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Jeffrey C Murray
Jeffrey C Murray
Professor of Pediatrics, University of Iowa
Verified email at uiowa.edu
Title
Cited by
Cited by
Year
Genetic studies of body mass index yield new insights for obesity biology
AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ...
Nature 518 (7538), 197, 2015
45812015
Cleft lip and palate: understanding genetic and environmental influences
MJ Dixon, ML Marazita, TH Beaty, JC Murray
Nature Reviews Genetics 12 (3), 167-178, 2011
21332011
Comprehensive human genetic maps: individual and sex-specific variation in recombination
KW Broman, JC Murray, VC Sheffield, RL White, JL Weber
The American Journal of Human Genetics 63 (3), 861-869, 1998
12991998
Developmental Biology: Frontiers for Clinical Genetics. Gene/environment causes of cleft lip and/or palate
JC Murray
Clinical Genetics 61 (4), 248-256, 2002
10982002
Gene/environment causes of cleft lip and/or palate
JC Murray
Clinical genetics 61 (4), 248-256, 2002
10732002
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
EV Semina, R Reiter, NJ Leysens, WLM Alward, KW Small, NA Datson, ...
Nature genetics 14 (4), 392-399, 1996
10661996
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
S Kondo, BC Schutte, RJ Richardson, BC Bjork, AS Knight, Y Watanabe, ...
Nature genetics 32 (2), 285-289, 2002
10472002
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
TM Zucchero, ME Cooper, BS Maher, S Daack-Hirsch, B Nepomuceno, ...
New England Journal of Medicine 351 (8), 769-780, 2004
7722004
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)
JC Murray, KH Buetow, JL Weber, S Ludwigsen, T Scherpbier-Heddema, ...
Science 265 (5181), 2049-2054, 1994
7101994
Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
TH Beaty, JC Murray, ML Marazita, RG Munger, IRJB Hetmanski, ...
Nature Genetics 42 (8), 727-727, 2010
664*2010
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
TH Beaty, JC Murray, ML Marazita, RG Munger, I Ruczinski, JB Hetmanski, ...
Nature genetics 42 (6), 525-529, 2010
6602010
Detectable clonal mosaicism from birth to old age and its relationship to cancer
CC Laurie, CA Laurie, K Rice, KF Doheny, LR Zelnick, CP McHugh, ...
Nature genetics 44 (6), 642-650, 2012
6332012
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
CE Elks, JRB Perry, P Sulem, DI Chasman, N Franceschini, C He, ...
Nature genetics 42 (12), 1077-1085, 2010
6032010
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate.
HH Ardinger, KH Buetow, GI Bell, J Bardach, DR VanDemark, JC Murray
American journal of human genetics 45 (3), 348, 1989
5421989
Non-invasive whole genome sequencing of a human fetus
JO Kitzman, MW Snyder, M Ventura, AP Lewis, R Qiu, LE Simmons, ...
Science translational medicine 4 (137), 137ra76-137ra76, 2012
5112012
The many faces and factors of orofacial clefts
BC Schutte, JC Murray
Human molecular genetics 8 (10), 1853-1859, 1999
5071999
Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
F Rahimov, ML Marazita, A Visel, ME Cooper, MJ Hitchler, M Rubini, ...
Nature genetics 40 (11), 1341-1347, 2008
4862008
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans
AC Lidral, PA Romitti, AM Basart, T Doetschman, NJ Leysens, ...
The American Journal of Human Genetics 63 (2), 557-568, 1998
4701998
Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants.
GM Shaw, CR Wasserman, EJ Lammer, CD O'Malley, JC Murray, ...
American journal of human genetics 58 (3), 551, 1996
4661996
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
EV Semina, RE Ferrell, HA Mintz-Hittner, P Bitoun, WLM Alward, ...
Nature genetics 19 (2), 167-170, 1998
4411998
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