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Jonathan Bradfield
Jonathan Bradfield
President, Quantinuum Research LLC
Verified email at quantinuumresearch.com
Title
Cited by
Cited by
Year
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
29262011
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ...
Nature 459 (7246), 569-573, 2009
15902009
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13472018
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
11162009
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
H Hakonarson, SFA Grant, JP Bradfield, L Marchand, CE Kim, ...
Nature 448 (7153), 591-594, 2007
6412007
Common variants at five new loci associated with early-onset inflammatory bowel disease
M Imielinski, RN Baldassano, A Griffiths, RK Russell, V Annese, ...
Nature genetics 41 (12), 1335-1340, 2009
5732009
A genome-wide association meta-analysis identifies new childhood obesity loci
Nature genetics 44 (5), 526-531, 2012
4912012
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
M Bucan, BS Abrahams, K Wang, JT Glessner, EI Herman, LI Sonnenblick, ...
PLoS genetics 5 (6), e1000536, 2009
4862009
Genome-wide associations for birth weight and correlations with adult disease
M Horikoshi, RN Beaumont, FR Day, NM Warrington, MN Kooijman, ...
Nature 538 (7624), 248-252, 2016
4552016
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ø Helgeland, ...
Nature genetics 51 (5), 804-814, 2019
4472019
Copy number variation at 1q21. 1 associated with neuroblastoma
SJ Diskin, C Hou, JT Glessner, EF Attiyeh, M Laudenslager, K Bosse, ...
Nature 459 (7249), 987-991, 2009
4392009
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications
TH Shaikh, X Gai, JC Perin, JT Glessner, H Xie, K Murphy, R O'Hara, ...
Genome research 19 (9), 1682-1690, 2009
4302009
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder
J Elia, JT Glessner, K Wang, N Takahashi, CJ Shtir, D Hadley, ...
Nature genetics 44 (1), 78-84, 2012
4192012
Variants of DENND1B Associated with Asthma in Children
PMA Sleiman, J Flory, M Imielinski, JP Bradfield, K Annaiah, ...
New England journal of medicine 362 (1), 36-44, 2010
4102010
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
S Kugathasan, RN Baldassano, JP Bradfield, PMA Sleiman, M Imielinski, ...
Nature genetics 40 (10), 1211-1215, 2008
4062008
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci
JP Bradfield, HQ Qu, K Wang, H Zhang, PM Sleiman, CE Kim, FD Mentch, ...
PLoS genetics 7 (9), e1002293, 2011
3852011
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
3792021
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease
K Wang, H Zhang, S Kugathasan, V Annese, JP Bradfield, RK Russell, ...
The American Journal of Human Genetics 84 (3), 399-405, 2009
3392009
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
M Capasso, M Devoto, C Hou, S Asgharzadeh, JT Glessner, EF Attiyeh, ...
Nature genetics 41 (6), 718-723, 2009
3362009
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
M Horikoshi, H Yaghootkar, DO Mook-Kanamori, U Sovio, HR Taal, ...
Nature genetics 45 (1), 76-82, 2013
3222013
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