受强制性开放获取政策约束的文章 - DAVID J CUTLER了解详情
无法在其他位置公开访问的文章：2 篇
查看
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes
SW Curtis, JC Carlson, TH Beaty, JC Murray, SM Weinberg, ML Marazita, ...
Human genetics 142 (10), 1531-1541, 2023
强制性开放获取政策： US National Institutes of Health
查看
A159: the autoimmune genetic architecture of childhood onset rheumatoid arthritis
S Prahalad, MC Marion, J Cobb, M Sudman, A Hinks, M Pichavant, ...
Arthritis & Rheumatology 66, S205-S206, 2014
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：102 篇
查看
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...
Nature 515 (7526), 209-215, 2014
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, Health …
查看
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
强制性开放获取政策： US National Science Foundation, US National Institutes of Health, Autism …
查看
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
JA Kosmicki, KE Samocha, DP Howrigan, SJ Sanders, K Slowikowski, ...
Nature genetics 49 (4), 504-510, 2017
强制性开放获取政策： US National Institutes of Health
查看
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
强制性开放获取政策： US National Science Foundation, US National Institutes of Health, Autism …
查看
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13. 2
FA Wright, LJ Strug, VK Doshi, CW Commander, SM Blackman, L Sun, ...
Nature genetics 43 (6), 539-546, 2011
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
查看
Autosomal recessive causes likely in early-onset Alzheimer disease
TS Wingo, JJ Lah, AI Levey, DJ Cutler
Archives of neurology 69 (1), 59-64, 2012
强制性开放获取政策： US National Institutes of Health
查看
Microdeletions of 3q29 confer high risk for schizophrenia
JG Mulle, AF Dodd, JA McGrath, PS Wolyniec, AA Mitchell, AC Shetty, ...
The American Journal of Human Genetics 87 (2), 229-236, 2010
强制性开放获取政策： US National Institutes of Health
查看
Family-based association of FKBP5 in bipolar disorder
VL Willour, H Chen, J Toolan, P Belmonte, DJ Cutler, FS Goes, PP Zandi, ...
Molecular psychiatry 14 (3), 261-268, 2009
强制性开放获取政策： US National Institutes of Health
查看
Recessive gene disruptions in autism spectrum disorder
RN Doan, ET Lim, S De Rubeis, C Betancur, DJ Cutler, AG Chiocchetti, ...
Nature genetics 51 (7), 1092-1098, 2019
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, UK …
查看
Genome-wide association study identifies African-specific susceptibility loci in African Americans with inflammatory bowel disease
SR Brant, DT Okou, CL Simpson, DJ Cutler, T Haritunians, JP Bradfield, ...
Gastroenterology 152 (1), 206-217. e2, 2017
强制性开放获取政策： US National Institutes of Health
查看
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males
SC Collins, SM Bray, JA Suhl, DJ Cutler, B Coffee, ME Zwick, ST Warren
American journal of medical genetics Part A 152 (10), 2512-2520, 2010
强制性开放获取政策： US National Institutes of Health
查看
Genetic contributors to risk of schizophrenia in the presence of a 22q11. 2 deletion
I Cleynen, W Engchuan, MS Hestand, T Heung, AM Holleman, ...
Molecular psychiatry 26 (8), 4496-4510, 2021
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health …
查看
Association of early-onset Alzheimer disease with elevated low-density lipoprotein cholesterol levels and rare genetic coding variants of APOB
TS Wingo, DJ Cutler, AP Wingo, NA Le, GD Rabinovici, BL Miller, JJ Lah, ...
JAMA neurology 76 (7), 809-817, 2019
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, State …
查看
Blood-derived DNA methylation signatures of Crohn's disease and severity of intestinal inflammation
HK Somineni, S Venkateswaran, V Kilaru, UM Marigorta, A Mo, DT Okou, ...
Gastroenterology 156 (8), 2254-2265. e3, 2019
强制性开放获取政策： US National Institutes of Health
查看
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility
A Sazonovs, CR Stevens, GR Venkataraman, K Yuan, B Avila, MT Abreu, ...
Nature genetics 54 (9), 1275-1283, 2022
强制性开放获取政策： US National Institutes of Health, Academy of Finland, UK Medical Research …
查看
Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans
C Huang, T Haritunians, DT Okou, DJ Cutler, ME Zwick, KD Taylor, ...
Gastroenterology 149 (6), 1575-1586, 2015
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, Natural …
查看
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11. 23 is associated with schizophrenia
JG Mulle, AE Pulver, JA McGrath, PS Wolyniec, AF Dodd, DJ Cutler, ...
Biological psychiatry 75 (5), 371-377, 2014
强制性开放获取政策： US National Institutes of Health, Swedish Research Council, UK Medical …
查看
Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis
LA Bremer, SM Blackman, LL Vanscoy, KE McDougal, A Bowers, ...
Human molecular genetics 17 (14), 2228-2237, 2008
强制性开放获取政策： US National Institutes of Health
出版信息和资助信息由计算机程序自动确定