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Genetic variants of glucose metabolism and exposure to smoking in African American breast cancer. Endocr Relat Cancer. 2023 04 01; 30(4).
Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H. PMID: 36705562; PMCID: PMC10095926.
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PubMed Mentions: Fields:
Translation:
Humans
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Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. Am J Hum Genet. 2023 02 02; 110(2):314-325.
Ko S, Chu BB, Peterson D, Okenwa C, Papp JC, Alexander DH, Sobel EM, Zhou H, Lange KL. PMID: 36610401; PMCID: PMC9943729.
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PubMed Mentions: Fields:
Translation:
Humans
-
A fast data-driven method for genotype imputation, phasing and local ancestry inference: MendelImpute.jl. Bioinformatics. 2021 12 11; 37(24):4756-4763.
Chu BB, Sobel EM, Wasiolek R, Ko S, Sinsheimer JS, Zhou H, Lange K. PMID: 34289008; PMCID: PMC8665755.
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PubMed Mentions:
2 Fields:
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Synergistic Effects of Genetic Variants of Glucose Homeostasis and Lifelong Exposures to Cigarette Smoking, Female Hormones, and Dietary Fat Intake on Primary Colorectal Cancer Development in African and Hispanic/Latino American Women. Front Oncol. 2021; 11:760243.
Jung SY, Sobel EM, Pellegrini M, Yu H, Papp JC. PMID: 34692549; PMCID: PMC8529283.
View in:
PubMed Mentions:
1
-
Molecular Biology Networks and Key Gene Regulators for Inflammatory Biomarkers Shared by Breast Cancer Development: Multi-Omics Systems Analysis. Biomolecules. 2021 09 18; 11(9).
Jung SY, Papp JC, Pellegrini M, Yu H, Sobel EM. PMID: 34572592; PMCID: PMC8469138.
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PubMed Mentions:
2 Fields:
Translation:
HumansCells
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Modern simulation utilities for genetic analysis. BMC Bioinformatics. 2021 May 03; 22(1):228.
Ji SS, German CA, Lange K, Sinsheimer JS, Zhou H, Zhou J, Sobel EM. PMID: 33941078; PMCID: PMC8091532.
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PubMed Mentions:
2 Fields:
Translation:
Humans
-
Genetically determined elevated C-reactive protein associated with primary colorectal cancer risk: Mendelian randomization with lifestyle interactions. Am J Cancer Res. 2021; 11(4):1733-1753.
Jung SY, Yu H, Pellegrini M, Papp JC, Sobel EM, Zhang ZF. PMID: 33948386; PMCID: PMC8085861.
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PubMed Mentions:
3
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Genetically Predicted C-Reactive Protein Associated With Postmenopausal Breast Cancer Risk: Interrelation With Estrogen and Cancer Molecular Subtypes Using Mendelian Randomization. Front Oncol. 2020; 10:630994.
Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H, Zhang ZF. PMID: 33614510; PMCID: PMC7888276.
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PubMed Mentions:
3
-
Pro-inflammatory cytokine polymorphisms and interactions with dietary alcohol and estrogen, risk factors for invasive breast cancer using a post genome-wide analysis for gene-gene and gene-lifestyle interaction. Sci Rep. 2021 01 13; 11(1):1058.
Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H, Zhang ZF. PMID: 33441805; PMCID: PMC7807068.
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PubMed Mentions:
5 Fields:
Translation:
Humans
-
Genome-wide Association Analysis of Proinflammatory Cytokines and Gene-lifestyle Interaction for Invasive Breast Cancer Risk: The WHI dbGaP Study. Cancer Prev Res (Phila). 2021 01; 14(1):41-54.
Jung SY, Scott PA, Papp JC, Sobel EM, Pellegrini M, Yu H, Han S, Zhang ZF. PMID: 32928877; PMCID: PMC7956151.
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PubMed Mentions:
10 Fields:
Translation:
HumansCells
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Pro-inflammatory cytokine polymorphisms in ONECUT2 and HNF4A and primary colorectal carcinoma: a post genome-wide gene-lifestyle interaction study. Am J Cancer Res. 2020; 10(9):2955-2976.
Jung SY, Papp JC, Sobel EM, Pellegrini M, Yu H, Zhang ZF. PMID: 33042629; PMCID: PMC7539781.
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PubMed Mentions:
3
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Mendelian Randomization Study: The Association Between Metabolic Pathways and Colorectal Cancer Risk. Front Oncol. 2020; 10:1005.
Jung SY, Papp JC, Sobel EM, Zhang ZF. PMID: 32850306; PMCID: PMC7396568.
View in:
PubMed Mentions:
5
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Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity. Gigascience. 2020 06 01; 9(6).
Chu BB, Keys KL, German CA, Zhou H, Zhou JJ, Sobel EM, Sinsheimer JS, Lange K. PMID: 32491161; PMCID: PMC7268817.
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PubMed Mentions:
9 Fields:
Translation:
Humans
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Post Genome-Wide Gene-Environment Interaction Study Using Random Survival Forest: Insulin Resistance, Lifestyle Factors, and Colorectal Cancer Risk. Cancer Prev Res (Phila). 2019 12; 12(12):877-890.
Jung SY, Papp JC, Sobel EM, Zhang ZF. PMID: 31554631; PMCID: PMC6893139.
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PubMed Mentions:
2 Fields:
Translation:
Humans
-
Post genome-wide gene-environment interaction study: The effect of genetically driven insulin resistance on breast cancer risk using Mendelian randomization. PLoS One. 2019; 14(6):e0218917.
Jung SY, Mancuso N, Papp J, Sobel E, Zhang ZF. PMID: 31246991; PMCID: PMC6597082.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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Breast Cancer Risk and Insulin Resistance: Post Genome-Wide Gene-Environment Interaction Study Using a Random Survival Forest. Cancer Res. 2019 05 15; 79(10):2784-2794.
Jung SY, Papp JC, Sobel EM, Yu H, Zhang ZF. PMID: 30936085; PMCID: PMC6522308.
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PubMed Mentions:
10 Fields:
Translation:
Humans
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OPENMENDEL: a cooperative programming project for statistical genetics. Hum Genet. 2020 Jan; 139(1):61-71.
Zhou H, Sinsheimer JS, Bates DM, Chu BB, German CA, Ji SS, Keys KL, Kim J, Ko S, Mosher GD, Papp JC, Sobel EM, Zhai J, Zhou JJ, Lange K. PMID: 30915546; PMCID: PMC6763373.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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Genome-Wide Meta-analysis of Gene-Environmental Interaction for Insulin Resistance Phenotypes and Breast Cancer Risk in Postmenopausal Women. Cancer Prev Res (Phila). 2019 01; 12(1):31-42.
Jung SY, Mancuso N, Yu H, Papp J, Sobel E, Zhang ZF. PMID: 30327367.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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Genetic Variants in Metabolic Signaling Pathways and Their Interaction with Lifestyle Factors on Breast Cancer Risk: A Random Survival Forest Analysis. Cancer Prev Res (Phila). 2018 01; 11(1):44-51.
Jung SY, Papp JC, Sobel EM, Zhang ZF. PMID: 29074537; PMCID: PMC5754228.
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PubMed Mentions:
3 Fields:
Translation:
HumansCells
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Interaction of insulin-like growth factor-I and insulin resistance-related genetic variants with lifestyle factors on postmenopausal breast cancer risk. Breast Cancer Res Treat. 2017 Jul; 164(2):475-495.
Jung SY, Ho G, Rohan T, Strickler H, Bea J, Papp J, Sobel E, Zhang ZF, Crandall C. PMID: 28478612.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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Effect of genetic variants and traits related to glucose metabolism and their interaction with obesity on breast and colorectal cancer risk among postmenopausal women. BMC Cancer. 2017 04 26; 17(1):290.
Jung SY, Sobel EM, Papp JC, Zhang ZF. PMID: 28446149; PMCID: PMC5405540.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes. Hum Hered. 2016; 81(4):181-193.
Clark MM, Chazara O, Sobel EM, Gjessing HK, Magnus P, Moffett A, Sinsheimer JS. PMID: 28214848; PMCID: PMC5557278.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data. Genet Epidemiol. 2017 04; 41(3):174-186.
Zhou H, Blangero J, Dyer TD, Chan KK, Lange K, Sobel EM. PMID: 27943406; PMCID: PMC5340631.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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Genome-wide QTL and eQTL analyses using Mendel. BMC Proc. 2016; 10(Suppl 7):239-244.
Zhou H, Zhou J, Hu T, Sobel EM, Lange K. PMID: 27980643; PMCID: PMC5133530.
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PubMed Mentions:
1
-
Obesity and associated lifestyles modify the effect of glucose metabolism-related genetic variants on impaired glucose homeostasis among postmenopausal women. Genet Epidemiol. 2016 09; 40(6):520-30.
Jung SY, Sobel EM, Papp JC, Crandall CJ, Fu AN, Zhang ZF. PMID: 27377425; PMCID: PMC5560051.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions. Ann Hum Genet. 2016 Jan; 80(1):63-80.
