greenwald E, Hess GT, Hilliard AT, Kember RL, Kotis B, Park Y, Peloso G, Ramdas S, Scott AJ, Smail C, Tsang EK, Zekavat SM, Ziosi M, TOPMed Lipids Working Group, Ardlie KG, Assimes TL, Bassik MC, Brown CD, Correa A, Hall I, Im HK, Li X, Natarajan P, GTEx Consortium, Lappalainen T, Mohammadi P, Montgomery SB, Battle A. PMID: 32913073; PMCID: PMC7646251.
      View in: PubMed   Mentions: 55     Fields:    Translation:HumansCells
    31. A Quantitative Proteome Map of the Human Body. Cell. 2020 10 01; 183(1):269-283.e19. Jiang L, Wang M, Lin S, Jian R, Li X, Chan J, Dong G, Fang H, Robinson AE, GTEx Consortium, Snyder MP. PMID: 32916130; PMCID: PMC7575058.
      View in: PubMed   Mentions: 138     Fields:    Translation:HumansCells
    32. Metalign: efficient alignment-based metagenomic profiling via containment min hash. Genome Biol. 2020 09 10; 21(1):242. LaPierre N, Alser M, Eskin E, Koslicki D, Mangul S. PMID: 32912225; PMCID: PMC7488264.
      View in: PubMed   Mentions: 17     Fields:    
    33. Author Correction: Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing. Nat Commun. 2020 09 04; 11(1):4499. Mandric I, Rotman J, Yang HT, Strauli N, Montoya DJ, Van Der Wey W, Ronas JR, Statz B, Yao D, Petrova V, Zelikovsky A, Spreafico R, Shifman S, Zaitlen N, Rossetti M, Ansel KM, Eskin E, Mangul S. PMID: 32887888; PMCID: PMC7474053.
      View in: PubMed   Mentions: 1     Fields:    
    34. Correction to: Improving the usability and comprehensiveness of microbial databases. BMC Biol. 2020 07 28; 18(1):92. Loeffler C, Karlsberg A, Martin LS, Eskin E, Koslicki D, Mangul S. PMID: 32723395; PMCID: PMC7389812.
      View in: PubMed   Mentions: 1     Fields:    
    35. Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing. Nat Commun. 2020 06 19; 11(1):3126. Mandric I, Rotman J, Yang HT, Strauli N, Montoya DJ, Van Der Wey W, Ronas JR, Statz B, Yao D, Petrova V, Zelikovsky A, Spreafico R, Shifman S, Zaitlen N, Rossetti M, Ansel KM, Eskin E, Mangul S. PMID: 32561710; PMCID: PMC7305308.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansCells
    36. Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma. Nat Commun. 2020 04 15; 11(1):1776. Han Y, Jia Q, Jahani PS, Hurrell BP, Pan C, Huang P, Gukasyan J, Woodward NC, Eskin E, Gilliland FD, Akbari O, Hartiala JA, Allayee H. PMID: 32296059; PMCID: PMC7160128.
      View in: PubMed   Mentions: 66     Fields:    Translation:HumansAnimalsCells
    37. Improving the usability and comprehensiveness of microbial databases. BMC Biol. 2020 04 07; 18(1):37. Loeffler C, Karlsberg A, Martin LS, Eskin E, Koslicki D, Mangul S. PMID: 32264902; PMCID: PMC7140547.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    38. Benchmarking of computational error-correction methods for next-generation sequencing data. Genome Biol. 2020 03 17; 21(1):71. Mitchell K, Brito JJ, Mandric I, Wu Q, Knyazev S, Chang S, Martin LS, Karlsberg A, Gerasimov E, Littman R, Hill BL, Wu NC, Yang HT, Hsieh K, Chen L, Littman E, Shabani T, Enik G, Yao D, Sun R, Schroeder J, Eskin E, Zelikovsky A, Skums P, Pop M, Mangul S. PMID: 32183840; PMCID: PMC7079412.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    39. A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies. J Comput Biol. 2020 03; 27(3):418-428. Wu Y, Eskin E, Sankararaman S. PMID: 32053016; PMCID: PMC7081249.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    40. A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity. PLoS Genet. 2019 12; 15(12):e1008528. Maazi H, Hartiala JA, Suzuki Y, Crow AL, Shafiei Jahani P, Lam J, Patel N, Rigas D, Han Y, Huang P, Eskin E, Lusis AJ, Gilliland FD, Akbari O, Allayee H. PMID: 31869344; PMCID: PMC6944376.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimals
    41. Leveraging allelic imbalance to refine fine-mapping for eQTL studies. PLoS Genet. 2019 12; 15(12):e1008481. Zou J, Hormozdiari F, Jew B, Castel SE, Lappalainen T, Ernst J, Sul JH, Eskin E. PMID: 31834882; PMCID: PMC6952111.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    42. Genomic GPS: using genetic distance from individuals to public data for genomic analysis without disclosing personal genomes. Genome Biol. 2019 08 27; 20(1):175. Kim K, Baik H, Jang CS, Roh JK, Eskin E, Han B. PMID: 31455387; PMCID: PMC6712716.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    43. Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage. Nat Neurosci. 2019 09; 22(9):1521-1532. Lee C, Kang EY, Gandal MJ, Eskin E, Geschwind DH. PMID: 31455884; PMCID: PMC6750256.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    44. A linear mixed model approach to gene expression-tumor aneuploidy association studies. Sci Rep. 2019 08 16; 9(1):11944. Yao DW, Balanis NG, Eskin E, Graeber TG. PMID: 31420589; PMCID: PMC6697733.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    45. Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology. Nat Commun. 2019 07 31; 10(1):3417. Rahmani E, Schweiger R, Rhead B, Criswell LA, Barcellos LF, Eskin E, Rosset S, Sankararaman S, Halperin E. PMID: 31366909; PMCID: PMC6668473.
      View in: PubMed   Mentions: 55     Fields:    Translation:HumansCells
    46. Challenges and recommendations to improve the installability and archival stability of omics computational tools. PLoS Biol. 2019 06; 17(6):e3000333. Mangul S, Mosqueiro T, Abdill RJ, Duong D, Mitchell K, Sarwal V, Hill B, Brito J, Littman RJ, Statz B, Lam AK, Dayama G, Grieneisen L, Martin LS, Flint J, Eskin E, Blekhman R. PMID: 31220077; PMCID: PMC6605654.
