Dheeraj Malhotra
Dheeraj Malhotra
Unknown affiliation
Verified email at roche.com
Cited by
Cited by
Strong association of de novo copy number mutations with autism
J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ...
Science 316 (5823), 445-449, 2007
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
T Walsh, JM McClellan, SE McCarthy, AM Addington, SB Pierce, ...
science 320 (5875), 539-543, 2008
CNVs: harbingers of a rare variant revolution in psychiatric genetics
D Malhotra, J Sebat
Cell 148 (6), 1223-1241, 2012
Microduplications of 16p11. 2 are associated with schizophrenia
SE McCarthy, V Makarov, G Kirov, AM Addington, J McClellan, S Yoon, ...
Nature genetics 41 (11), 1223-1227, 2009
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation
JJ Michaelson, Y Shi, M Gujral, H Zheng, D Malhotra, X Jin, M Jian, G Liu, ...
Cell 151 (7), 1431-1442, 2012
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27-35, 2017
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
V Vacic, S McCarthy, D Malhotra, F Murray, HH Chou, A Peoples, ...
Nature 471 (7339), 499-503, 2011
High frequencies of de novo CNVs in bipolar disorder and schizophrenia
D Malhotra, S McCarthy, JJ Michaelson, V Vacic, KE Burdick, S Yoon, ...
Neuron 72 (6), 951-963, 2011
Altered human oligodendrocyte heterogeneity in multiple sclerosis
S Jškel, E Agirre, AM Falc„o, D Van Bruggen, KW Lee, I Knuesel, ...
Nature 566 (7745), 543-547, 2019
Leprosy and the adaptation of human toll-like receptor 1
SH Wong, S Gochhait, D Malhotra, FH Pettersson, YY Teo, CC Khor, ...
PLoS pathogens 6 (7), e1000979, 2010
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism
R Corominas, X Yang, GN Lin, S Kang, Y Shen, L Ghamsari, M Broly, ...
Nature communications 5 (1), 1-12, 2014
Progress in understanding and treating SCN2A-mediated disorders
SJ Sanders, AJ Campbell, JR Cottrell, RS Moller, FF Wagner, ...
Trends in neurosciences 41 (7), 442-456, 2018
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
AS Nord, W Roeb, DE Dickel, T Walsh, M Kusenda, KL O'connor, ...
European Journal of Human Genetics 19 (6), 727-731, 2011
Translating genome-wide association findings into new therapeutics for psychiatry
G Breen, Q Li, BL Roth, P O'donnell, M Didriksen, R Dolmetsch, PF O'reilly, ...
Nature neuroscience 19 (11), 1392-1396, 2016
IL-10 promoter single nucleotide polymorphisms are significantly associated with resistance to leprosy
D Malhotra, K Darvishi, S Sood, S Sharma, C Grover, V Relhan, ...
Human genetics 118 (2), 295-300, 2005
TLR2 Arg677Trp polymorphism in leprosy: revisited
D Malhotra, V Relhan, BSN Reddy, R Bamezai
Human genetics 116 (5), 413-415, 2005
Frequency and complexity of de novo structural mutation in autism
WM Brandler, D Antaki, M Gujral, A Noor, G Rosanio, TR Chapman, ...
The American Journal of Human Genetics 98 (4), 667-679, 2016
Genomewide association study of leprosy
SH Wong, AVS Hill, FO Vannberg, FR Zhang, W Huang, SM Chen, ...
New England Journal of Medicine 362 (15), 1446, 2010
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
Implication of a rare deletion at distal 16p11. 2 in schizophrenia
S Guha, E Rees, A Darvasi, D Ivanov, M Ikeda, SE Bergen, ...
JAMA psychiatry 70 (3), 253-260, 2013
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