Clark MM, Blangero J, Dyer TD, Sobel EM, Sinsheimer JS. PMID: 26567478; PMCID: PMC4715557.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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Genome-wide ultraconserved elements exhibit higher phylogenetic informativeness than traditional gene markers in percomorph fishes. Mol Phylogenet Evol. 2015 Nov; 92:140-6.
Gilbert PS, Chang J, Pan C, Sobel EM, Sinsheimer JS, Faircloth BC, Alfaro ME. PMID: 26079130; PMCID: PMC4583375.
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PubMed Mentions:
24 Fields:
Translation:
AnimalsCells
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Shared molecular pathways and gene networks for cardiovascular disease and type 2 diabetes mellitus in women across diverse ethnicities. Circ Cardiovasc Genet. 2014 Dec; 7(6):911-9.
Chan KH, Huang YT, Meng Q, Wu C, Reiner A, Sobel EM, Tinker L, Lusis AJ, Yang X, Liu S. PMID: 25371518.
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PubMed Mentions:
30 Fields:
Translation:
Humans
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Fast genome-wide pedigree quantitative trait loci analysis using MENDEL. BMC Proc. 2014; 8(Suppl 1):S93.
Zhou H, Zhou J, Sobel EM, Lange K. PMID: 25519348; PMCID: PMC4143629.
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PubMed Mentions:
3
-
Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data. Annu Rev Stat Appl. 2014 Jan 01; 1(1):279-300.
Lange K, Papp JC, Sinsheimer JS, Sobel EM. PMID: 24955378; PMCID: PMC4062304.
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PubMed Mentions:
15
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The systems genetics resource: a web application to mine global data for complex disease traits. Front Genet. 2013; 4:84.
van Nas A, Pan C, Ingram-Drake LA, Ghazalpour A, Drake TA, Sobel EM, Papp JC, Lusis AJ. PMID: 23730305; PMCID: PMC3657633.
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PubMed Mentions:
10
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Mendel: the Swiss army knife of genetic analysis programs. Bioinformatics. 2013 Jun 15; 29(12):1568-70.
Lange K, Papp JC, Sinsheimer JS, Sripracha R, Zhou H, Sobel EM. PMID: 23610370; PMCID: PMC3673222.
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PubMed Mentions:
66 Fields:
Translation:
Humans
-
Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women. J Clin Endocrinol Metab. 2013 Mar; 98(3):E600-4.
Chan KH, Niu T, Ma Y, You NC, Song Y, Sobel EM, Hsu YH, Balasubramanian R, Qiao Y, Tinker L, Liu S. PMID: 23386649; PMCID: PMC3590470.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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Adult asthma and risk of coronary heart disease, cerebrovascular disease, and heart failure: a prospective study of 2 matched cohorts. Am J Epidemiol. 2012 Dec 01; 176(11):1014-24.
Iribarren C, Tolstykh IV, Miller MK, Sobel E, Eisner MD. PMID: 23139248.
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PubMed Mentions:
89 Fields:
Translation:
Humans
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Application of new method for evaluating performance of fracture risk tool. Am J Manag Care. 2012 10 01; 18(10):e398.
Sobel EM, Ettinger B, Lo JC, Pressman AR. PMID: 23145848.
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PubMed Mentions: Fields:
Translation:
Humans
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Mendel-GPU: haplotyping and genotype imputation on graphics processing units. Bioinformatics. 2012 Nov 15; 28(22):2979-80.
Chen GK, Wang K, Stram AH, Sobel EM, Lange K. PMID: 22954633; PMCID: PMC3634317.
View in:
PubMed Mentions:
6 Fields:
Translation:
Humans
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Quantitative trait Loci association mapping by imputation of strain origins in multifounder crosses. Genetics. 2012 Feb; 190(2):459-73.
Zhou JJ, Ghazalpour A, Sobel EM, Sinsheimer JS, Lange K. PMID: 22143921; PMCID: PMC3276647.
View in:
PubMed Mentions:
7 Fields:
Translation:
AnimalsCells
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Detection of intergenerational genetic effects with application to HLA-B matching as a risk factor for schizophrenia. Hum Hered. 2011; 72(3):161-72.
Childs EJ, Sobel EM, Palmer CG, Sinsheimer JS. PMID: 22004985; PMCID: PMC3721948.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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Unifying ideas for non-parametric linkage analysis. Hum Hered. 2011; 71(4):267-80.
