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Sheng Chih Jin
Sheng Chih Jin
Assistant Professor of Genetics at Washington University School of Medicine
Verified email at wustl.edu - Homepage
Title
Cited by
Cited by
Year
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
TH Beaty, JC Murray, ML Marazita, RG Munger, I Ruczinski, JB Hetmanski, ...
Nature genetics 42 (6), 525-529, 2010
5992010
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies
J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ...
Science 350 (6265), 1262-1266, 2015
5762015
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ...
Nature genetics 49 (11), 1593-1601, 2017
5152017
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease
C Cruchaga, CM Karch, SC Jin, BA Benitez, Y Cai, R Guerreiro, O Harari, ...
Nature 505 (7484), 550-554, 2014
4642014
GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer’s disease
C Cruchaga, JSK Kauwe, O Harari, SC Jin, Y Cai, CM Karch, BA Benitez, ...
Neuron 78 (2), 256-268, 2013
3282013
Genome-wide and candidate gene association study of cigarette smoking behaviors
N Caporaso, F Gu, N Chatterjee, J Sheng-Chih, K Yu, M Yeager, C Chen, ...
PloS one 4 (2), e4653, 2009
2812009
A common haplotype lowers PU. 1 expression in myeloid cells and delays onset of Alzheimer's disease
K Huang, E Marcora, AA Pimenova, AF Di Narzo, M Kapoor, SC Jin, ...
Nature neuroscience 20 (8), 1052-1061, 2017
2782017
Coding variants in TREM2 increase risk for Alzheimer's disease
SC Jin, BA Benitez, CM Karch, B Cooper, T Skorupa, D Carrell, JB Norton, ...
Human molecular genetics 23 (21), 5838-5846, 2014
2482014
Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate
TH Beaty, I Ruczinski, JC Murray, ML Marazita, RG Munger, JB Hetmanski, ...
Genetic epidemiology 35 (6), 469-478, 2011
1932011
Alzheimer's disease‐associated TREM2 variants exhibit either decreased or increased ligand‐dependent activation
W Song, B Hooli, K Mullin, SC Jin, M Cella, TK Ulland, Y Wang, RE Tanzi, ...
Alzheimer's & Dementia 13 (4), 381-387, 2017
1662017
CLCN2 chloride channel mutations in familial hyperaldosteronism type II
UI Scholl, G Stölting, J Schewe, A Thiel, H Tan, C Nelson-Williams, ...
Nature genetics 50 (3), 349-354, 2018
1642018
TREM2 is associated with the risk of Alzheimer's disease in Spanish population
BA Benitez, B Cooper, P Pastor, SC Jin, E Lorenzo, S Cervantes, ...
Neurobiology of aging 34 (6), 1711. e15-1711. e17, 2013
1602013
TREM2 is associated with increased risk for Alzheimer’s disease in African Americans
SC Jin, MM Carrasquillo, BA Benitez, T Skorupa, D Carrell, D Patel, ...
Molecular neurodegeneration 10 (1), 1-7, 2015
1282015
Missense variant in TREML2 protects against Alzheimer's disease
BA Benitez, SC Jin, R Guerreiro, R Graham, J Lord, D Harold, R Sims, ...
Neurobiology of aging 35 (6), 1510. e19-1510. e26, 2014
1212014
Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort
SC Jin, P Pastor, B Cooper, S Cervantes, BA Benitez, C Razquin, A Goate, ...
Alzheimer's research & therapy 4 (4), 1-9, 2012
1002012
De novo mutation in genes regulating neural stem cell fate in human congenital hydrocephalus
CG Furey, J Choi, SC Jin, X Zeng, AT Timberlake, C Nelson-Williams, ...
Neuron 99 (2), 302-314. e4, 2018
772018
De novo pathogenic variants in CACNA1E cause developmental and epileptic encephalopathy with contractures, macrocephaly, and dyskinesias
KL Helbig, RJ Lauerer, JC Bahr, IA Souza, CT Myers, B Uysal, N Schwarz, ...
The American Journal of Human Genetics 103 (5), 666-678, 2018
742018
The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers
BA Benitez, CM Karch, Y Cai, SC Jin, B Cooper, D Carrell, S Bertelsen, ...
PLoS genetics 9 (8), e1003685, 2013
712013
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
SC Jin, SA Lewis, S Bakhtiari, X Zeng, MC Sierant, S Shetty, SM Nordlie, ...
Nature genetics 52 (10), 1046-1056, 2020
702020
Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson’s Disease
BA Benitez, AA Davis, SC Jin, L Ibanez, S Ortega-Cubero, P Pastor, ...
Molecular neurodegeneration 11 (1), 1-12, 2016
572016
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