      View in: PubMed   Mentions: 36     Fields:    Translation:Humans
    47. MiCoP: microbial community profiling method for detecting viral and fungal organisms in metagenomic samples. BMC Genomics. 2019 Jun 06; 20(Suppl 5):423. LaPierre N, Mangul S, Alser M, Mandric I, Wu NC, Koslicki D, Eskin E. PMID: 31167634; PMCID: PMC6551237.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimalsCells
    48. Systematic benchmarking of omics computational tools. Nat Commun. 2019 03 27; 10(1):1393. Mangul S, Martin LS, Hill BL, Lam AK, Distler MG, Zelikovsky A, Eskin E, Flint J. PMID: 30918265; PMCID: PMC6437167.
      View in: PubMed   Mentions: 57     Fields:    Translation:Humans
    49. How bioinformatics and open data can boost basic science in countries and universities with limited resources. Nat Biotechnol. 2019 03; 37(3):324-326. Mangul S, Martin LS, Langmead B, Sanchez-Galan JE, Toma I, Hormozdiari F, Pevzner P, Eskin E. PMID: 30833765.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    50. Improving the usability and archival stability of bioinformatics software. Genome Biol. 2019 02 27; 20(1):47. Mangul S, Martin LS, Eskin E, Blekhman R. PMID: 30813962; PMCID: PMC6391762.
      View in: PubMed   Mentions: 31     Fields:    
    51. Population structure in genetic studies: Confounding factors and mixed models. PLoS Genet. 2018 12; 14(12):e1007309. Sul JH, Martin LS, Eskin E. PMID: 30589851; PMCID: PMC6307707.
      View in: PubMed   Mentions: 78     Fields:    Translation:HumansAnimals
    52. Word and Sentence Embedding Tools to Measure Semantic Similarity of Gene Ontology Terms by Their Definitions. J Comput Biol. 2019 01; 26(1):38-52. Duong D, Ahmad WU, Eskin E, Chang KW, Li JJ. PMID: 30383443; PMCID: PMC6350067.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimals
    53. Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies. J Comput Biol. 2019 11; 26(11):1203-1213. Wu Y, Hormozdiari F, Joo JWJ, Eskin E. PMID: 30272994; PMCID: PMC6856942.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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    111. Accurate and fast multiple-testing correction in eQTL studies. Am J Hum Genet. 2015 Jun 04; 96(6):857-68. Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B. PMID: 26027500; PMCID: PMC4457958.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    112. Genome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss. PLoS Genet. 2015 Apr; 11(4):e1005094. Lavinsky J, Crow AL, Pan C, Wang J, Aaron KA, Ho MK, Li Q, Salehide P, Myint A, Monges-Hernadez M, Eskin E, Allayee H, Lusis AJ, Friedman RA. PMID: 25880434; PMCID: PMC4399881.
      View in: PubMed   Mentions: 39     Fields:    Translation:Animals
    113. Gene-Gene Interactions Detection Using a Two-stage Model. J Comput Biol. 2015 Jun; 22(6):563-76. Wang Z, Sul JH, Snir S, Lozano JA, Eskin E. PMID: 25871811; PMCID: PMC4449719.
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    114. Efficient multiple-trait association and estimation of genetic correlation using the matrix-variate linear mixed model. Genetics. 2015 May; 200(1):59-68. Furlotte NA, Eskin E. PMID: 25724382; PMCID: PMC4423381.
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    115. Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma. Mol Psychiatry. 2015 Dec; 20(12):1557-64. Luykx JJ, Bakker SC, Visser WF, Verhoeven-Duif N, Buizer-Voskamp JE, den Heijer JM, Boks MP, Sul JH, Eskin E, Ori AP, Cantor RM, Vorstman J, Strengman E, DeYoung J, Kappen TH, Pariama E, van Dongen EP, Borgdorff P, Bruins P, de Koning TJ, Kahn RS, Ophoff RA. PMID: 25666758.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    116. Heritability of periodontal bone loss in mice. J Periodontal Res. 2015 Dec; 50(6):730-6. Hiyari S, Atti E, Camargo PM, Eskin E, Lusis AJ, Tetradis S, Pirih FQ. PMID: 25581386; PMCID: PMC4499504.
      View in: PubMed   Mentions: 15     Fields:    Translation:AnimalsCells
    117. A spatial haplotype copying model with applications to genotype imputation. J Comput Biol. 2015 May; 22(5):451-62. Yang WY, Hormozdiari F, Eskin E, Pasaniuc B. PMID: 25526526; PMCID: PMC4425418.
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    118. Memory efficient assembly of human genome. J Bioinform Comput Biol. 2015 Apr; 13(2):1550008. Hormozdiari F, Eskin E. PMID: 25603998.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    119. IPED2X: a robust pedigree reconstruction algorithm for complicated pedigrees. J Bioinform Comput Biol. 2014 Dec; 12(6):1442007. He D, Eskin E. PMID: 25553812.
      View in: PubMed   Mentions: 2     Fields:    
    120. Spatial localization of recent ancestors for admixed individuals. G3 (Bethesda). 2014 Nov 03; 4(12):2505-18. Yang WY, Platt A, Chiang CW, Eskin E, Novembre J, Pasaniuc B. PMID: 25371484; PMCID: PMC4267945.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    121. Integrating functional data to prioritize causal variants in statistical fine-mapping studies. PLoS Genet. 2014 Oct; 10(10):e1004722. Kichaev G, Yang WY, Lindstrom S, Hormozdiari F, Eskin E, Price AL, Kraft P, Pasaniuc B. PMID: 25357204; PMCID: PMC4214605.
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    122. Identifying causal variants at loci with multiple signals of association. Genetics. 2014 Oct; 198(2):497-508. Hormozdiari F, Kostem E, Kang EY, Pasaniuc B, Eskin E. PMID: 25104515; PMCID: PMC4196608.
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    123. Privacy preserving protocol for detecting genetic relatives using rare variants. Bioinformatics. 2014 Jun 15; 30(12):i204-11. Hormozdiari F, Joo JW, Wadia A, Guan F, Ostrosky R, Sahai A, Eskin E. PMID: 24931985; PMCID: PMC4058916.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    124. Accurate viral population assembly from ultra-deep sequencing data. Bioinformatics. 2014 Jun 15; 30(12):i329-37. Mangul S, Wu NC, Mancuso N, Zelikovsky A, Sun R, Eskin E. PMID: 24932001; PMCID: PMC4058922.
      View in: PubMed   Mentions: 19     Fields:    Translation:Cells
    125. Allele-specific expression and eQTL analysis in mouse adipose tissue. BMC Genomics. 2014 Jun 13; 15:471. Hasin-Brumshtein Y, Hormozdiari F, Martin L, van Nas A, Eskin E, Lusis AJ, Drake TA. PMID: 24927774; PMCID: PMC4089026.
      View in: PubMed   Mentions: 34     Fields:    Translation:Animals
    126. Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies. Genome Biol. 2014 Apr 07; 15(4):r61. Joo JW, Sul JH, Han B, Ye C, Eskin E. PMID: 24708878; PMCID: PMC4053820.
      View in: PubMed   Mentions: 22     Fields:    Translation:AnimalsCells
    127. Identifying genetic relatives without compromising privacy. Genome Res. 2014 Apr; 24(4):664-72. He D, Furlotte NA, Hormozdiari F, Joo JW, Wadia A, Ostrovsky R, Sahai A, Eskin E. PMID: 24614977; PMCID: PMC3975065.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    128. Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysis. J Assoc Res Otolaryngol. 2014 Jun; 15(3):335-52. Ohmen J, Kang EY, Li X, Joo JW, Hormozdiari F, Zheng QY, Davis RC, Lusis AJ, Eskin E, Friedman RA. PMID: 24570207; PMCID: PMC4010595.
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    129. Genetic implication of a novel thiamine transporter in human hypertension. J Am Coll Cardiol. 2014 Apr 22; 63(15):1542-55. Zhang K, Huentelman MJ, Rao F, Sun EI, Corneveaux JJ, Schork AJ, Wei Z, Waalen J, Miramontes-Gonzalez JP, Hightower CM, Maihofer AX, Mahata M, Pastinen T, Ehret GB, International Consortium for Blood Pressure Genome-Wide Association Studies, Schork NJ, Eskin E, Nievergelt CM, Saier MH, O'Connor DT. PMID: 24509276; PMCID: PMC3992204.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    130. Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis. G3 (Bethesda). 2014 Jan 10; 4(1):121-31. Marsden CD, Lee Y, Kreppel K, Weakley A, Cornel A, Ferguson HM, Eskin E, Lanzaro GC. PMID: 24281424; PMCID: PMC3887528.
      View in: PubMed   Mentions: 19     Fields:    Translation:AnimalsPHPublic Health
    131. Meta-analysis identifies gene-by-environment interactions as demonstrated in a study of 4,965 mice. PLoS Genet. 2014 Jan; 10(1):e1004022. Kang EY, Han B, Furlotte N, Joo JW, Shih D, Davis RC, Lusis AJ, Eskin E. PMID: 24415945; PMCID: PMC3886926.
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    132. Fast pairwise IBD association testing in genome-wide association studies. Bioinformatics. 2014 Jan 15; 30(2):206-13. Han B, Kang EY, Raychaudhuri S, de Bakker PI, Eskin E. PMID: 24158599; PMCID: PMC3892684.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    133. eALPS: estimating abundance levels in pooled sequencing using available genotyping data. J Comput Biol. 2013 Nov; 20(11):861-77. Eskin I, Hormozdiari F, Conde L, Riby J, Skibola CF, Eskin E, Halperin E. PMID: 24144111; PMCID: PMC4013753.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    134. IPED: inheritance path-based pedigree reconstruction algorithm using genotype data. J Comput Biol. 2013 Oct; 20(10):780-91. He D, Wang Z, Han B, Parida L, Eskin E. PMID: 24093229; PMCID: PMC3791035.
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    135. Efficiently identifying significant associations in genome-wide association studies. J Comput Biol. 2013 Oct; 20(10):817-30. Kostem E, Eskin E. PMID: 24033261; PMCID: PMC3791046.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    136. Analysis of allele-specific expression in mouse liver by RNA-Seq: a comparison with Cis-eQTL identified using genetic linkage. Genetics. 2013 Nov; 195(3):1157-66. Lagarrigue S, Martin L, Hormozdiari F, Roux PF, Pan C, van Nas A, Demeure O, Cantor R, Ghazalpour A, Eskin E, Lusis AJ. PMID: 24026101; PMCID: PMC3813844.
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    137. Functional genomic assessment of phosgene-induced acute lung injury in mice. Am J Respir Cell Mol Biol. 2013 Sep; 49(3):368-83. Leikauf GD, Concel VJ, Bein K, Liu P, Berndt A, Martin TM, Ganguly K, Jang AS, Brant KA, Dopico RA, Upadhyay S, Cario C, Di YP, Vuga LJ, Kostem E, Eskin E, You M, Kaminski N, Prows DR, Knoell DL, Fabisiak JP. PMID: 23590305; PMCID: PMC3824050.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    138. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data. Bioinformatics. 2013 Sep 15; 29(18):2245-52. Yang WY, Hormozdiari F, Wang Z, He D, Pasaniuc B, Eskin E. PMID: 23825370; PMCID: PMC3753566.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    139. Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches. PLoS Genet. 2013 Jun; 9(6):e1003491. Sul JH, Han B, Ye C, Choi T, Eskin E. PMID: 23785294; PMCID: PMC3681686.
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    140. Rare variant association testing under low-coverage sequencing. Genetics. 2013 Jul; 194(3):769-79. Navon O, Sul JH, Han B, Conde L, Bracci PM, Riby J, Skibola CF, Eskin E, Halperin E. PMID: 23636738; PMCID: PMC3697979.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    141. Improving the accuracy and efficiency of partitioning heritability into the contributions of genomic regions. Am J Hum Genet. 2013 Apr 04; 92(4):558-64. Kostem E, Eskin E. PMID: 23561845; PMCID: PMC3617385.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    142. Mixed models can correct for population structure for genomic regions under selection. Nat Rev Genet. 2013 Apr; 14(4):300. Sul JH, Eskin E. PMID: 23438871.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    143. CNVeM: copy number variation detection using uncertainty of read mapping. J Comput Biol. 2013 Mar; 20(3):224-36. Wang Z, Hormozdiari F, Yang WY, Halperin E, Eskin E. PMID: 23421794; PMCID: PMC3590897.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    144. Genome-wide association mapping of blood cell traits in mice. Mamm Genome. 2013 Apr; 24(3-4):105-18. Davis RC, van Nas A, Bennett B, Orozco L, Pan C, Rau CD, Eskin E, Lusis AJ. PMID: 23417284; PMCID: PMC3933005.
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    145. Limited RNA editing in exons of mouse liver and adipose. Genetics. 2013 Apr; 193(4):1107-15. Lagarrigue S, Hormozdiari F, Martin LJ, Lecerf F, Hasin Y, Rau C, Hagopian R, Xiao Y, Yan J, Drake TA, Ghazalpour A, Eskin E, Lusis AJ. PMID: 23410828; PMCID: PMC3606090.
      View in: PubMed   Mentions: 15     Fields:    Translation:AnimalsCells
    146. Hap-seq: an optimal algorithm for haplotype phasing with imputation using sequencing data. J Comput Biol. 2013 Feb; 20(2):80-92. He D, Han B, Eskin E. PMID: 23383995; PMCID: PMC3576919.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    147. Genome reassembly with high-throughput sequencing data. BMC Genomics. 2013; 14 Suppl 1:S8. Parrish N, Sudakov B, Eskin E. PMID: 23368744; PMCID: PMC3549812.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    148. Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Mol Psychiatry. 2014 Feb; 19(2):228-34. Luykx JJ, Bakker SC, Lentjes E, Neeleman M, Strengman E, Mentink L, DeYoung J, de Jong S, Sul JH, Eskin E, van Eijk K, van Setten J, Buizer-Voskamp JE, Cantor RM, Lu A, van Amerongen M, van Dongen EP, Keijzers P, Kappen T, Borgdorff P, Bruins P, Derks EM, Kahn RS, Ophoff RA. PMID: 23319000.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    149. Genetic control of obesity and gut microbiota composition in response to high-fat, high-sucrose diet in mice. Cell Metab. 2013 Jan 08; 17(1):141-52. Parks BW, Nam E, Org E, Kostem E, Norheim F, Hui ST, Pan C, Civelek M, Rau CD, Bennett BJ, Mehrabian M, Ursell LK, He A, Castellani LW, Zinker B, Kirby M, Drake TA, Drevon CA, Knight R, Gargalovic P, Kirchgessner T, Eskin E, Lusis AJ. PMID: 23312289; PMCID: PMC3545283.
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    150. Systems genetic analysis of osteoblast-lineage cells. PLoS Genet. 2012; 8(12):e1003150. Calabrese G, Bennett BJ, Orozco L, Kang HM, Eskin E, Dombret C, De Backer O, Lusis AJ, Farber CR. PMID: 23300464; PMCID: PMC3531492.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansAnimalsCells
    151. Hap-seqX: expedite algorithm for haplotype phasing with imputation using sequence data. Gene. 2013 Apr 10; 518(1):2-6. He D, Eskin E. PMID: 23269365.
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    152. The Minnesota Center for Twin and Family Research genome-wide association study. Twin Res Hum Genet. 2012 Dec; 15(6):767-74. Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M. PMID: 23363460; PMCID: PMC3561927.
      View in: PubMed   Mentions: 58     Fields:    Translation:HumansCTClinical Trials
    153. Genome-wide association studies in mice. Nat Rev Genet. 2012 Nov; 13(11):807-17. Flint J, Eskin E. PMID: 23044826; PMCID: PMC3625632.
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    154. Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. Mamm Genome. 2012 Oct; 23(9-10):680-92. Ghazalpour A, Rau CD, Farber CR, Bennett BJ, Orozco LD, van Nas A, Pan C, Allayee H, Beaven SW, Civelek M, Davis RC, Drake TA, Friedman RA, Furlotte N, Hui ST, Jentsch JD, Kostem E, Kang HM, Kang EY, Joo JW, Korshunov VA, Laughlin RE, Martin LJ, Ohmen JD, Parks BW, Pellegrini M, Reue K, Smith DJ, Tetradis S, Wang J, Wang Y, Weiss JN, Kirchgessner T, Gargalovic PS, Eskin E, Lusis AJ, LeBoeuf RC. PMID: 22892838; PMCID: PMC3586763.
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    155. Genome-wide association study of Tourette's syndrome. Mol Psychiatry. 2013 Jun; 18(6):721-8. Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, Davis LK, Han B, Crane J, Moorjani P, Crenshaw AT, Parkin MA, Reus VI, Lowe TL, Rangel-Lugo M, Chouinard S, Dion Y, Girard S, Cath DC, Smit JH, King RA, Fernandez TV, Leckman JF, Kidd KK, Kidd JR, Pakstis AJ, State MW, Herrera LD, Romero R, Fournier E, Sandor P, Barr CL, Phan N, Gross-Tsur V, Benarroch F, Pollak Y, Budman CL, Bruun RD, Erenberg G, Naarden AL, Lee PC, Weiss N, Kremeyer B, Berrío GB, Campbell DD, Cardona Silgado JC, Ochoa WC, Mesa Restrepo SC, Muller H, Valencia Duarte AV, Lyon GJ, Leppert M, Morgan J, Weiss R, Grados MA, Anderson K, Davarya S, Singer H, Walkup J, Jankovic J, Tischfield JA, Heiman GA, Gilbert DL, Hoekstra PJ, Robertson MM, Kurlan R, Liu C, Gibbs JR, Singleton A, North American Brain Expression Consortium, Hardy J, UK Human Brain Expression Database, Strengman E, Ophoff RA, Wagner M, Moessner R, Mirel DB, Posthuma D, Sabatti C, Eskin E, Conti DV, Knowles JA, Ruiz-Linares A, Rouleau GA, Purcell S, Heutink P, Oostra BA, McMahon WM, Freimer NB, Cox NJ, Pauls DL. PMID: 22889924; PMCID: PMC3605224.
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    156. "Good enough solutions" and the genetics of complex diseases. Circ Res. 2012 Aug 03; 111(4):493-504. Weiss JN, Karma A, MacLellan WR, Deng M, Rau CD, Rees CM, Wang J, Wisniewski N, Eskin E, Horvath S, Qu Z, Wang Y, Lusis AJ. PMID: 22859671; PMCID: PMC3428228.
