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Lawrence Brody

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Karl C Desch; Joan E Bailey-Wilson; Lawrence C Brody; Andrew Crenshaw; Cheryl D Cropp; Yossi Kalish; Yoonhee Kim; Peadar N Kirke; Cathy C Laurie; Jun Z Li; Caitlin P McHugh; James L Mills; Daniel B Mirel; Anne M Molloy; Ayse B Ozel; John M Scott; Anjali A Sharathkumar; Jordan A Shavit; DR Siemieniak; Courtney D Thornburg; Alexander F Wilson; David Ginsburg
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Tonia C Carter; Mary R Conley; Charlotte M Druschel; Denise M Kay; Devon Kuehn; Aiyi Liu; Lawrence C Brody; Marilyn L Browne; Michele Caggana; Paul A Romitti; James L Mills
Anorectal atresia and variants at predicted regulatory sites in candidate genes.
Tonia C Carter; Mary R Conley; Charlotte M Druschel; Denise M Kay; Devon Kuehn; Aiyi Liu; Lawrence C Brody; Marilyn L Browne; Michele Caggana; Paul A Romitti; James L Mills
Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation.

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All Publications

2013: Karl C Desch; Joan E Bailey-Wilson; Lawrence C Brody; Andrew Crenshaw; Cheryl D Cropp; Yossi Kalish; Yoonhee Kim; Peadar N Kirke; Cathy C Laurie; Jun Z Li; Caitlin P McHugh; James L Mills; Daniel B Mirel; Anne M Molloy; Ayse B Ozel; John M Scott; Anjali A Sharathkumar; Jordan A Shavit; DR Siemieniak; Courtney D Thornburg; Alexander F Wilson; David Ginsburg
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Proceedings of the National Academy of Sciences of the United States of America 2013;110(2):588-93.
2013: Tonia C Carter; Mary R Conley; Charlotte M Druschel; Denise M Kay; Devon Kuehn; Aiyi Liu; Lawrence C Brody; Marilyn L Browne; Michele Caggana; Paul A Romitti; James L Mills
Anorectal atresia and variants at predicted regulatory sites in candidate genes.
Annals of human genetics 2013;77(1):31-46.
2012: Tonia C Carter; Mary R Conley; Charlotte M Druschel; Denise M Kay; Devon Kuehn; Aiyi Liu; Lawrence C Brody; Marilyn L Browne; Michele Caggana; Paul A Romitti; James L Mills
Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation.
Journal of human genetics 2012;57(8):485-93.
2012: Wayne A Cabral; David Chitayat; Kelly Cushing; Serigne M Gueye; Fizza Gulamali-Majid; Adebowale Adeyemo; Joan E Bailey-Wilson; Aileen M Barnes; Lawrence C Brody; SUSAN PANNY; Forbes D Porter; Timothy R Rebbeck; Charles N Rotimi; Sarah A Tishkoff; Joan C Marini
A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta.
Genetics in medicine : official journal of the American College of Medical Genetics 2012;14(5):543-51.
2012: James L Mills; Paul A Romitti; Denise M Kay; Aiyi Liu; Lawrence C Brody; Marilyn L Browne; Michele Caggana; Tonia C Carter; Charlotte M Druschel
Folate and vitamin B12-related genes and risk for omphalocele.
Human genetics 2012;131(5):739-46.
2012: Faith Pangilinan; Anne Parle-McDermott; Angelica Sanchez; John M Scott; Jessica M Seay; Barry Shane; Caroline Signore; Nicole Stone; James F Troendle; Julia E VanderMeer; Peter S Chines; Mary Conley; Joshua Cornman-Homonoff; Kerry Geiler-Samerotte; Peadar N Kirke; Kristine M Krebs; James L Mills; Adam Mitchell; Anne M Molloy; Valerie B O'Leary; Lawrence C Brody
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
BMC medical genetics 2012;13():62.
2012: Marina S Lee; R Reid Prentice; Erica L Sanchez; Eric T Sause; David J Bernard; Jenna R Bonner; Shawn M Burgess; Lawrence C Brody
Disruption of the folate pathway in zebrafish causes developmental defects.
BMC developmental biology 2012;12():12.
2012: Diana L Kolbe; Thomas C Krivak; Hanna M Petrykowska; Patricia Porter-Gill; Mary Strange; Lawrence C Brody; Julie A DeLoia; Alfred Guirguis; Laura Elnitski
Differential analysis of ovarian and endometrial cancers identifies a methylator phenotype.
PloS one 2012;7(3):e32941.
2011: James L Mills; Lawrence C Brody; Tonia C Carter; Eileen R Gibney; Peadar N Kirke; John M Scott; Barry Shane; James F Troendle; Per Magne Ueland; Anne M Molloy
Do high blood folate concentrations exacerbate metabolic abnormalities in people with low vitamin B-12 status?
The American journal of clinical nutrition 2011;94(2):495-500.
2011: Nicole Stone; Per Magne Ueland; Peadar N Kirke; James L Mills; Anne M Molloy; Faith Pangilinan; John M Scott; Praveen Sethupathy; Barry Shane; Lawrence C Brody
Bioinformatic and genetic association analysis of microRNA target sites in one-carbon metabolism genes.
PloS one 2011;6(7):e21851.
2011: Tonia C Carter; Faith Pangilinan; James F Troendle; Anne M Molloy; Julia VanderMeer; Adam Mitchell; Peadar N Kirke; Mary R Conley; Barry Shane; John M Scott; Lawrence C Brody; James L Mills
Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.
American journal of medical genetics. Part A 2011;155A(1):14-21.
2011: Sharon Hensley Alford; Colleen M McBride; Robert J Reid; Eric B Larson; Andreas D Baxevanis; Lawrence C Brody
Participation in genetic testing research varies by social group.
Public health genomics 2011;14(2):85-93.
2010: Faith Pangilinan; A Mitchell; J VanderMeer; Anne M Molloy; James F Troendle; Mary Conley; Peadar N Kirke; M Sutton; J M Sequeira; E V Quadros; John M Scott; James L Mills; Lawrence C Brody
Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects.
Journal of medical genetics 2010;47(10):677-85.
2010: Hui-Lee Wong; Ulrike Peters; Richard B Hayes; Wen-Yi Huang; Arthur Schatzkin; Robert S Bresalier; Ellen M Velie; Lawrence C Brody
Polymorphisms in the adenomatous polyposis coli (APC) gene and advanced colorectal adenoma risk.
European journal of cancer (Oxford, England : 1990) 2010;46(13):2457-66.
2010: Tonia C Carter; Anne M Molloy; Faith Pangilinan; James F Troendle; Peadar N Kirke; Mary R Conley; David Orr; Michael Earley; Eamon McKiernan; Ena C Lynn; Anne Doyle; John M Scott; Lawrence C Brody; James L Mills
Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.
Birth defects research. Part A, Clinical and molecular teratology 2010;88(2):84-93.
2010: Kimberly A Kaphingst; Colleen M McBride; Christopher Wade; Sharon Hensley Alford; Lawrence C Brody; Andreas D Baxevanis
Consumers' use of web-based information and their decisions about multiplex genetic susceptibility testing.
Journal of medical Internet research 2010;12(3):e41.
2009: Anne Parle-McDermott; Faith Pangilinan; Kirsty K O'Brien; James L Mills; Alan M Magee; James Troendle; Marie Sutton; John M Scott; Peadar N Kirke; Anne M Molloy; Lawrence C Brody
A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency.
Human mutation 2009;30(12):1650-6.
2009: Colleen M McBride; Sharon Hensley Alford; Robert J Reid; Eric B Larson; Andreas D Baxevanis; Lawrence C Brody
Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(8):582-7.
2009: Lavanya H Palavalli; Todd D Prickett; John R Wunderlich; Xiaomu Wei; Allison S Burrell; Patricia Porter-Gill; Sean Davis; Chenwei Wang; Julia C Cronin; Neena S Agrawal; Jimmy C Lin; Wendy Westbroek; Shelley Hoogstraten-Miller; Alfredo A Molinolo; Patricia Fetsch; Armando C Filie; Michael O'Connell; Carolyn E Banister; Jason D Howard; Phillip Buckhaults; Ashani T Weeraratna; Lawrence C Brody; STEVEN ROSENBERG; Yardena Samuels
Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma.
Nature genetics 2009;41(5):518-20.
2009: Anne M Molloy; Lawrence C Brody; James L Mills; John M Scott; Peadar N Kirke
The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.
Birth defects research. Part A, Clinical and molecular teratology 2009;85(4):285-94.
2009: Nicola Carroll; Faith Pangilinan; Anne M Molloy; James Troendle; James L Mills; Peadar N Kirke; Lawrence C Brody; John M Scott; Anne Parle-McDermott
Analysis of the MTHFD1 promoter and risk of neural tube defects.
Human genetics 2009;125(3):247-56.
2009: Anne M Molloy; Peadar N Kirke; James F Troendle; Helen Burke; Marie Sutton; Lawrence C Brody; John M Scott; James L Mills
Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification.
Pediatrics 2009;123(3):917-23.
2009: Adam Mitchell; Faith Pangilinan; Julie Van der Meer; Anne M Molloy; James Troendle; Mary Conley; Peadar N Kirke; John M Scott; Lawrence C Brody; James L Mills
Uncoupling protein 2 polymorphisms as risk factors for NTDs.
Birth defects research. Part A, Clinical and molecular teratology 2009;85(2):156-60.
2008: Faith Pangilinan; Kerry Geiler; Jessica Dolle; James Troendle; Deborah A Swanson; Anne M Molloy; Marie Sutton; Mary Conley; Peadar N Kirke; John M Scott; James L Mills; Lawrence C Brody
Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.
American journal of medical genetics. Part A 2008;146A(20):2617-25.
2008: James L Mills; Anne M Molloy; Anne Parle-McDermott; James F Troendle; Lawrence C Brody; Mary R Conley; Christopher Cox; Faith Pangilinan; David Orr; Michael Earley; Eamon McKiernan; Ena C Lynn; Anne Doyle; John M Scott; Peadar N Kirke
Folate-related gene polymorphisms as risk factors for cleft lip and cleft palate.
Birth defects research. Part A, Clinical and molecular teratology 2008;82(9):636-43.
2008: Colleen M McBride; Sharon Hensley Alford; Robert J Reid; Eric B Larson; Andreas D Baxevanis; Lawrence C Brody
Putting science over supposition in the arena of personalized genomics.
Nature genetics 2008;40(8):939-42.
2007: Colleen M McBride; Lawrence C Brody
Point: genetic risk feedback for common disease time to test the waters.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007;16(9):1724-6.
2007: Anne Parle-McDermott; Faith Pangilinan; James L Mills; Peadar N Kirke; Eileen R Gibney; James F Troendle; Valerie B O'Leary; Anne M Molloy; Mary Conley; John M Scott; Lawrence C Brody
The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population.
American journal of medical genetics. Part A 2007;143A(11):1174-80.
2007: Andrea K Lawrance; Liyuan Deng; Lawrence C Brody; Richard Finnell; Barry Shane; Rima Rozen
Genetic and nutritional deficiencies in folate metabolism influence tumorigenicity in Apcmin/+ mice.
The Journal of nutritional biochemistry 2007;18(5):305-12.
2006: Anne Parle-McDermott; James L Mills; Anne M Molloy; Nicola Carroll; Peadar N Kirke; Christopher Cox; Mary R Conley; Faith Pangilinan; Lawrence C Brody; John M Scott
The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels.
Molecular genetics and metabolism 2006;88(3):290-4.
2006: Anne Parle-McDermott; Peadar N Kirke; James L Mills; Anne M Molloy; Christopher Cox; Valerie B O'Leary; Faith Pangilinan; Mary Conley; Laura Cleary; Lawrence C Brody; John M Scott
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population.