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. PMID: 21822022; PMCID: PMC7077094.
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PubMed Mentions: Fields:
Translation:
Humans
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Linkage analysis without defined pedigrees. Genet Epidemiol. 2011 Jul; 35(5):360-70.
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. PMID: 21465549; PMCID: PMC3290352.
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PubMed Mentions:
22 Fields:
Translation:
Humans
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Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex. PLoS One. 2010 Apr 21; 5(4):e10292.
Gao MC, Bellugi U, Dai L, Mills DL, Sobel EM, Lange K, Korenberg JR. PMID: 20422020; PMCID: PMC2858212.
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PubMed Mentions:
19 Fields:
Translation:
HumansCells
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Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC. Invest Ophthalmol Vis Sci. 2010 Aug; 51(8):4006-12.
Aldave AJ, Rosenwasser GO, Yellore VS, Papp JC, Sobel EM, Pham MN, Chen MC, Dandekar S, Sripracha R, Rayner SA, Sassani JW, Gorin MB. PMID: 20357198; PMCID: PMC2910638.
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PubMed Mentions:
4 Fields:
Translation:
HumansCells
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Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval. Cornea. 2009 Aug; 28(7):801-7.
Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel E, Papp J. PMID: 19574904; PMCID: PMC2714875.
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PubMed Mentions:
10 Fields:
Translation:
HumansCells
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The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies. Proc Natl Acad Sci U S A. 2009 Jul 21; 106(29):12031-6.
Korbel JO, Tirosh-Wagner T, Urban AE, Chen XN, Kasowski M, Dai L, Grubert F, Erdman C, Gao MC, Lange K, Sobel EM, Barlow GM, Aylsworth AS, Carpenter NJ, Clark RD, Cohen MY, Doran E, Falik-Zaccai T, Lewin SO, Lott IT, McGillivray BC, Moeschler JB, Pettenati MJ, Pueschel SM, Rao KW, Shaffer LG, Shohat M, Van Riper AJ, Warburton D, Weissman S, Gerstein MB, Snyder M, Korenberg JR. PMID: 19597142; PMCID: PMC2709665.
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PubMed Mentions:
183 Fields:
Translation:
HumansCells
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Genome-wide association analysis by lasso penalized logistic regression. Bioinformatics. 2009 Mar 15; 25(6):714-21.
Wu TT, Chen YF, Hastie T, Sobel E, Lange K. PMID: 19176549; PMCID: PMC2732298.
View in:
PubMed Mentions:
312 Fields:
-
Integrated weighted gene co-expression network analysis with an application to chronic fatigue syndrome. BMC Syst Biol. 2008 Nov 06; 2:95.
Presson AP, Sobel EM, Papp JC, Suarez CJ, Whistler T, Rajeevan MS, Vernon SD, Horvath S. PMID: 18986552; PMCID: PMC2625353.
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PubMed Mentions:
96 Fields:
Translation:
Humans
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Mixed effects models for quantitative trait loci mapping with inbred strains. Genetics. 2008 Nov; 180(3):1743-61.
Bauman LE, Sinsheimer JS, Sobel EM, Lange K. PMID: 18791243; PMCID: PMC2581972.
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PubMed Mentions:
5 Fields:
Translation:
Animals
-
WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. Am J Hum Genet. 2008 Aug; 83(2):180-92.
Lee JC, Weissglas-Volkov D, Kyttälä M, Dastani Z, Cantor RM, Sobel EM, Plaisier CL, Engert JC, van Greevenbroek MM, Kane JP, Malloy MJ, Pullinger CR, Huertas-Vazquez A, Aguilar-Salinas CA, Tusie-Luna T, de Bruin TW, Aouizerat BE, van der Kallen CC, Croce CM, Aqeilan RI, Marcil M, Viikari JS, Lehtimäki T, Raitakari OT, Kuusisto J, Laakso M, Taskinen MR, Genest J, Pajukanta P. PMID: 18674750; PMCID: PMC2495060.
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PubMed Mentions:
34 Fields:
Translation:
Humans
-
Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis. BMC Bioinformatics. 2008 Jul 21; 9:317.
Presson AP, Sobel EM, Pajukanta P, Plaisier C, Weeks DE, Aberg K, Papp JC. PMID: 18644149; PMCID: PMC2515855.
View in:
PubMed Mentions:
2 Fields:
Translation:
Cells
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A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus). Mamm Genome. 2007 May; 18(5):347-60.