      View in: PubMed   Mentions: 54     Fields:    Translation:HumansAnimals
    157. Mapping genetic variants associated with beta-adrenergic responses in inbred mice. PLoS One. 2012; 7(7):e41032. Hersch M, Peter B, Kang HM, Schüpfer F, Abriel H, Pedrazzini T, Eskin E, Beckmann JS, Bergmann S, Maurer F. PMID: 22859963; PMCID: PMC3409184.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    158. High-resolution association mapping of atherosclerosis loci in mice. Arterioscler Thromb Vasc Biol. 2012 Aug; 32(8):1790-8. Bennett BJ, Orozco L, Kostem E, Erbilgin A, Dallinga M, Neuhaus I, Guan B, Wang X, Eskin E, Lusis AJ. PMID: 22723443; PMCID: PMC3519423.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    159. Incorporating prior information into association studies. Bioinformatics. 2012 Jun 15; 28(12):i147-53. Darnell G, Duong D, Han B, Eskin E. PMID: 22689754; PMCID: PMC3371867.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    160. Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome. Circ Cardiovasc Genet. 2012 Aug 01; 5(4):430-40. Friese RS, Ye C, Nievergelt CM, Schork AJ, Mahapatra NR, Rao F, Napolitan PS, Waalen J, Ehret GB, Munroe PB, Schmid-Schönbein GW, Eskin E, O'Connor DT. PMID: 22670052; PMCID: PMC3467001.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    161. Improved linear mixed models for genome-wide association studies. Nat Methods. 2012 May 30; 9(6):525-6. Listgarten J, Lippert C, Kadie CM, Davidson RI, Eskin E, Heckerman D. PMID: 22669648; PMCID: PMC3597090.
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    162. A model-based approach for analysis of spatial structure in genetic data. Nat Genet. 2012 May 20; 44(6):725-31. Yang WY, Novembre J, Eskin E, Halperin E. PMID: 22610118; PMCID: PMC3592563.
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    163. Genome-wide association mapping with longitudinal data. Genet Epidemiol. 2012 Jul; 36(5):463-71. Furlotte NA, Eskin E, Eyheramendy S. PMID: 22581622; PMCID: PMC3625633.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    164. Increasing association mapping power and resolution in mouse genetic studies through the use of meta-analysis for structured populations. Genetics. 2012 Jul; 191(3):959-67. Furlotte NA, Kang EY, Van Nas A, Farber CR, Lusis AJ, Eskin E. PMID: 22505625; PMCID: PMC3389987.
      View in: PubMed   Mentions: 9     Fields:    Translation:Animals
    165. Interpreting meta-analyses of genome-wide association studies. PLoS Genet. 2012; 8(3):e1002555. Han B, Eskin E. PMID: 22396665; PMCID: PMC3291559.
      View in: PubMed   Mentions: 93     Fields:    Translation:Humans
    166. Fatigue risk management in the workplace. J Occup Environ Med. 2012 Feb; 54(2):231-58. Lerman SE, Eskin E, Flower DJ, George EC, Gerson B, Hartenbaum N, Hursh SR, Moore-Ede M, American College of Occupational and Environmental Medicine Presidential Task Force on Fatigue Risk . PMID: 22269988.
      View in: PubMed   Mentions: 56     Fields:    Translation:Humans
    167. Increasing power of groupwise association test with likelihood ratio test. J Comput Biol. 2011 Nov; 18(11):1611-24. Sul JH, Han B, Eskin E. PMID: 21919745; PMCID: PMC3216097.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    168. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature. 2011 Sep 14; 477(7364):289-94. Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, Heger A, Agam A, Slater G, Goodson M, Furlotte NA, Eskin E, Nellåker C, Whitley H, Cleak J, Janowitz D, Hernandez-Pliego P, Edwards A, Belgard TG, Oliver PL, McIntyre RE, Bhomra A, Nicod J, Gan X, Yuan W, van der Weyden L, Steward CA, Bala S, Stalker J, Mott R, Durbin R, Jackson IJ, Czechanski A, Guerra-Assunção JA, Donahue LR, Reinholdt LG, Payseur BA, Ponting CP, Birney E, Flint J, Adams DJ. PMID: 21921910; PMCID: PMC3276836.
      View in: PubMed   Mentions: 962     Fields:    Translation:Animals
    169. Assembly of non-unique insertion content using next-generation sequencing. BMC Bioinformatics. 2011; 12 Suppl 6:S3. Parrish N, Hormozdiari F, Eskin E. PMID: 21989261; PMCID: PMC3194191.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    170. Genotyping common and rare variation using overlapping pool sequencing. BMC Bioinformatics. 2011; 12 Suppl 6:S2. He D, Zaitlen N, Pasaniuc B, Eskin E, Halperin E. PMID: 21989232; PMCID: PMC3194190.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    171. Mixed-model coexpression: calculating gene coexpression while accounting for expression heterogeneity. Bioinformatics. 2011 Jul 01; 27(13):i288-94. Furlotte NA, Kang HM, Ye C, Eskin E. PMID: 21685083; PMCID: PMC3117390.
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    172. Comparative analysis of proteome and transcriptome variation in mouse. PLoS Genet. 2011 Jun; 7(6):e1001393. Ghazalpour A, Bennett B, Petyuk VA, Orozco L, Hagopian R, Mungrue IN, Farber CR, Sinsheimer J, Kang HM, Furlotte N, Park CC, Wen PZ, Brewer H, Weitz K, Camp DG, Pan C, Yordanova R, Neuhaus I, Tilford C, Siemers N, Gargalovic P, Eskin E, Kirchgessner T, Smith DJ, Smith RD, Lusis AJ. PMID: 21695224; PMCID: PMC3111477.
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    173. Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. Am J Hum Genet. 2011 May 13; 88(5):586-98. Han B, Eskin E. PMID: 21565292; PMCID: PMC3146723.
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    174. Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. PLoS Genet. 2011 Apr; 7(4):e1001383. Van Tyne D, Park DJ, Schaffner SF, Neafsey DE, Angelino E, Cortese JF, Barnes KG, Rosen DM, Lukens AK, Daniels RF, Milner DA, Johnson CA, Shlyakhter I, Grossman SR, Becker JS, Yamins D, Karlsson EK, Ndiaye D, Sarr O, Mboup S, Happi C, Furlotte NA, Eskin E, Kang HM, Hartl DL, Birren BW, Wiegand RC, Lander ES, Wirth DF, Volkman SK, Sabeti PC. PMID: 21533027; PMCID: PMC3080868.
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    175. Efficient algorithms for tandem copy number variation reconstruction in repeat-rich regions. Bioinformatics. 2011 Jun 01; 27(11):1513-20. He D, Hormozdiari F, Furlotte N, Eskin E. PMID: 21505028; PMCID: PMC3102223.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    176. Mouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesis. PLoS Genet. 2011 Apr; 7(4):e1002038. Farber CR, Bennett BJ, Orozco L, Zou W, Lira A, Kostem E, Kang HM, Furlotte N, Berberyan A, Ghazalpour A, Suwanwela J, Drake TA, Eskin E, Wang QT, Teitelbaum SL, Lusis AJ. PMID: 21490954; PMCID: PMC3072371.