European journal of human genetics : EJHG 2006;14(6):768-72.
2006: Valerie B O'Leary; Faith Pangilinan; Christopher Cox; Anne Parle-McDermott; Mary Conley; Anne M Molloy; Peadar N Kirke; James L Mills; Lawrence C Brody; John M Scott
Reduced folate carrier polymorphisms and neural tube defect risk.
Molecular genetics and metabolism 2006;87(4):364-9.
2005: Anne M Molloy; James L Mills; Christopher Cox; Sean Daly; Mary Conley; Lawrence C Brody; Peadar N Kirke; John M Scott; Per Magne Ueland
Choline and homocysteine interrelations in umbilical cord and maternal plasma at delivery.
The American journal of clinical nutrition 2005;82(4):836-42.
2005: Valerie B O'Leary; James L Mills; Anne Parle-McDermott; Faith Pangilinan; Anne M Molloy; Christopher Cox; Andrea Weiler; Mary Conley; Peadar N Kirke; John M Scott; Lawrence C Brody
Screening for new MTHFR polymorphisms and NTD risk.
American journal of medical genetics. Part A 2005;138A(2):99-106.
2005: Lawrence C Brody
Treating cancer by targeting a weakness.
The New England journal of medicine 2005;353(9):949-50.
2005: Anne Parle-McDermott; Faith Pangilinan; James L Mills; Caroline Signore; Anne M Molloy; Amanda Cotter; Mary Conley; Christopher Cox; Peadar N Kirke; John M Scott; Lawrence C Brody
A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss.
Molecular human reproduction 2005;11(7):477-80.
2005: Valerie B O'Leary; James L Mills; Faith Pangilinan; Peadar N Kirke; Christopher Cox; Mary Conley; Andrea Weiler; Kun Peng; Barry Shane; John M Scott; Anne Parle-McDermott; Anne M Molloy; Lawrence C Brody
Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.
Molecular genetics and metabolism 2005;85(3):220-7.
2005: James L Mills; Charlotte M Druschel; Faith Pangilinan; Kenneth Pass; Christopher Cox; Rebecca R Seltzer; Mary R Conley; Lawrence C Brody
Folate-related genes and omphalocele.
American journal of medical genetics. Part A 2005;136(1):8-11.
2005: Deborah A Swanson; Faith Pangilinan; James L Mills; Peadar N Kirke; Mary Conley; Andrea Weiler; Tiffany Frey; Anne Parle-McDermott; Valerie B O'Leary; Rebecca R Seltzer; Kathryn A Moynihan; Anne M Molloy; Helen Burke; John M Scott; Lawrence C Brody
Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population.
Birth defects research. Part A, Clinical and molecular teratology 2005;73(4):239-44.
2005: Anne Parle-McDermott; James L Mills; Peadar N Kirke; Christopher Cox; Caroline Signore; Sandra Kirke; Anne M Molloy; Valerie B O'Leary; Faith Pangilinan; Colm O'Herlihy; Lawrence C Brody; John M Scott
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae.
American journal of medical genetics. Part A 2005;132(4):365-8.
2004: Peadar N Kirke; James L Mills; Anne M Molloy; Lawrence C Brody; Valerie B O'Leary; Leslie Daly; Sharon Murray; Mary Conley; Philip D Mayne; Owen Smith; John M Scott
Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study.
BMJ (Clinical research ed.) 2004;328(7455):1535-6.
2004: Robert S Coyne; Heather B McDonald; Keith Edgemon; Lawrence C Brody
Functional characterization of BRCA1 sequence variants using a yeast small colony phenotype assay.
Cancer biology & therapy 2004;3(5):453-7.
2003: Anne Parle-McDermott; Edward J McManus; James L Mills; Valerie B O'Leary; Faith Pangilinan; Christopher Cox; Andrea Weiler; Anne M Molloy; Mary Conley; Deborah Watson; John M Scott; Lawrence C Brody; Peadar N Kirke
Polymorphisms within the vitamin B12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects.
Molecular genetics and metabolism 2003;80(4):463-8.
2003: Valerie B O'Leary; James L Mills; Peadar N Kirke; Anne Parle-McDermott; Deborah A Swanson; Andrea Weiler; Faith Pangilinan; Mary Conley; Anne M Molloy; Miriam Lynch; Christopher Cox; John M Scott; Lawrence C Brody
Analysis of the human folate receptor beta gene for an association with neural tube defects.
Molecular genetics and metabolism 2003;79(2):129-33.
2003: Anne Parle-McDermott; James L Mills; Peadar N Kirke; Valerie B O'Leary; Deborah A Swanson; Faith Pangilinan; Mary Conley; Anne M Molloy; Christopher Cox; John M Scott; Lawrence C Brody
Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects.
Journal of human genetics 2003;48(4):190-3.
2002: Lawrence C Brody; Mary Conley; Christopher Cox; Peadar N Kirke; Mary P McKeever; James L Mills; Anne M Molloy; Valerie B O'Leary; Anne Parle-McDermott; John M Scott; Deborah A Swanson
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.
American journal of human genetics 2002;71(5):1207-15.
2002: Patricia Hartge; Nilanjan Chatterjee; Sholom Wacholder; Lawrence C Brody; Margaret A Tucker; Jeffery Struewing
Breast cancer risk in Ashkenazi BRCA1/2 mutation carriers: effects of reproductive history.
Epidemiology (Cambridge, Mass.) 2002;13(3):255-61.
2002: Ronit I Yarden; Sherly Pardo-Reoyo; Magdalene K Sgagias; Kenneth H Cowan; Lawrence C Brody
BRCA1 regulates the G2/M checkpoint by activating Chk1 kinase upon DNA damage.
Nature genetics 2002;30(3):285-9.
2001: Charis Eng; Lawrence C Brody; Teresa M U Wagner; Peter Devilee; Jan Vijg; Csilla I Szabo; Sean V Tavtigian; Katherine L Nathanson; Elaine A Ostrander; Thomas S Frank
Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.
Journal of medical genetics 2001;38(12):824-33.
2001: Deborah A Swanson; M L Liu; P J Baker; Lisa J Garrett; M Stitzel; J Wu; M Harris; R Banerjee; Barry Shane; Lawrence C Brody
Targeted disruption of the methionine synthase gene in mice.
Molecular and cellular biology 2001;21(4):1058-65.
2001: Ronit I Yarden; Lawrence C Brody
Identification of proteins that interact with BRCA1 by Far-Western library screening.
Journal of cellular biochemistry 2001;83(4):521-31.
2000: Sharon Maor; Shirley Abramovitch; Michael R Erdos; Lawrence C Brody; Haim Werner
BRCA1 suppresses insulin-like growth factor-I receptor promoter activity: potential interaction between BRCA1 and Sp1.
Molecular genetics and metabolism 2000;69(2):130-6.
2000: Csilla I Szabo; A Masiello; J F Ryan; Lawrence C Brody
The breast cancer information core: database design, structure, and scope.
Human mutation 2000;16(2):123-31.
1999: Lawrence C Brody; P J Baker; Peter S Chines; A Musick; Anne M Molloy; Deborah A Swanson; Peadar N Kirke; S Ghosh; John M Scott; James L Mills
Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects.
Molecular genetics and metabolism 1999;67(4):324-33.
1999: Joseph G Hacia; Jian-Bing Fan; Oliver A Ryder; L Jin; Keith Edgemon; Ghassan Ghandour; R Aeryn Mayer; B Sun; Linda Hsie; Christiane M Robbins; Lawrence C Brody; D Wang; Eric S Lander; Rob Lipshutz; Steve Fodor; Francis S Collins
Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.
Nature genetics 1999;22(2):164-7.
1999: Ronit I Yarden; Lawrence C Brody
BRCA1 interacts with components of the histone deacetylase complex.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(9):4983-8.
1999: Patricia Hartge; Jeffery Struewing; Sholom Wacholder; Lawrence C Brody; Margaret A Tucker
The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews.
