Saurav Guha, PhD, FACMG
Saurav Guha, PhD, FACMG
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Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)
T Lencz, E Knowles, G Davies, S Guha, DC Liewald, JM Starr, S Djurovic, ...
Molecular psychiatry 19 (2), 168-174, 2014
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
S Carmi, KY Hui, E Kochav, X Liu, J Xue, F Grady, S Guha, K Upadhyay, ...
Nature communications 5 (1), 1-9, 2014
High rate of disease-related copy number variations in childhood onset schizophrenia
K Ahn, N Gotay, TM Andersen, AA Anvari, P Gochman, Y Lee, S Sanders, ...
Molecular psychiatry 19 (5), 568-572, 2014
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder
T Lencz, S Guha, C Liu, J Rosenfeld, S Mukherjee, P DeRosse, M John, ...
Nature communications 4 (1), 1-10, 2013
A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis
L Imundo, CA LeDuc, S Guha, M Brown, G Perino, L Gushulak, ...
Journal of inherited metabolic disease 34 (5), 1013-1022, 2011
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, 1-8, 2013
De novo copy number variants are associated with congenital diaphragmatic hernia
L Yu, J Wynn, L Ma, S Guha, GB Mychaliska, TM Crombleholme, ...
Journal of medical genetics 49 (10), 650-659, 2012
Molecular phylogeny of musk deer: a genomic view with mitochondrial 16S rRNA and cytochrome b gene
S Guha, SP Goyal, VK Kashyap
Molecular phylogenetics and evolution 42 (3), 585-597, 2007
Association of ApoE genetic variants with obstructive sleep apnea in children
M Kalra, P Pal, R Kaushal, RS Amin, LM Dolan, K Fitz, S Kumar, X Sheng, ...
Sleep medicine 9 (3), 260-265, 2008
Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry
P Pal, H Xi, S Guha, G Sun, BT Helfand, JJ Meeks, BK Suarez, ...
The Prostate 69 (14), 1548-1556, 2009
Genetic structure of Indian populations based on fifteen autosomal microsatellite loci
VK Kashyap, S Guha, T Sitalaximi, GH Bindu, SE Hasnain, R Trivedi
BMC genetics 7 (1), 1-9, 2006
Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin
P Pal, H Xi, G Sun, R Kaushal, JJ Meeks, CS Thaxton, S Guha, CH Jin, ...
Human genetics 122 (3), 251-259, 2007
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes
V Vacic, LJ Ozelius, LN Clark, A Bar-Shira, M Gana-Weisz, T Gurevich, ...
Human molecular genetics 23 (17), 4693-4702, 2014
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population
S Guha, JA Rosenfeld, AK Malhotra, AT Lee, PK Gregersen, JM Kane, ...
Genome biology 13 (1), 1-16, 2012
Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population
P Pal, M Mihanović, S Molnar, H Xi, G Sun, S Guha, N Jeran, ...
Croatian medical journal 50 (4), 361-369, 2009
Development of novel heminested PCR assays based on mitochondrial 16s rRNA gene for identification of seven pecora species
S Guha, VK Kashyap
BMC genetics 6 (1), 1-7, 2005
Consensus interpretation of the p. Met34Thr and p. Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel
J Shen, AM Oza, I Del Castillo, H Duzkale, T Matsunaga, A Pandya, ...
Genetics in Medicine 21 (11), 2442-2452, 2019
Molecular identification of lizard by RAPD & FINS of mitochondrial 16s rRNA gene
S Guha, VK Kashyap
Legal Medicine 8 (1), 5-10, 2006
Concordance study on 15 STR loci in three major populations of Himalayan state Sikkim
VK Kashyap, S Guha, R Trivedi
Journal of Forensic Science 47 (5), 1-5, 2002
Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation
OH Rinella ES, Shao Y, Yackowski L, Pramanik S, Oratz
Human Genetics, 2013
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