Jasinska AJ, Service S, Levinson M, Slaten E, Lee O, Sobel E, Fairbanks LA, Bailey JN, Jorgensen MJ, Breidenthal SE, Dewar K, Hudson TJ, Palmour R, Freimer NB, Ophoff RA. PMID: 17629771.
View in:
PubMed Mentions:
22 Fields:
Translation:
HumansAnimalsCells
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A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees. Genet Epidemiol. 2007 Jul; 31(5):417-30.
Brock GN, Weeks DE, Sobel E, Feingold E. PMID: 17508354.
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PubMed Mentions:
1 Fields:
Translation:
Humans
-
Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20. Genet Med. 2007 Apr; 9(4):228-34.
Yellore VS, Papp JC, Sobel E, Khan MA, Rayner SA, Farber DB, Aldave AJ. PMID: 17438387.
View in:
PubMed Mentions:
17 Fields:
Translation:
HumansCells
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Confirmation of psoriasis susceptibility loci on chromosome 6p21 and 20p13 in French families. J Invest Dermatol. 2007 Jun; 127(6):1403-9.
Lesueur F, Lefèvre C, Has C, Guilloud-Bataille M, Oudot T, Mahé E, Lahfa M, Mansouri S, Mosharraf-Olmolk H, Sobel E, Heath S, Lathrop M, Dizier MH, Prud'Homme JF, Fischer J. PMID: 17344932.
View in:
PubMed Mentions:
9 Fields:
Translation:
HumansCells
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Merging microsatellite data. J Comput Biol. 2006 Jul-Aug; 13(6):1131-47.
Presson AP, Sobel E, Lange K, Papp JC. PMID: 16901233.
View in:
PubMed Mentions:
7 Fields:
Translation:
Cells
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Variance component models for X-linked QTLs. Genet Epidemiol. 2006 Jul; 30(5):380-3.
Lange K, Sobel E. PMID: 16671110.
View in:
PubMed Mentions:
5 Fields:
Translation:
Humans
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Fine mapping of the multiple sclerosis susceptibility locus on 5p14-p12. J Neuroimmunol. 2005 Dec 30; 170(1-2):122-33.
Riise Stensland HM, Saarela J, Bronnikov DO, Parkkonen M, Jokiaho AJ, Palotie A, Tienari PJ, Sumelahti ML, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Sobel E, Peltonen L. PMID: 16169605.
View in:
PubMed Mentions:
4 Fields:
Translation:
HumansCells
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Association testing with Mendel. Genet Epidemiol. 2005 Jul; 29(1):36-50.
Lange K, Sinsheimer JS, Sobel E. PMID: 15834862.
View in:
PubMed Mentions:
43 Fields:
Translation:
Humans
-
Diagnostic accuracy for lupus and other systemic autoimmune diseases in the community setting. Arch Intern Med. 2004 Dec 13-27; 164(22):2435-41.
Narain S, Richards HB, Satoh M, Sarmiento M, Davidson R, Shuster J, Sobel E, Hahn P, Reeves WH. PMID: 15596633.
View in:
PubMed Mentions:
29 Fields:
Translation:
Humans
-
Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia. J Lipid Res. 2004 Oct; 45(10):1876-84.
Lilja HE, Suviolahti E, Soro-Paavonen A, Hiekkalinna T, Day A, Lange K, Sobel E, Taskinen MR, Peltonen L, Perola M, Pajukanta P. PMID: 15258200.
View in:
PubMed Mentions:
8 Fields:
Translation:
HumansCells
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Efficient simulation of P values for linkage analysis. Genet Epidemiol. 2004 Feb; 26(2):88-96.
Song KK, Weeks DE, Sobel E, Feingold E. PMID: 14748008.
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PubMed Mentions:
6 Fields:
Translation:
Humans
-
Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24. Hum Mol Genet. 2002 Sep 15; 11(19):2257-67.
Saarela J, Schoenberg Fejzo M, Chen D, Finnilä S, Parkkonen M, Kuokkanen S, Sobel E, Tienari PJ, Sumelahti ML, Wikström J, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Palotie A, Peltonen L. PMID: 12217954.
View in:
PubMed Mentions:
9 Fields:
Translation:
HumansCells
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A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet. 2002 Mar; 70(3):652-62.
Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Färkkilä M, Peltonen L, Palotie A. PMID: 11836652; PMCID: PMC384944.
View in:
PubMed Mentions:
46 Fields:
Translation:
HumansCells
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Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet. 2002 Feb; 70(2):496-508.
Sobel E, Papp JC, Lange K. PMID: 11791215; PMCID: PMC384922.
View in:
PubMed Mentions:
140 Fields:
Translation:
Humans