American journal of human genetics 1999;64(4):963-70.
1999: Jennifer Shuwen Lee; Sholom Wacholder; Jeffery Struewing; Mary McAdams; David Pee; Lawrence C Brody; Margaret A Tucker; Patricia Hartge
Survival after breast cancer in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.
Journal of the National Cancer Institute 1999;91(3):259-63.
1998: Joseph G Hacia; Lawrence C Brody; Francis S Collins
Applications of DNA chips for genomic analysis.
Molecular psychiatry 1998;3(6):483-92.
1998: T Woodage; S M King; Sholom Wacholder; Patricia Hartge; Jeffery Struewing; Mary McAdams; S J Laken; Margaret A Tucker; Lawrence C Brody
The APCI1307K allele and cancer risk in a community-based study of Ashkenazi Jews.
Nature genetics 1998;20(1):62-5.
1998: Mark Redston; Katherine L Nathanson; Ziqiang Yuan; Susan L Neuhausen; Jaya M Satagopan; Nora Wong; D Yang; D Nafa; JL Abrahamson; Hilmi Ozcelik; Danielle Antin-Ozerkis; Irene L Andrulis; M Daly; Leonard Pinsky; Deborah Schrag; S Gallinger; M Kaback; Mary-Claire King; T Woodage; Lawrence C Brody; A Godwin; Ellen Warner; Barbara Weber; William D Foulkes; Kenneth Offit
The APCI1307K allele and breast cancer risk.
Nature genetics 1998;20(1):13-4.
1998: Saijun Fan; Ji-An Wang; Ren-Qi Yuan; Yong Xian Ma; Qinghui Meng; Michael R Erdos; Lawrence C Brody; Itzhak D Goldberg; Eliot M Rosen
BRCA1 as a potential human prostate tumor suppressor: modulation of proliferation, damage responses and expression of cell regulatory proteins.
Oncogene 1998;16(23):3069-82.
1998: Lawrence C Brody; Barbara Bowles Biesecker
Breast cancer susceptibility genes. BRCA1 and BRCA2.
Medicine 1998;77(3):208-26.
1998: Joseph G Hacia; W Makalowski; Keith Edgemon; Michael R Erdos; Christiane M Robbins; Steve Fodor; Lawrence C Brody; Francis S Collins
Evolutionary sequence comparisons using high-density oligonucleotide arrays.
Nature genetics 1998;18(2):155-8.
1997: Lawrence C Brody; Barbara Bowles Biesecker
Breast cancer: the high-risk mutations.
Hospital practice (1995) 1997;32(10):59-63, 67-8, 70-2 passim.
1997: Jeff Humphrey; A Salim; Michael R Erdos; Francis S Collins; Lawrence C Brody; Richard D Klausner
Human BRCA1 inhibits growth in yeast: potential use in diagnostic testing.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(11):5820-5.
1997: Jeffery Struewing; Patricia Hartge; Sholom Wacholder; S M Baker; M Berlin; Mary McAdams; M M Timmerman; Lawrence C Brody; Margaret A Tucker
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews.
The New England journal of medicine 1997;336(20):1401-8.
1997: Barbara Bowles Biesecker; Lawrence C Brody
Genetic susceptibility testing for breast and ovarian cancer: a progress report.
Journal of the American Medical Women's Association (1972) 1997;52(1):22-7.
1996: Joseph G Hacia; Lawrence C Brody; M S Chee; Steve Fodor; Francis S Collins
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis.
Nature genetics 1996;14(4):441-7.
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.
1996: Carole Oddoux; Jeffery Struewing; C M Clayton; Susan L Neuhausen; Lawrence C Brody; M Kaback; B Haas; Larry Norton; Patrick I Borgen; Suresh C Jhanwar; David E Goldgar; Harry Ostrer; Kenneth Offit
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%.
Nature genetics 1996;14(2):188-90.
1996: Mark W Russell; S du Manoir; D J Munroe; Francis S Collins; Lawrence C Brody
Chromosomal localization of 15 ion channel genes.
