Christina Palmer

Title(s)Professor-in-Residence, Psychiatry and Biobehavioral Sciences
SchoolMedicine
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    Collapse Research 
    Collapse Research Activities and Funding
    UCLA clinical site for the investigation of undiagnosed disorders
    NIH U01HG007703Jul 1, 2014 - Jun 30, 2022
    Role: Co-Principal Investigator
    Cancer Genetics Education for the Deaf Community
    NIH R25CA154290Aug 4, 2011 - Jul 31, 2016
    Role: Principal Investigator
    Outcomes of Cx26 Testing in Deaf/Hard of Hearing Adults
    NIH R01HG003871Sep 1, 2006 - Aug 31, 2011
    Role: Principal Investigator
    Connexin 26 Testing in Infants
    NIH R01DC005663Sep 23, 2002 - Aug 31, 2007
    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. Genetic counseling delivery, outcomes, training, and practice in response to COVID-19: Introduction to the special issue. J Genet Couns. 2021 Aug; 30(4):922-923. Cohen SA, Myers M, Palmer CGS, Trepanier A. PMID: 34378274; PMCID: PMC8427082.
      View in: PubMed   Mentions: 1     Fields:    
    2. Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples. J Genet Couns. 2022 02; 31(1):59-70. McConkie-Rosell A, Schoch K, Sullivan J, Spillmann RC, Cope H, Tan QK, Palmer CGS, Undiagnosed Disease Network, Hooper SR, Shashi V. PMID: 34115423; PMCID: PMC8664895.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    3. Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain. Genet Med. 2021 08; 23(8):1465-1473. Marbach F, Stoyanov G, Erger F, Stratakis CA, Settas N, London E, Rosenfeld JA, Torti E, Haldeman-Englert C, Sklirou E, Kessler E, Ceulemans S, Nelson SF, Martinez-Agosto JA, Palmer CGS, Signer RH, Undiagnosed Diseases Network, Andrews MV, Grange DK, Willaert R, Person R, Telegrafi A, Sievers A, Laugsch M, Theiß S, Cheng Y, Lichtarge O, Katsonis P, Stocco A, Schaaf CP. PMID: 33833410; PMCID: PMC8354857.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    4. Expansion of NEUROD2 phenotypes to include developmental delay without seizures. Am J Med Genet A. 2021 04; 185(4):1076-1080. Mis EK, Sega AG, Signer RH, Cartwright T, Ji W, Martinez-Agosto JA, Nelson SF, Palmer CGS, Lee H, Mitzelfelt T, Konstantino M, Undiagnosed Diseases Network, Jeffries L, Khokha MK, Marco E, Martin MG, Lakhani SA. PMID: 33438828; PMCID: PMC8212414.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    5. Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients. Sci Adv. 2020 12; 6(49). Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG, DDD Study, Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, Õunap K, Ilves P, Innes AM, Kernohan KD, Care4Rare Canada Consortium, Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H, CAUSES Study, Martin MG, Martinez-Agosto JA, Undiagnosed Diseases Network, Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vøllo A, Prescott T, Fagerberg C, Laulund LW, Larsen MJ, Byler M, Lebel RR, Hurst AC, Dean J, Schrier Vergano SA, Norman J, Mercimek-Andrews S, Neira J, Van Allen MI, Longo N, Sellars E, Louie RJ, Cathey SS, Brokamp E, Heron D, Snyder M, Vanderver A, Simon C, de la Cruz X, Padilla N, Crump JG, Chung W, Garcia B, Hakonarson HH, Bhoj EJ. PMID: 33268356; PMCID: PMC7821880.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansAnimals
    6. Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice. J Genet Couns. 2021 04; 30(2):439-447. Studwell CM, Kelley EG, Undiagnosed Diseases Network, Sinsheimer JS, Palmer CGS, LeBlanc K. PMID: 33108040; PMCID: PMC8207526.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    7. Novel NUDT2 variant causes intellectual disability and polyneuropathy. Ann Clin Transl Neurol. 2020 11; 7(11):2320-2325. Diaz F, Khosa S, Niyazov D, Lee H, Person R, Morrow MM, Signer R, Dorrani N, Zheng A, Herzog M, Freundlich R, Undiagnosed Diseases Network, Birath JB, Cervantes-Manzo Y, Martinez-Agosto JA, Palmer C, Nelson SF, Fogel BL, Mishra SK. PMID: 33058507; PMCID: PMC7664258.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    8. Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencing. Neuropathology. 2020 Jun; 40(3):302-307. Woods JD, Khanlou N, Lee H, Signer R, Shieh P, Chen J, Herzog M, Palmer C, Martinez-Agosto J, Undiagnosed Diseases Network, Nelson SF. PMID: 32037607; PMCID: PMC7317439.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    9. Alternative option labeling impacts decision-making in noninvasive prenatal screening. J Genet Couns. 2020 12; 29(6):910-918. Fisher CF, Birkeland LE, Reiser CA, Zhao Q, Palmer CGS, Zikmund-Fisher BJ, Petty EM. PMID: 31793699.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genet Med. 2020 03; 22(3):490-499. Lee H, Huang AY, Wang LK, Yoon AJ, Renteria G, Eskin A, Signer RH, Dorrani N, Nieves-Rodriguez S, Wan J, Douine ED, Woods JD, Dell'Angelica EC, Fogel BL, Martin MG, Butte MJ, Parker NH, Wang RT, Shieh PB, Wong DA, Gallant N, Singh KE, Tavyev Asher YJ, Sinsheimer JS, Krakow D, Loo SK, Allard P, Papp JC, Undiagnosed Diseases Network, Palmer CGS, Martinez-Agosto JA, Nelson SF. PMID: 31607746; PMCID: PMC7405636.
