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Nicholas Schork
Nicholas Schork
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Alıntı yapanlar
Alıntı yapanlar
Yıl
Genetic dissection of complex traits
ES Lander, NJ Schork
Focus 265 (3), 2037-458, 2006
46182006
Identification of ALK as a major familial neuroblastoma predisposition gene
YP Mossé, M Laudenslager, L Longo, KA Cole, A Wood, EF Attiyeh, ...
Nature 455 (7215), 930-935, 2008
16362008
Standard-vs high-dose clopidogrel based on platelet function testing after percutaneous coronary intervention: the GRAVITAS randomized trial
MJ Price, PB Berger, PS Teirstein, JF Tanguay, DJ Angiolillo, D Spriggs, ...
Jama 305 (11), 1097-1105, 2011
16212011
Family income, parental education and brain structure in children and adolescents
KG Noble, SM Houston, NH Brito, H Bartsch, E Kan, JM Kuperman, ...
Nature neuroscience 18 (5), 773-778, 2015
15692015
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Nature genetics 43 (10), 977-983, 2011
14772011
Human genetic variation and its contribution to complex traits
KA Frazer, SS Murray, NJ Schork, EJ Topol
Nature Reviews Genetics 10 (4), 241-251, 2009
13892009
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
13682019
Personalized medicine: time for one-person trials
NJ Schork
Nature 520 (7549), 609-611, 2015
12542015
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
R Knöll, M Hoshijima, HM Hoffman, V Person, I Lorenzen-Schmidt, ...
Cell 111 (7), 943-955, 2002
9412002
Histopathology of pediatric nonalcoholic fatty liver disease
JB Schwimmer, C Behling, R Newbury, R Deutsch, C Nievergelt, ...
Hepatology 42 (3), 641-649, 2005
9272005
Common vs. rare allele hypotheses for complex diseases
NJ Schork, SS Murray, KA Frazer, EJ Topol
Current opinion in genetics & development 19 (3), 212-219, 2009
8922009
Gut microbiome-based metagenomic signature for non-invasive detection of advanced fibrosis in human nonalcoholic fatty liver disease
R Loomba, V Seguritan, W Li, T Long, N Klitgord, A Bhatt, PS Dulai, ...
Cell metabolism 25 (5), 1054-1062. e5, 2017
8892017
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
HJ Watson, Z Yilmaz, LM Thornton, C Hübel, JRI Coleman, HA Gaspar, ...
Nature genetics 51 (8), 1207-1214, 2019
7822019
Evaluation of next generation sequencing platforms for population targeted sequencing studies
O Harismendy, PC Ng, RL Strausberg, X Wang, TB Stockwell, KY Beeson, ...
Genome biology 10, 1-13, 2009
7722009
Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment
JM Drazen, CN Yandava, L Dubé, N Szczerback, R Hippensteel, A Pillari, ...
Nature genetics 22 (2), 168-170, 1999
7441999
The n-of-1 clinical trial: the ultimate strategy for individualizing medicine?
EO Lillie, B Patay, J Diamant, B Issell, EJ Topol, NJ Schork
Personalized medicine 8 (2), 161-173, 2011
6982011
Transgenerational epigenetic instability is a source of novel methylation variants
RJ Schmitz, MD Schultz, MG Lewsey, RC O’Malley, MA Urich, O Libiger, ...
Science 334 (6054), 369-373, 2011
6872011
Genetic structure, self-identified race/ethnicity, and confounding in case-control association studies
H Tang, T Quertermous, B Rodriguez, SLR Kardia, X Zhu, A Brown, ...
The American Journal of Human Genetics 76 (2), 268-275, 2005
6592005
Longitudinal magnetic resonance imaging study of cortical development through early childhood in autism
CM Schumann, CS Bloss, CC Barnes, GM Wideman, RA Carper, ...
Journal of Neuroscience 30 (12), 4419-4427, 2010
6302010
Epigenomic diversity in a global collection of Arabidopsis thaliana accessions
T Kawakatsu, SSC Huang, F Jupe, E Sasaki, RJ Schmitz, MA Urich, ...
Cell 166 (2), 492-505, 2016
6262016
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