Somatic cell and molecular genetics 1996;22(5):425-31.
1996: Mark W Russell; Macdonald Dick II; Francis S Collins; Lawrence C Brody
KVLQT1 mutations in three families with familial or sporadic long QT syndrome.
Human molecular genetics 1996;5(9):1319-24.
1996: Mark W Russell; D J Munroe; E Bric; David E Housman; J Dietz-Band; H C Riethman; Francis S Collins; Lawrence C Brody
A 500-kb physical map and contig from the Harvey ras-1 gene to the 11p telomere.
Genomics 1996;35(2):353-60.
1996: Jeffery Struewing; R E Tarone; Lawrence C Brody; Frederick P Li; J D Boice
BRCA1 mutations in young women with breast cancer.
Lancet 1996;347(9013):1493.
1996: E Schröck; P Badger; D Larson; Michael R Erdos; Anthony Wynshaw-Boris; Thomas Ried; Lawrence C Brody
The murine homolog of the human breast and ovarian cancer susceptibility gene Brca1 maps to mouse chromosome 11D.
Human genetics 1996;97(2):256-9.
1995: Jeffery Struewing; Dvorah Abeliovich; T Peretz; N Avishai; M M Kaback; Francis S Collins; Lawrence C Brody
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals.
Nature genetics 1995;11(2):198-200.
1995: P P Ho; Fergus J. Couch; Lawrence C Brody; K J Abel; Michael Boehnke; T H Shearon; Settara C Chandrasekharappa; Francis S Collins; Barbara L Weber
Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3.
Somatic cell and molecular genetics 1995;21(5):351-5.
1995: Mark W Russell; Macdonald Dick II; R M Campbell; J E Hulse; D J Munroe; E Bric; David E Housman; Francis S Collins; Lawrence C Brody
Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349.
American journal of human genetics 1995;57(2):503-7.
1995: Jeffery Struewing; Lawrence C Brody; Michael R Erdos; R G Kase; T R Giambarresi; S A Smith; Francis S Collins; Margaret A Tucker
Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer.
American journal of human genetics 1995;57(1):1-7.
1995: Fergus J. Couch; Lucio H Castilla; Jianfeng Xu; K J Abel; Piri Welcsh; S E King; L Wong; P P Ho; Sofia D Merajver; Lawrence C Brody
A YAC-, P1-, and cosmid-based physical map of the BRCA1 region on chromosome 17q21.
Genomics 1995;25(1):264-73.
1995: Lawrence C Brody; K J Abel; Lucio H Castilla; Fergus J. Couch; D R McKinley; G Yin; P P Ho; Sofia D Merajver; Settara C Chandrasekharappa; Jianfeng Xu
Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17.
Genomics 1995;25(1):238-47.
1995: Barbara L Weber; K J Abel; Fergus J. Couch; Sofia D Merajver; Lucio H Castilla; Lawrence C Brody; Francis S Collins
Transcript identification in the BRCA1 candidate region.
Breast cancer research and treatment 1995;33(2):115-24.
1994: Lucio H Castilla; Fergus J. Couch; Michael R Erdos; K F Hoskins; Kathleen A Calzone; Judy E Garber; J Boyd; M B Lubin; M L Deshano; Lawrence C Brody
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer.
Nature genetics 1994;8(4):387-91.
1994: Barbara L Weber; K J Abel; Lawrence C Brody; W L Flejter; Settara C Chandrasekharappa; Fergus J. Couch; Sofia D Merajver; Francis S Collins
Familial breast cancer. Approaching the isolation of a susceptibility gene.
Cancer 1994;74(3 Suppl):1013-20.
1994: Fergus J. Couch; K J Abel; Lawrence C Brody; Michael Boehnke; Francis S Collins; Barbara L Weber
Localization of the gene for ATP citrate lyase (ACLY) distal to gastrin(GAS) and proximal to D17S856 on chromosome 17q12-q21.
Genomics 1994;21(2):444-6.