      View in: PubMed   Mentions: 85     Fields:    Translation:AnimalsCells
    177. Increasing power of genome-wide association studies by collecting additional single-nucleotide polymorphisms. Genetics. 2011 Jun; 188(2):449-60. Kostem E, Lozano JA, Eskin E. PMID: 21467568; PMCID: PMC3122306.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    178. Gene networks associated with conditional fear in mice identified using a systems genetics approach. BMC Syst Biol. 2011 Mar 16; 5:43. Park CC, Gale GD, de Jong S, Ghazalpour A, Bennett BJ, Farber CR, Langfelder P, Lin A, Khan AH, Eskin E, Horvath S, Lusis AJ, Ophoff RA, Smith DJ. PMID: 21410935; PMCID: PMC3070648.
      View in: PubMed   Mentions: 55     Fields:    Translation:AnimalsCells
    179. An optimal weighted aggregated association test for identification of rare variants involved in common diseases. Genetics. 2011 May; 188(1):181-8. Sul JH, Han B, He D, Eskin E. PMID: 21368279; PMCID: PMC3120154.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    180. Postassociation cleaning using linkage disequilibrium information. Genet Epidemiol. 2011 Jan; 35(1):1-10. Han B, Hackel BM, Eskin E. PMID: 21181893.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    181. Detection and reconstruction of tandemly organized de novo copy number variations. BMC Bioinformatics. 2010 Dec 14; 11 Suppl 11:S12. He D, Furlotte N, Eskin E. PMID: 21172047; PMCID: PMC3024866.
      View in: PubMed   Mentions: 4     Fields:    Translation:Animals
    182. Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population. Hum Mol Genet. 2011 Feb 15; 20(4):827-39. Kenny EE, Kim M, Gusev A, Lowe JK, Salit J, Smith JG, Kovvali S, Kang HM, Newton-Cheh C, Daly MJ, Stoffel M, Altshuler DM, Friedman JM, Eskin E, Breslow JL, Pe'er I. PMID: 21118897; PMCID: PMC3024042.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    183. In silico QTL mapping of basal liver iron levels in inbred mouse strains. Physiol Genomics. 2011 Feb 11; 43(3):136-47. McLachlan S, Lee SM, Steele TM, Hawthorne PL, Zapala MA, Eskin E, Schork NJ, Anderson GJ, Vulpe CD. PMID: 21062905; PMCID: PMC3055709.
      View in: PubMed   Mentions: 13     Fields:    Translation:Animals
    184. Imputation aware meta-analysis of genome-wide association studies. Genet Epidemiol. 2010 Sep; 34(6):537-42. Zaitlen N, Eskin E. PMID: 20717975; PMCID: PMC3102182.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    185. Multi-marker tagging single nucleotide polymorphism selection using estimation of distribution algorithms. Artif Intell Med. 2010 Nov; 50(3):193-201. Santana R, Mendiburu A, Zaitlen N, Eskin E, Lozano JA. PMID: 20650616.
      View in: PubMed   Mentions: 2     Fields:    
    186. Optimal algorithms for haplotype assembly from whole-genome sequence data. Bioinformatics. 2010 Jun 15; 26(12):i183-90. He D, Choi A, Pipatsrisawat K, Darwiche A, Eskin E. PMID: 20529904; PMCID: PMC2881399.
      View in: PubMed   Mentions: 46     Fields:    Translation:Cells
    187. Genome-wide case/control studies in hypertension: only the 'tip of the iceberg'. J Hypertens. 2010 Jun; 28(6):1115-23. Zhang K, Weder AB, Eskin E, O'Connor DT. PMID: 20216088; PMCID: PMC2873167.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    188. Fine mapping in 94 inbred mouse strains using a high-density haplotype resource. Genetics. 2010 Jul; 185(3):1081-95. Kirby A, Kang HM, Wade CM, Cotsapas C, Kostem E, Han B, Furlotte N, Kang EY, Rivas M, Bogue MA, Frazer KA, Johnson FM, Beilharz EJ, Cox DR, Eskin E, Daly MJ. PMID: 20439770; PMCID: PMC2907194.
      View in: PubMed   Mentions: 74     Fields:    Translation:HumansAnimals
    189. Variance component model to account for sample structure in genome-wide association studies. Nat Genet. 2010 Apr; 42(4):348-54. Kang HM, Sul JH, Service SK, Zaitlen NA, Kong SY, Freimer NB, Sabatti C, Eskin E. PMID: 20208533; PMCID: PMC3092069.
      View in: PubMed   Mentions: 1327     Fields:    Translation:Humans
    190. EMINIM: an adaptive and memory-efficient algorithm for genotype imputation. J Comput Biol. 2010 Mar; 17(3):547-60. Kang HM, Zaitlen NA, Eskin E. PMID: 20377463; PMCID: PMC3198882.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimals
    191. Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage. 2010 Jun; 51(2):542-54. Stein JL, Hua X, Morra JH, Lee S, Hibar DP, Ho AJ, Leow AD, Toga AW, Sul JH, Kang HM, Eskin E, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, Stephan DA, Webster J, DeChairo BM, Potkin SG, Jack CR, Weiner MW, Thompson PM, Alzheimer's Disease Neuroimaging Initiative. PMID: 20197096; PMCID: PMC2856746.
      View in: PubMed   Mentions: 97     Fields:    Translation:Humans
    192. Detecting the presence and absence of causal relationships between expression of yeast genes with very few samples. J Comput Biol. 2010 Mar; 17(3):533-46. Kang EY, Ye C, Shpitser I, Eskin E. PMID: 20377462; PMCID: PMC3198891.
      View in: PubMed   Mentions: 5     Fields:    Translation:Animals
    193. A high-resolution association mapping panel for the dissection of complex traits in mice. Genome Res. 2010 Feb; 20(2):281-90. Bennett BJ, Farber CR, Orozco L, Kang HM, Ghazalpour A, Siemers N, Neubauer M, Neuhaus I, Yordanova R, Guan B, Truong A, Yang WP, He A, Kayne P, Gargalovic P, Kirchgessner T, Pan C, Castellani LW, Kostem E, Furlotte N, Drake TA, Eskin E, Lusis AJ. PMID: 20054062; PMCID: PMC2813484.
