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Exploring perceptions of genetic counseling student-run free clinics as an innovative service delivery model to increase access to genetic counseling services. J Genet Couns. 2024 Sep 24.
Morgan S, Lajonchere C, Prelip M, Palmer CGS. PMID: 39318130.
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PubMed Mentions: Fields:
-
Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genet Med. 2024 Nov; 26(11):101218.
Huang Y, Jay KL, Yen-Wen Huang A, Wan J, Jangam SV, Chorin O, Rothschild A, Barel O, Mariani M, Iascone M, Xue H, Undiagnosed Diseases Network, Huang J, Mignot C, Keren B, Saillour V, Mah-Som AY, Sacharow S, Rajabi F, Costin C, Yamamoto S, Kanca O, Bellen HJ, Rosenfeld JA, Palmer CGS, Nelson SF, Wangler MF, Martinez-Agosto JA. PMID: 39036895; PMCID: PMC11648989.
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PubMed Mentions:
1 Fields:
Translation:
HumansAnimals
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Cultural, demographic, and other non-demographic factors associated with cancer genetic counseling patients' appointment accompaniment preferences in the United States. J Genet Couns. 2024 Jul 02.
Lin J, Cantor RM, Niell-Swiller M, Sayegh P, Palmer CGS. PMID: 38956816.
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PubMed Mentions: Fields:
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Exploring the role of digital tools in rare disease management: An interview-based study. J Genet Couns. 2024 May 13.
Chang A, Huang SD, Benjamin DJ, Schmidt JL, Palmer CGS, Garrison NA. PMID: 38741243.
View in:
PubMed Mentions:
1 Fields:
-
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.
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PubMed Mentions:
1 Fields:
-
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
-
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.
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PubMed Mentions:
7 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
4 Fields:
Translation:
HumansAnimals
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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.
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PubMed Mentions:
29 Fields:
Translation:
HumansAnimals
-
Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice. J Genet Couns. 2021 04; 30(2):439-447.
Studwell CM, Glanton E, Undiagnosed Diseases Network, Sinsheimer JS, Palmer CGS, LeBlanc K. PMID: 33108040; PMCID: PMC8207526.
View in:
PubMed Mentions:
2 Fields:
Translation:
Humans
-
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:
4 Fields:
Translation:
Humans
-
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
-
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.
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PubMed Mentions:
1 Fields:
Translation:
Humans
-
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:
93 Fields:
Translation:
HumansCells
-
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.
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PubMed Mentions:
2 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
25 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
29 Fields:
Translation:
HumansAnimalsCells
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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, Glanton E, Fieg E, Brokamp E, Undiagnosed Diseases Network, Signer R, LeBlanc K, McConkie-Rosell A, Palmer CGS. PMID: 30680851; PMCID: PMC6456366.
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PubMed Mentions:
12 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
173 Fields:
Translation:
HumansAnimals
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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.
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PubMed Mentions:
9 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
27 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
5 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
12 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
31 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
478 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
3 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
6 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
8 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
2 Fields:
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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.
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PubMed Mentions:
89 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
7 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
3 Fields:
Translation:
Humans
-
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:
4 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
11 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
5 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
18 Fields:
Translation:
Humans
-
Evidence for maternal-fetal genotype incompatibility as a risk factor for schizophrenia. J Biomed Biotechnol. 2010; 2010:576318.
Palmer CG. PMID: 20379378; PMCID: PMC2850511.
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PubMed Mentions:
6 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
2 Fields:
Translation:
Humans
-
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.
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PubMed Mentions:
10 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
13 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
13 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
7 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
14 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
2
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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.
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PubMed Mentions:
16 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
8 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
12 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
6 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
20 Fields:
Translation:
Humans
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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.
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PubMed Mentions:
11 Fields:
Translation:
Humans
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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.
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PubMed Mentions: Fields:
Translation:
Humans
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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.
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PubMed Mentions:
4 Fields:
Translation:
Humans
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An exact maternal-fetal genotype incompatibility (MFG) test. Genet Epidemiol. 2005 Jan; 28(1):83-95.
Minassian SL, Palmer CG, Sinsheimer JS. PMID: 15368616.
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PubMed Mentions:
2 Fields:
Translation:
Humans
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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
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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:
8 Fields:
Translation:
Humans
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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:
60 Fields:
Translation:
HumansPHPublic Health
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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
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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:
38 Fields:
Translation:
Humans
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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.
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RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility. Am J Hum Genet. 2002 Dec; 71(6):1312-9.
Palmer CG, Turunen JA, Sinsheimer JS, Minassian S, Paunio T, Lönnqvist J, Peltonen L, Woodward JA. PMID: 12439825; PMCID: PMC378569.
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A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. Am J Hum Genet. 2002 May; 70(5):1183-96.
Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. PMID: 11923911; PMCID: PMC447594.
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