      View in: PubMed   Mentions: 84     Fields:    Translation:HumansCells
    11. The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease. Clin Genet. 2019 12; 96(6):521-531. McConkie-Rosell A, Schoch K, Sullivan J, Cope H, Spillmann R, Palmer CGS, Pena L, Jiang YH, Daniels N, Walley N, Tan KG, Undiagnosed Diseases Network, Hooper SR, Shashi V. PMID: 31448412; PMCID: PMC6983919.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    12. Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing. J Genet Couns. 2019 12; 28(6):1107-1118. Reuter CM, Kohler JN, Bonner D, Zastrow D, Fernandez L, Dries A, Marwaha S, Davidson J, Brokamp E, Herzog M, Hong J, Macnamara E, Rosenfeld JA, Schoch K, Spillmann R, Undiagnosed Diseases Network, Loscalzo J, Krier J, Stoler J, Sweetser D, Palmer CGS, Phillips JA, Shashi V, Adams DA, Yang Y, Ashley EA, Fisher PG, Mulvihill JJ, Bernstein JA, Wheeler MT. PMID: 31478310; PMCID: PMC6901723.
      View in: PubMed   Mentions: 24     Fields:    Translation:Humans
    13. SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals. Hum Mutat. 2019 07; 40(7):908-925. Ng BG, Sosicka P, Agadi S, Almannai M, Bacino CA, Barone R, Botto LD, Burton JE, Carlston C, Chung BH, Cohen JS, Coman D, Dipple KM, Dorrani N, Dobyns WB, Elias AF, Epstein L, Gahl WA, Garozzo D, Hammer TB, Haven J, Héron D, Herzog M, Hoganson GE, Hunter JM, Jain M, Juusola J, Lakhani S, Lee H, Lee J, Lewis K, Longo N, Lourenço CM, Mak CCY, McKnight D, Mendelsohn BA, Mignot C, Mirzaa G, Mitchell W, Muhle H, Nelson SF, Olczak M, Palmer CGS, Partikian A, Patterson MC, Pierson TM, Quinonez SC, Regan BM, Ross ME, Guillen Sacoto MJ, Scaglia F, Scheffer IE, Segal D, Singhal NS, Striano P, Sturiale L, Symonds JD, Tang S, Vilain E, Willis M, Wolfe LA, Yang H, Yano S, Powis Z, Suchy SF, Rosenfeld JA, Edmondson AC, Grunewald S, Freeze HH. PMID: 30817854; PMCID: PMC6661012.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansAnimalsCells
    14. Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era. J Genet Couns. 2019 04; 28(2):194-201. Macnamara EF, Schoch K, Kelley EG, Fieg E, Brokamp E, Undiagnosed Diseases Network, Signer R, LeBlanc K, McConkie-Rosell A, Palmer CGS. PMID: 30680851; PMCID: PMC6456366.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    15. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. N Engl J Med. 2018 11 29; 379(22):2131-2139. Splinter K, Adams DR, Bacino CA, Bellen HJ, Bernstein JA, Cheatle-Jarvela AM, Eng CM, Esteves C, Gahl WA, Hamid R, Jacob HJ, Kikani B, Koeller DM, Kohane IS, Lee BH, Loscalzo J, Luo X, McCray AT, Metz TO, Mulvihill JJ, Nelson SF, Palmer CGS, Phillips JA, Pick L, Postlethwait JH, Reuter C, Shashi V, Sweetser DA, Tifft CJ, Walley NM, Wangler MF, Westerfield M, Wheeler MT, Wise AL, Worthey EA, Yamamoto S, Ashley EA, Undiagnosed Diseases Network. PMID: 30304647; PMCID: PMC6481166.