      View in: PubMed   Mentions: 213     Fields:    Translation:Animals
    194. Identification of novel genes that mediate innate immunity using inbred mice. Genetics. 2009 Dec; 183(4):1535-44. Yang IV, Wade CM, Kang HM, Alper S, Rutledge H, Lackford B, Eskin E, Daly MJ, Schwartz DA. PMID: 19805818; PMCID: PMC2787437.
      View in: PubMed   Mentions: 38     Fields:    Translation:AnimalsCells
    195. Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs. J Pharmacol Exp Ther. 2009 Nov; 331(2):419-28. Rana BK, Wessel J, Mahboubi V, Rao F, Haeller J, Gayen JR, Eskin E, Valle AM, Das M, Mahata SK, Taupenot L, Stridsberg M, Talley TT, Ziegler MG, Smith DW, Schork NJ, O'Connor DT, Taylor P. PMID: 19671882; PMCID: PMC2775266.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    196. Genome-wide association study of bipolar disorder in European American and African American individuals. Mol Psychiatry. 2009 Aug; 14(8):755-63. Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, Koller DL, Lawson WB, Liu C, Lohoff F, McInnis MG, McMahon FJ, Mirel DB, Murray SS, Nievergelt C, Nurnberger J, Nwulia EA, Paschall J, Potash JB, Rice J, Schulze TG, Scheftner W, Panganiban C, Zaitlen N, Zandi PP, Zöllner S, Schork NJ, Kelsoe JR. PMID: 19488044; PMCID: PMC3035981.
      View in: PubMed   Mentions: 195     Fields:    Translation:Humans
    197. Rapid and accurate multiple testing correction and power estimation for millions of correlated markers. PLoS Genet. 2009 Apr; 5(4):e1000456. Han B, Kang HM, Eskin E. PMID: 19381255; PMCID: PMC2663787.
      View in: PubMed   Mentions: 87     Fields:    Translation:Humans
    198. Linkage effects and analysis of finite sample errors in the HapMap. Hum Hered. 2009; 68(2):73-86. Zaitlen N, Kang HM, Eskin E. PMID: 19365134; PMCID: PMC2874737.
      View in: PubMed   Mentions: 4     Fields:    
    199. Using network component analysis to dissect regulatory networks mediated by transcription factors in yeast. PLoS Comput Biol. 2009 Mar; 5(3):e1000311. Ye C, Galbraith SJ, Liao JC, Eskin E. PMID: 19300475; PMCID: PMC2649002.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    200. Accurate discovery of expression quantitative trait loci under confounding from spurious and genuine regulatory hotspots. Genetics. 2008 Dec; 180(4):1909-25. Kang HM, Ye C, Eskin E. PMID: 18791227; PMCID: PMC2600931.
      View in: PubMed   Mentions: 83     Fields:    Translation:HumansAnimals
    201. Efficient association study design via power-optimized tag SNP selection. Ann Hum Genet. 2008 Nov; 72(Pt 6):834-47. Han B, Kang HM, Seo MS, Zaitlen N, Eskin E. PMID: 18702637; PMCID: PMC2574965.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    202. High-resolution mapping of gene expression using association in an outbred mouse stock. PLoS Genet. 2008 Aug 08; 4(8):e1000149. Ghazalpour A, Doss S, Kang H, Farber C, Wen PZ, Brozell A, Castellanos R, Eskin E, Smith DJ, Drake TA, Lusis AJ. PMID: 18688273; PMCID: PMC2483929.
      View in: PubMed   Mentions: 42     Fields:    Translation:AnimalsCells
    203. Increasing power in association studies by using linkage disequilibrium structure and molecular function as prior information. Genome Res. 2008 Apr; 18(4):653-60. Eskin E. PMID: 18353808; PMCID: PMC2279252.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    204. Efficient control of population structure in model organism association mapping. Genetics. 2008 Mar; 178(3):1709-23. Kang HM, Zaitlen NA, Wade CM, Kirby A, Heckerman D, Daly MJ, Eskin E. PMID: 18385116; PMCID: PMC2278096.
      View in: PubMed   Mentions: 822     Fields:    Translation:Animals
    205. Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping. BMC Genet. 2008 Feb 05; 9:14. Olshen AB, Gold B, Lohmueller KE, Struewing JP, Satagopan J, Stefanov SA, Eskin E, Kirchhoff T, Lautenberger JA, Klein RJ, Friedman E, Norton L, Ellis NA, Viale A, Lee CS, Borgen PI, Clark AG, Offit K, Boyd J. PMID: 18251999; PMCID: PMC2259380.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    206. Further evidence for association of GRK3 to bipolar disorder suggests a second disease mutation. Psychiatr Genet. 2007 Dec; 17(6):315-22. Barrett TB, Emberton JE, Nievergelt CM, Liang SG, Hauger RL, Eskin E, Schork NJ, Kelsoe JR. PMID: 18075471.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    207. A sequence-based variation map of 8.27 million SNPs in inbred mouse strains. Nature. 2007 Aug 30; 448(7157):1050-3. Frazer KA, Eskin E, Kang HM, Bogue MA, Hinds DA, Beilharz EJ, Gupta RV, Montgomery J, Morenzoni MM, Nilsen GB, Pethiyagoda CL, Stuve LL, Johnson FM, Daly MJ, Wade CM, Cox DR. PMID: 17660834.
      View in: PubMed   Mentions: 266     Fields:    Translation:AnimalsCells
    208. Incorporating homologues into sequence embeddings for protein analysis. J Bioinform Comput Biol. 2007 Jun; 5(3):717-38. Eskin E, Snir S. PMID: 17688313.
      View in: PubMed   Mentions: 2     Fields:    Translation:Cells
    209. Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension. Circulation. 2007 May 01; 115(17):2271-81. Rao F, Wen G, Gayen JR, Das M, Vaingankar SM, Rana BK, Mahata M, Kennedy BP, Salem RM, Stridsberg M, Abel K, Smith DW, Eskin E, Schork NJ, Hamilton BA, Ziegler MG, Mahata SK, O'Connor DT. PMID: 17438154.
      View in: PubMed   Mentions: 57     Fields:    Translation:HumansCells
    210. Leveraging the HapMap correlation structure in association studies. Am J Hum Genet. 2007 Apr; 80(4):683-91. Zaitlen N, Kang HM, Eskin E, Halperin E. PMID: 17357074; PMCID: PMC1852710.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    211. Discovering tightly regulated and differentially expressed gene sets in whole genome expression data. Bioinformatics. 2007 Jan 15; 23(2):e84-90. Ye C, Eskin E. PMID: 17237110.
