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Eric Lynch

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Sarah B Pierce; Karen M Chisholm; Eric D Lynch; Ming K Lee; Tom Walsh; John M Opitz; Weiqing Li; Rachel E Klevit; Mary-Claire King
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.
Hashem Shahin; Tom Walsh; Tama Sobe; Judeh Abu Sa'ed; Amal Abu Rayan; Eric D Lynch; Ming K Lee; Karen B Avraham; Mary-Claire King; Moien Kanaan
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.
Leonard Lipovich; Eric D Lynch; Ming K Lee; Mary-Claire King
A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31.

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All Publications

2011: Sarah B Pierce; Karen M Chisholm; Eric D Lynch; Ming K Lee; Tom Walsh; John M Opitz; Weiqing Li; Rachel E Klevit; Mary-Claire King
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.
Proceedings of the National Academy of Sciences of the United States of America 2011;108(16):6543-8.
2006: Hashem Shahin; Tom Walsh; Tama Sobe; Judeh Abu Sa'ed; Amal Abu Rayan; Eric D Lynch; Ming K Lee; Karen B Avraham; Mary-Claire King; Moien Kanaan
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.
American journal of human genetics 2006;78(1):144-52.
2001: Leonard Lipovich; Eric D Lynch; Ming K Lee; Mary-Claire King
A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31.
Genome biology 2001;2(4):RESEARCH0011.
2000: John Quigley; Cara Carthel Burns; Maria M Anderson; Eric D Lynch; Kathleen M Sabo; Julie Overbaugh; Janis L Abkowitz
Cloning of the cellular receptor for feline leukemia virus subgroup C (FeLV-C), a retrovirus that induces red cell aplasia.
Blood 2000;95(3):1093-9.
2000: Eric D Lynch; P E León
Non-syndromic dominant DFNA1.
Advances in oto-rhino-laryngology 2000;56():60-7.
1998: Anil K Lalwani; Robert K Jackler; Robert W Sweetow; Eric D Lynch; H Raventós; J Morrow; Mary-Claire King; P E León
Further characterization of the DFNA1 audiovestibular phenotype.
Archives of otolaryngology--head & neck surgery 1998;124(6):699-702.
1998: O Vahava; R Morell; Eric D Lynch; Sigal Weiss; M E Kagan; Nadav Ahituv; JE Morrow; Ming K Lee; AB Skvorak; Cynthia C Morton; A Blumenfeld; Moshe Frydman; Thomas B Friedman; Mary-Claire King; Karen B Avraham
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.
Science (New York, N.Y.) 1998;279(5358):1950-4.
1998: M K Lee; Eric D Lynch; Mary-Claire King
SeqHelp: a program to analyze molecular sequences utilizing common computational resources.
Genome research 1998;8(3):306-12.
1997: AB Skvorak; Nahid G Robertson; Y Yin; Stanislawa Weremowicz; H Her; Frederick R Bieber; K W Beisel; Eric D Lynch; David Beier; Cynthia C Morton
An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1).
Genomics 1997;46(2):191-9.
1997: Eric D Lynch; E A Ostermeyer; Ming K Lee; J F Arena; H Ji; JL Dann; Karen Swisshelm; D Suchard; P M MacLeod; S Kvinnsland; Bjorn T Gjertsen; K Heimdal; Herbert A Lubs; P Møller; Mary-Claire King
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.
American journal of human genetics 1997;61(6):1254-60.
1997: Eric D Lynch; Ming K Lee; JE Morrow; Piri Welcsh; P E León; Mary-Claire King
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
Science (New York, N.Y.) 1997;278(5341):1315-8.
1996: K J Abel; Lawrence C Brody; J M Valdes; Michael R Erdos; D R McKinley; Lucio H Castilla; Sofia D Merajver; Fergus J. Couch; L S Friedman; E A Ostermeyer; Eric D Lynch; Mary-Claire King; Piri Welcsh; S Osborne-Lawrence; M Spillman; Anne M Bowcock; Francis S Collins; Barbara L Weber
Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1.
Genomics 1996;37(2):161-71.
1995: L S Friedman; E A Ostermeyer; Eric D Lynch; Piri Welcsh; C I Szabo; J E Meza; L A Anderson; P Dowd; Ming K Lee; S E Rowell
22 genes from chromosome 17q21: cloning, sequencing, and characterization of mutations in breast cancer families and tumors.
Genomics 1995;25(1):256-63.
1994: L S Friedman; E A Ostermeyer; Eric D Lynch; C I Szabo; L A Anderson; P Dowd; Ming K Lee; S E Rowell; J Boyd; Mary-Claire King
The search for BRCA1.
Cancer research 1994;54(24):6374-82.
1994: L S Friedman; E A Ostermeyer; C I Szabo; P Dowd; Eric D Lynch; S E Rowell; Mary-Claire King
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families.
Nature genetics 1994;8(4):399-404.
1994: E A Ostermeyer; L S Friedman; Eric D Lynch; C I Szabo; P Dowd; Ming K Lee; S E Rowell; Mary-Claire King
Green pigs, red herrings, and a golden hoe: a retrospective on the identification of BRCA1 and the beginning of its characterization.
Cold Spring Harbor symposia on quantitative biology 1994;59():523-30.
1993: W L Flejter; C L Barcroft; S W Guo; Eric D Lynch; Michael Boehnke; Settara C Chandrasekharappa; S Hayes; Francis S Collins; Barbara L Weber; Thomas W Glover
Multicolor FISH mapping with Alu-PCR-amplified YAC clone DNA determines the order of markers in the BRCA1 region on chromosome 17q12-q21.
Genomics 1993;17(3):624-31.
1993: RV Lebo; Eric D Lynch; M S Golbus; R R Flandermeyer; Pauline H Yen; Lawrence J Shapiro
Prenatal in situ hybridization test for deleted steroid sulfatase gene.
American journal of medical genetics 1993;46(6):652-8.
1993: L S Friedman; Eric D Lynch; Mary-Claire King
Two independent polymorphisms at the 17 beta-hydroxysteroid dehydrogenase (EDH17B) gene (17q21).
Human molecular genetics 1993;2(6):821.
1992: RV Lebo; R R Flandermeyer; R Diukman; Eric D Lynch; J A Lepercq; M S Golbus
Prenatal diagnosis with repetitive in situ hybridization probes.
American journal of medical genetics 1992;43(5):848-54.
1992: Jeannette Bonifas; J W Bare; Eric D Lynch; RV Lebo; Ervin H Epstein
Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization.
Genomics 1992;13(2):452-4.
1992: RV Lebo; Eric D Lynch; Thomas D Bird; M S Golbus; David Barker; P O'Connell; P F Chance
Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers.
American journal of human genetics 1992;50(1):42-55.
1991: RV Lebo; Eric D Lynch; J Wiegant; K Moore; M Trounstine; M van der Ploeg
Multicolor fluorescence in situ hybridization and pulsed field electrophoresis dissect CMT1B gene region.
Human genetics 1991;88(1):13-20.
1991: RV Lebo; P F Chance; P J Dyck; M T Redila-Flores; Eric D Lynch; M S Golbus; Thomas D Bird; Mary-Claire King; L A Anderson; J Hall
Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.
Human genetics 1991;88(1):1-12.