      View in: PubMed   Mentions: 143     Fields:    Translation:HumansAnimals
    16. Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network. J Genet Couns. 2018 09; 27(5):1087-1101. Palmer CGS, McConkie-Rosell A, Holm IA, LeBlanc K, Sinsheimer JS, Briere LC, Dorrani N, Herzog MR, Lincoln S, Schoch K, Spillmann RC, Brokamp E, Undiagnosed Diseases Network. PMID: 29497923; PMCID: PMC6132569.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    17. Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? J Genet Couns. 2018 08; 27(4):935-946. McConkie-Rosell A, Hooper SR, Pena LDM, Schoch K, Spillmann RC, Jiang YH, Cope H, Undiagnosed Diseases Network, Palmer C, Shashi V. PMID: 29297108; PMCID: PMC6028305.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    18. Bilingual Cancer Genetic Education Modules for the Deaf Community: Development and Evaluation of the Online Video Material. J Genet Couns. 2018 04; 27(2):457-469. Boudreault P, Wolfson A, Berman B, Venne VL, Sinsheimer JS, Palmer C. PMID: 29260487; PMCID: PMC5860968.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    19. Bilingual approach to online cancer genetics education for Deaf American Sign Language users produces greater knowledge and confidence than English text only: A randomized study. Disabil Health J. 2017 01; 10(1):23-32. Palmer CG, Boudreault P, Berman BA, Wolfson A, Duarte L, Venne VL, Sinsheimer JS. PMID: 27594054; PMCID: PMC5136526.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    20. 2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling. J Genet Couns. 2016 10; 25(5):868-79. Doyle DL, Awwad RI, Austin JC, Baty BJ, Bergner AL, Brewster SJ, Erby LA, Franklin CR, Greb AE, Grubs RE, Hooker GW, Noblin SJ, Ormond KE, Palmer CG, Petty EM, Singletary CN, Thomas MJ, Toriello H, Walton CS, Uhlmann WR. PMID: 27333894.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    21. Clinical exome sequencing for genetic identification of rare Mendelian disorders. JAMA. 2014 Nov 12; 312(18):1880-7. Lee H, Deignan JL, Dorrani N, Strom SP, Kantarci S, Quintero-Rivera F, Das K, Toy T, Harry B, Yourshaw M, Fox M, Fogel BL, Martinez-Agosto JA, Wong DA, Chang VY, Shieh PB, Palmer CG, Dipple KM, Grody WW, Vilain E, Nelson SF. PMID: 25326637; PMCID: PMC4278636.
      View in: PubMed   Mentions: 465     Fields:    Translation:Humans
    22. Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudinal study. PLoS One. 2014; 9(11):e111512. Palmer CG, Boudreault P, Baldwin EE, Sinsheimer JS. PMID: 25375116; PMCID: PMC4222828.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    23. Assessing deaf awareness training: knowledge and attitudes of recent genetic counseling graduates. J Genet Couns. 2015 Feb; 24(1):104-16. Nagakura H, Schneider G, Morris J, Lafferty KA, Palmer CG. PMID: 25030269.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    24. Evidence synthesis and guideline development in genomic medicine: current status and future prospects. Genet Med. 2015 Jan; 17(1):63-7. Schully SD, Lam TK, Dotson WD, Chang CQ, Aronson N, Birkeland ML, Brewster SJ, Boccia S, Buchanan AH, Calonge N, Calzone K, Djulbegovic B, Goddard KA, Klein RD, Klein TE, Lau J, Long R, Lyman GH, Morgan RL, Palmer CG, Relling MV, Rubinstein WS, Swen JJ, Terry SF, Williams MS, Khoury MJ. PMID: 24946156; PMCID: PMC4272332.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    25. Next generation genetic counseling: introduction to the special issue. J Genet Couns. 2014 Aug; 23(4):439-44. Roche MI, Palmer CG. PMID: 24838698; PMCID: PMC4096054.