      View in: PubMed   Mentions: 8     Fields:    
    212. A note on phasing long genomic regions using local haplotype predictions. J Bioinform Comput Biol. 2006 Jun; 4(3):639-47. Eskin E, Sharan R, Halperin E. PMID: 16960967.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    213. Discrete profile comparison using information bottleneck. BMC Bioinformatics. 2006 Mar 20; 7 Suppl 1:S8. O'Rourke S, Chechik G, Friedman R, Eskin E. PMID: 16723011; PMCID: PMC1810319.
      View in: PubMed   Mentions:    Fields:    Translation:Cells
    214. Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples. Mol Psychiatry. 2006 Feb; 11(2):125-33, 115. Greenwood TA, Schork NJ, Eskin E, Kelsoe JR. PMID: 16261167.
      View in: PubMed   Mentions: 63     Fields:    Translation:HumansCellsCTClinical Trials
    215. A comparison of phasing algorithms for trios and unrelated individuals. Am J Hum Genet. 2006 Mar; 78(3):437-50. Marchini J, Cutler D, Patterson N, Stephens M, Eskin E, Halperin E, Lin S, Qin ZS, Munro HM, Abecasis GR, Donnelly P, International HapMap Consortium. PMID: 16465620; PMCID: PMC1380287.
      View in: PubMed   Mentions: 133     Fields:    Translation:Humans
    216. Polymorphisms and haplotypes of the regulator of G protein signaling-2 gene in normotensives and hypertensives. Hypertension. 2006 Mar; 47(3):415-20. Riddle EL, Rana BK, Murthy KK, Rao F, Eskin E, O'Connor DT, Insel PA. PMID: 16432041.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    217. Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP. Genome Res. 2005 Nov; 15(11):1594-600. Zaitlen NA, Kang HM, Feolo ML, Sherry ST, Halperin E, Eskin E. PMID: 16251470; PMCID: PMC1310648.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimals
    218. Searching genomes for noncoding RNA using FastR. IEEE/ACM Trans Comput Biol Bioinform. 2005 Oct-Dec; 2(4):366-79. Zhang S, Haas B, Eskin E, Bafna V. PMID: 17044173.
      View in: PubMed   Mentions: 17     Fields:    Translation:AnimalsCells
    219. Whole-genome patterns of common DNA variation in three human populations. Science. 2005 Feb 18; 307(5712):1072-9. Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR. PMID: 15718463.
      View in: PubMed   Mentions: 450     Fields:    Translation:Humans
    220. Assessing computational tools for the discovery of transcription factor binding sites. Nat Biotechnol. 2005 Jan; 23(1):137-44. Tompa M, Li N, Bailey TL, Church GM, De Moor B, Eskin E, Favorov AV, Frith MC, Fu Y, Kent WJ, Makeev VJ, Mironov AA, Noble WS, Pavesi G, Pesole G, Régnier M, Simonis N, Sinha S, Thijs G, van Helden J, Vandenbogaert M, Weng Z, Workman C, Ye C, Zhu Z. PMID: 15637633.
      View in: PubMed   Mentions: 446     Fields:    Translation:HumansAnimalsCells
    221. Whole-genome analysis of Alu repeat elements reveals complex evolutionary history. Genome Res. 2004 Nov; 14(11):2245-52. Price AL, Eskin E, Pevzner PA. PMID: 15520288; PMCID: PMC525682.
      View in: PubMed   Mentions: 105     Fields:    Translation:HumansCells
    222. Haplotype reconstruction from genotype data using Imperfect Phylogeny. Bioinformatics. 2004 Aug 12; 20(12):1842-9. Halperin E, Eskin E. PMID: 14988101.
      View in: PubMed   Mentions: 67     Fields:    
    223. Mismatch string kernels for discriminative protein classification. Bioinformatics. 2004 Mar 01; 20(4):467-76. Leslie CS, Eskin E, Cohen A, Weston J, Noble WS. PMID: 14990442.
      View in: PubMed   Mentions: 122     Fields:    Translation:Cells
    224. Combining text mining and sequence analysis to discover protein functional regions. Pac Symp Biocomput. 2004; 288-99. Eskin E, Agichtein E. PMID: 14992511.
      View in: PubMed   Mentions: 3     Fields:    
    225. Efficient reconstruction of haplotype structure via perfect phylogeny. J Bioinform Comput Biol. 2003 Apr; 1(1):1-20. Eskin E, Halperin E, Karp RM. PMID: 15290779.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    226. Protein family classification using sparse markov transducers. J Comput Biol. 2003; 10(2):187-213. Eskin E, Noble WS, Singer Y. PMID: 12804091.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    227. Genome-wide analysis of bacterial promoter regions. Pac Symp Biocomput. 2003; 29-40. Eskin E, Keich U, Gelfand MS, Pevzner PA. PMID: 12603015.
      View in: PubMed   Mentions: 11     Fields:    Translation:Cells
    228. The spectrum kernel: a string kernel for SVM protein classification. Pac Symp Biocomput. 2002; 564-75. Leslie C, Eskin E, Noble WS. PMID: 11928508.
      View in: PubMed   Mentions: 148     Fields:    
    229. Using substitution matrices to estimate probability distributions for biological sequences. J Comput Biol. 2002; 9(6):775-91. Eskin E, Noble WS, Singer Y. PMID: 12614546.
      View in: PubMed   Mentions: 1     Fields:    Translation:Cells
    230. Finding composite regulatory patterns in DNA sequences. Bioinformatics. 2002; 18 Suppl 1:S354-63. Eskin E, Pevzner PA. PMID: 12169566.
      View in: PubMed   Mentions: 70     Fields:    Translation:Cells
    231. Using mixtures of common ancestors for estimating the probabilities of discrete events in biological sequences. Bioinformatics. 2001; 17 Suppl 1:S65-73. Eskin E, Grundy WN, Singer Y. PMID: 11472994.
      View in: PubMed   Mentions:    Fields:    Translation:Cells
    232. Protein family classification using sparse Markov transducers. Proc Int Conf Intell Syst Mol Biol. 2000; 8:134-45. Eskin E, Grundy WN, Singer Y. PMID: 10977074.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    233. Increasing accuracy in the diagnosis of acute appendicitis with modern diagnostic techniques. Am Surg. 1986 Apr; 52(4):222-5. Kniskern JH, Eskin EM, Fletcher HS. PMID: 3513683.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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