Val C. Sheffield, M.D., Ph.D.
Val C. Sheffield, M.D., Ph.D.
Investigator, Howard Hughes Medical Institute, Professor of Pediatrics, University of Iowa
Verified email at uiowa.edu
Title
Cited by
Cited by
Year
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
18652010
Attachment of a 40-base-pair G+ C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes
VC Sheffield, DR Cox, LS Lerman, RM Myers
Proceedings of the National Academy of Sciences 86 (1), 232-236, 1989
16291989
Identification of a gene that causes primary open angle glaucoma
EM Stone, JH Fingert, WLM Alward, TD Nguyen, JR Polansky, ...
Science 275 (5300), 668-670, 1997
15181997
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
14282007
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
LA Everett, B Glaser, JC Beck, JR Idol, A Buchs, F Adawi, E Hazani, ...
Nature genetics 17 (4), 411-422, 1997
12401997
A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis
MV Nachury, AV Loktev, Q Zhang, CJ Westlake, J Peränen, A Merdes, ...
Cell 129 (6), 1201-1213, 2007
11932007
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
11911998
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions
VC Sheffield, JS Beck, AE Kwitek, DW Sandstrom, EM Stone
Genomics 16 (2), 325-332, 1993
8571993
The Pendred syndrome gene encodes a chloride-iodide transport protein
DA Scott, R Wang, TM Kreman, VC Sheffield, LP Karniski
Nature genetics 21 (4), 440-443, 1999
6781999
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
6611994
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking
Nature 461 (7265), 802-808, 2009
6422009
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations
JH Fingert, E Héon, JM Liebmann, T Yamamoto, JE Craig, J Rait, ...
Human molecular genetics 8 (5), 899-905, 1999
6181999
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
5802010
Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31
VC Sheffield, EM Stone, WLM Alward, AV Drack, AT Johnson, LM Streb, ...
Nature genetics 4 (1), 47-50, 1993
5461993
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia
RY Walder, D Landau, P Meyer, H Shalev, M Tsolia, Z Borochowitz, ...
Nature genetics 31 (2), 171-174, 2002
5432002
Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer
WM Grady, J Willis, PJ Guilford, AK Dunbier, TT Toro, H Lynch, G Wiesner, ...
Nature genetics 26 (1), 16-17, 2000
4852000
Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A)
WLM Alward, JH Fingert, MA Coote, AT Johnson, SF Lerner, D Junqua, ...
New England Journal of Medicine 338 (15), 1022-1027, 1998
4821998
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways
L Sang, JJ Miller, KC Corbit, RH Giles, MJ Brauer, EA Otto, LM Baye, ...
Cell 145 (4), 513-528, 2011
4812011
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
DY Nishimura, RE Swiderski, WLM Alward, CC Searby, SR Patil, ...
Nature genetics 19 (2), 140-147, 1998
4751998
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness
GE Green, DA Scott, JM McDonald, GG Woodworth, VC Sheffield, ...
Jama 281 (23), 2211-2216, 1999
4601999
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