      View in: PubMed   Mentions: 2     Fields:    
    26. American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Genet Med. 2014 Apr; 16(4):347-55. Alford RL, Arnos KS, Fox M, Lin JW, Palmer CG, Pandya A, Rehm HL, Robin NH, Scott DA, Yoshinaga-Itano C, ACMG Working Group on Update of Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congen, Professional Practice and Guidelines Committee. PMID: 24651602.
      View in: PubMed   Mentions: 82     Fields:    Translation:Humans
    27. Using a social marketing framework to evaluate recruitment of a prospective study of genetic counseling and testing for the deaf community. BMC Med Res Methodol. 2013 Nov 25; 13:145. Kobayashi Y, Boudreault P, Hill K, Sinsheimer JS, Palmer CG. PMID: 24274380; PMCID: PMC3924226.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    28. Deaf genetic testing and psychological well-being in deaf adults. J Genet Couns. 2013 Aug; 22(4):492-507. Palmer CG, Boudreault P, Baldwin EE, Fox M, Deignan JL, Kobayashi Y, Sininger Y, Grody W, Sinsheimer JS. PMID: 23430402; PMCID: PMC3701749.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    29. 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.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    30. Effect of pre-test genetic counseling for deaf adults on knowledge of genetic testing. J Genet Couns. 2012 Apr; 21(2):256-72. Baldwin EE, Boudreault P, Fox M, Sinsheimer JS, Palmer CG. PMID: 21818696; PMCID: PMC3313024.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    31. Modeling maternal-offspring gene-gene interactions: the extended-MFG test. Genet Epidemiol. 2010 Jul; 34(5):512-21. Childs EJ, Palmer CG, Lange K, Sinsheimer JS. PMID: 20552637; PMCID: PMC3165170.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    32. Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study. J Deaf Stud Deaf Educ. 2010; 15(3):209-27. Boudreault P, Baldwin EE, Fox M, Dutton L, Tullis L, Linden J, Kobayashi Y, Zhou J, Sinsheimer JS, Sininger Y, Grody WW, Palmer CG. PMID: 20488870; PMCID: PMC2902357.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    33. Evidence for maternal-fetal genotype incompatibility as a risk factor for schizophrenia. J Biomed Biotechnol. 2010; 2010:576318. Palmer CG. PMID: 20379378; PMCID: PMC2850511.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    34. Publishing a master's thesis: a guide for novice authors. J Genet Couns. 2010 Jun; 19(3):217-27. Resta RG, McCarthy Veach P, Charles S, Vogel K, Blase T, Palmer CG. PMID: 20076994; PMCID: PMC2874663.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    35. Examining the relationship between genetic counselors' attitudes toward deaf people and the genetic counseling session. J Genet Couns. 2010 Apr; 19(2):161-73. Enns EE, Boudreault P, Palmer CG. PMID: 19904587; PMCID: PMC2832890.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    36. A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants. Am J Med Genet A. 2009 Jun; 149A(6):1169-82. Palmer CG, Martinez A, Fox M, Zhou J, Shapiro N, Sininger Y, Grody WW, Schimmenti LA. PMID: 19449415; PMCID: PMC2866144.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    37. Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child. Genet Med. 2009 Apr; 11(4):248-55. Palmer CG, Lueddeke JT, Zhou J. PMID: 19265722; PMCID: PMC2822638.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    38. Effect of Rhesus D incompatibility on schizophrenia depends on offspring sex. Schizophr Res. 2008 Sep; 104(1-3):135-45. Palmer CG, Mallery E, Turunen JA, Hsieh HJ, Peltonen L, Lonnqvist J, Woodward JA, Sinsheimer JS. PMID: 18692992; PMCID: PMC2572267.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    39. Infant hearing loss and connexin testing in a diverse population. Genet Med. 2008 Jul; 10(7):517-24. Schimmenti LA, Martinez A, Telatar M, Lai CH, Shapiro N, Fox M, Warman B, McCarra M, Crandall B, Sininger Y, Grody WW, Palmer CG. PMID: 18580690.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    40. Using the maternal-fetal genotype incompatibility test to assess non-inherited maternal HLA-DRB1 antigen coding alleles as rheumatoid arthritis risk factors. BMC Proc. 2007; 1 Suppl 1:S124. Hsieh HJ, Palmer CG, Harney S, Chen HW, Bauman L, Brown MA, Sinsheimer JS. PMID: 18466466; PMCID: PMC2367472.
