K. Darvishi

发表

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

Joshua M. Korn, Marcia M. Nizzari, S. Gabriel, 2008, Nature Genetics.

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

Ryan E. Mills, H. P. Kang, O. Gokcumen, 2010, Nature Genetics.

Integrating common and rare genetic variation in diverse human populations

Sharon R Grossman, Pardis C Sabeti, P. Deloukas, 2010, Nature.

Association study of major risk single nucleotide polymorphisms in the common regulatory region of PARK2 and PACRG genes with leprosy in an Indian population

D. Malhotra, K. Darvishi, H. Kumar, 2006, European Journal of Human Genetics.

Implication of BRCA2 -26G>A 5' untranslated region polymorphism in susceptibility to sporadic breast cancer and its modulation by p53 codon 72 Arg>Pro polymorphism

K. Darvishi, S. Husain, M. Raish, 2007, Breast Cancer Research.

The Indian origin of paternal haplogroup R1a1* substantiates the autochthonous origin of Brahmins and the caste system

K. Darvishi, A. Bhat, P. Tiwari, 2009, Journal of Human Genetics.

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

Ryan Mills, Ji Hyeon Park, Aparna Prasad, 2011, Nature Biotechnology.

The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol[S]

Magalie S Leduc, S. Kathiresan, M. Orho-Melander, 2011, Journal of Lipid Research.

Application of Nexus Copy Number Software for CNV Detection and Analysis

K. Darvishi, 2010, Current protocols in human genetics.

Copy number variation prevalence in known asthma genes and their impact on asthma susceptibility

Ryan E. Mills, Charles Lee, R. Mills, 2013, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Copy number variation genotyping using family information

Ryan Mills, Iuliana Ionita-Laza, Charles Lee, 2013, BMC Bioinformatics.

Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.

K. Darvishi, A. Bhat, R. Bamezai, 2007, Cancer letters.

Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia

K. Lage, P. Donahoe, A. Kashani, 2015, Clinical genetics.

Integrating common and rare genetic variation in diverse human populations

Joshua M. Korn, Pardis C Sabeti, P. Deloukas, 2010, Nature.

Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia

K. Darvishi, B. Pober, M. Loscertales, 2015, Clinical genetics.