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Chris Gunter
Chris Gunter
National Human Genome Research Institute
Verified email at nih.gov - Homepage
Title
Cited by
Cited by
Year
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium
Nature 489 (7414), 57, 2012
138282012
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium Overall coordination (data analysis coordination ...
Nature 489 (7414), 57-74, 2012
30602012
International network of cancer genome projects
Data coordination centre Kasprzyk (Leader) Arek 1 Stein (Leader) Lincoln D ...
Nature 464 (7291), 993-998, 2010
22472010
Replicating genotype–phenotype associations
Nature 447 (7145), 655-660, 2007
16082007
Guidelines for investigating causality of sequence variants in human disease
DG MacArthur, TA Manolio, DP Dimmock, HL Rehm, J Shendure, ...
Nature 508 (7497), 469-476, 2014
13822014
Diversity in clinical and biomedical research: a promise yet to be fulfilled
SS Oh, J Galanter, N Thakur, M Pino-Yanes, NE Barcelo, MJ White, ...
PLoS medicine 12 (12), e1001918, 2015
5812015
Strategic vision for improving human health at The Forefront of Genomics
ED Green, C Gunter, LG Biesecker, V Di Francesco, CL Easter, ...
Nature 586 (7831), 683-692, 2020
2352020
Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein
V Brown, K Small, L Lakkis, Y Feng, C Gunter, KD Wilkinson, ST Warren
Journal of Biological Chemistry 273 (25), 15521-15527, 1998
2271998
Prepublication data sharing
Toronto International Data Release Workshop Authors
Nature 461 (7261), 168-170, 2009
2132009
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
X Zhou, P Feliciano, C Shu, T Wang, I Astrovskaya, JB Hall, JU Obiajulu, ...
Nature genetics 54 (9), 1305-1319, 2022
1282022
Epigenetics
A Eccleston, N DeWitt, C Gunter, B Marte, D Nath
Nature 447 (7143), 395-396, 2007
1212007
Normal variation at the myotonic dystrophy locus in global human populations.
C Zerylnick, A Torroni, SL Sherman, ST Warren
American journal of human genetics 56 (1), 123, 1995
1191995
FMR1 in global populations.
CB Kunst, C Zerylnick, L Karickhoff, E Eichler, J Bullard, M Chalifoux, ...
American journal of human genetics 58 (3), 513, 1996
941996
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1
C Gunter, W Paradee, DC Crawford, KA Meadows, J Newman, CB Kunst, ...
Human molecular genetics 7 (12), 1935-1946, 1998
871998
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population
DC Crawford, CE Schwartz, KL Meadows, JL Newman, LF Taft, C Gunter, ...
The American Journal of Human Genetics 66 (2), 480-493, 2000
652000
International network of cancer genome projects
W Anderson, A Aretz, AD Barker, C Bell, RR Bernabé, MK Bhan, F Calvo, ...
Nature 464 (7291), 993-998, 2010
602010
Human biology by proxy
C Gunter, R Dhand
Nature 420 (6915), 509-510, 2002
602002
Psychiatric and medical profiles of autistic adults in the SPARK cohort
E Fombonne, LA Green Snyder, A Daniels, P Feliciano, W Chung
Journal of autism and developmental disorders 50 (10), 3679-3698, 2020
432020
Beliefs in vaccine as causes of autism among SPARK cohort caregivers
E Fombonne, RP Goin-Kochel, BJ O'Roak, L Abbeduto, G Aberbach, ...
Vaccine 38 (7), 1794-1803, 2020
272020
She moves in mysterious ways
C Gunter
Nature 434 (7031), 279-280, 2005
272005
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