      View in: PubMed   Mentions: 2  
    41. Psychiatric disorders in clinical genetics II: Individualizing recurrence risks. J Genet Couns. 2008 Feb; 17(1):18-29. Austin JC, Palmer CG, Rosen-Sheidley B, Veach PM, Gettig E, Peay HL. PMID: 18071888.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    42. Psychiatric disorders in clinical genetics I: Addressing family histories of psychiatric illness. J Genet Couns. 2008 Feb; 17(1):6-17. Peay HL, Veach PM, Palmer CG, Rosen-Sheidley B, Gettig E, Austin JC. PMID: 17963028.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    43. Ethnic differences in parental perceptions of genetic testing for deaf infants. J Genet Couns. 2008 Feb; 17(1):129-38. Palmer CG, Martinez A, Fox M, Sininger Y, Grody WW, Schimmenti LA. PMID: 17952575.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    44. Sharing GJB2/GJB6 genetic test information with family members. J Genet Couns. 2007 Jun; 16(3):313-24. Blase T, Martinez A, Grody WW, Schimmenti L, Palmer CG. PMID: 17318457.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    45. Allowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects. Hum Hered. 2006; 62(3):165-74. Hsieh HJ, Palmer CG, Sinsheimer JS. PMID: 17065817.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    46. HLA-B maternal-fetal genotype matching increases risk of schizophrenia. Am J Hum Genet. 2006 Oct; 79(4):710-5. Palmer CG, Hsieh HJ, Reed EF, Lonnqvist J, Peltonen L, Woodward JA, Sinsheimer JS. PMID: 16960807; PMCID: PMC1592576.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    47. The v-MFG test: investigating maternal, offspring and maternal-fetal genetic incompatibility effects on disease and viability. Genet Epidemiol. 2006 May; 30(4):333-47. Hsieh HJ, Palmer CG, Harney S, Newton JL, Wordsworth P, Brown MA, Sinsheimer JS. PMID: 16607625.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    48. Prelingual siblings of children with GJB2 hearing loss: issues to consider. Arch Otolaryngol Head Neck Surg. 2005 Nov; 131(11):1020-2. Palmer CG, Martinez A, Sininger Y, Shapiro N, Grody WW, Schimmenti LA. PMID: 16301377.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    49. Evaluating the impact of genetic counseling and testing with signal detection methods. J Genet Couns. 2005 Feb; 14(1):17-27. Palmer CG, Hadley DW. PMID: 15789153.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    50. An exact maternal-fetal genotype incompatibility (MFG) test. Genet Epidemiol. 2005 Jan; 28(1):83-95. Minassian SL, Palmer CG, Sinsheimer JS. PMID: 15368616.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    51. Genetic testing as part of the early hearing detection and intervention (EHDI) process. Genet Med. 2004 Nov-Dec; 6(6):521-5. Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Palmer CG. PMID: 15545749.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansPHPublic Health
    52. RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order. Eur J Hum Genet. 2004 Mar; 12(3):192-8. Kraft P, Palmer CG, Woodward AJ, Turunen JA, Minassian S, Paunio T, Lönnqvist J, Peltonen L, Sinsheimer JS. PMID: 14735156.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    53. Colon cancer screening practices after genetic counseling and testing for hereditary nonpolyposis colorectal cancer. J Clin Oncol. 2004 Jan 01; 22(1):39-44. Hadley DW, Jenkins JF, Dimond E, de Carvalho M, Kirsch I, Palmer CG. PMID: 14701766.
      View in: PubMed   Mentions: 62     Fields:    Translation:HumansPHPublic Health
    54. Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness. Genet Med. 2003 Mar-Apr; 5(2):106-12. Martinez A, Linden J, Schimmenti LA, Palmer CG. PMID: 12644780.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    55. Detecting genotype combinations that increase risk for disease: maternal-fetal genotype incompatibility test. Genet Epidemiol. 2003 Jan; 24(1):1-13. Sinsheimer JS, Palmer CG, Woodward JA. PMID: 12508251.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    56. Genetic linkage and association between chromosome 1q and working memory function in schizophrenia. Am J Med Genet B Neuropsychiatr Genet. 2003 Jan 01; 116B(1):8-16. Gasperoni TL, Ekelund J, Huttunen M, Palmer CG, Tuulio-Henriksson A, Lönnqvist J, Kaprio J, Peltonen L, Cannon TD. PMID: 12497606.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
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