List of works - Saurav Guha

A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis

scientific article published on 11 May 2011

Association of ApoE genetic variants with obstructive sleep apnea in children.

scientific article published on 19 July 2007

Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

scientific article published on August 2009

Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry.

scientific article published in October 2009

Correlation analyses reveal a substantial influence of allelic gaps on the investigation of genetic diversity of modern human populations with microsatellites

scientific article published on 29 April 2008

De novo copy number variants are associated with congenital diaphragmatic hernia

scientific article published on October 2012

Development of novel heminested PCR assays based on mitochondrial 16s rRNA gene for identification of seven pecora species

scientific article

Genetic architecture of prostate cancer in the Ashkenazi Jewish population

scientific article

Genetic structure of Indian populations based on fifteen autosomal microsatellite loci

scientific article

Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation

scientific article

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

scientific article published on January 2013

Genomic variation in the mitochondrially encoded cytochrome b (MT-CYB) and 16S rRNA (MT-RNR2) genes: characterization of eight endangered Pecoran species

scientific article published on 01 June 2006

High rate of disease-related copy number variations in childhood onset schizophrenia.

scientific article published on 21 May 2013

Implication of a rare deletion at distal 16p11.2 in schizophrenia

scientific article published on March 2013

Implications for health and disease in the genetic signature of the Ashkenazi Jewish population

scientific article

Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).

scientific article published on 17 December 2013

Molecular identification of lizard by RAPD & FINS of mitochondrial 16s rRNA gene.

scientific article

Novel splice mutation in microthalmia-associated transcription factor in Waardenburg Syndrome.

scientific article published on 27 March 2011

Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin

scientific article published on 26 June 2007

List of works by Saurav Guha

A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis

Association of ApoE genetic variants with obstructive sleep apnea in children.

Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry.

Correlation analyses reveal a substantial influence of allelic gaps on the investigation of genetic diversity of modern human populations with microsatellites

De novo copy number variants are associated with congenital diaphragmatic hernia

Development of novel heminested PCR assays based on mitochondrial 16s rRNA gene for identification of seven pecora species

Genetic architecture of prostate cancer in the Ashkenazi Jewish population

Genetic structure of Indian populations based on fifteen autosomal microsatellite loci

Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

Genomic variation in the mitochondrially encoded cytochrome b (MT-CYB) and 16S rRNA (MT-RNR2) genes: characterization of eight endangered Pecoran species

High rate of disease-related copy number variations in childhood onset schizophrenia.

Implication of a rare deletion at distal 16p11.2 in schizophrenia

Implications for health and disease in the genetic signature of the Ashkenazi Jewish population

Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).

Molecular identification of lizard by RAPD & FINS of mitochondrial 16s rRNA gene.

Novel splice mutation in microthalmia-associated transcription factor in Waardenburg Syndrome.

Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin