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Journal of Human Genetics|December 23, 2006
Hereditary prosopagnosia (HPA): the first report outside the Caucasian populationIngo Kennerknecht, Nina Plümpe, Steve Edwards, et al.Plos One|August 13, 2013
Low birthweight (LBW) and neonatal hyperbilirubinemia (NNH) in an Indian cohort: association of homocysteine, its metabolic pathway genes and micronutrients as risk factorsKrishna Kishore Sukla, Pankaj Kumar Tiwari, Ashok Kumar, et al.International Journal of Andrology|April 7, 2005
Mutation C677T in the methylenetetrahydrofolate reductase gene is associated with male infertility in an Indian populationKiran Singh, S K Singh, R Sah, et al.European Journal of Pediatrics|July 24, 2013
Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newbornsPankaj Kumar Tiwari, Amanpreet Sethi, Sriparna Basu, et al.Journal of Genetics|April 19, 2018
Genetic heterogeneity in Van der Woude syndrome: identification of NOL4 and IRF6 haplotype from the noncoding region as candidates in two familiesPriyanka Kumari Kumari, Akhtar Ali, Subodh Kumar Singh, et al.Journal of the Indian Medical Association|February 2, 2008
Hepatocellular carcinoma presenting as neutrophilic leukaemoid reaction--a rare entityVijai Tilak, Madhukar Rai, V P Singh, et al.Journal of Biosciences|February 7, 2013
Lower incidence of nonsyndromic cleft lip with or without cleft palate in females: is homocysteine a factor?Priyanka Kumari, Akhtar Ali, Krishna K Sukla, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 26, 2010
Mutational analysis of the androgen receptor gene in two Indian families with partial androgen insensitivity syndromeM R Nagaraja, Amit Rastogi, Rajiva Raman, et al.Journal of Human Genetics|February 21, 2006
MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothersAmit Kumar Rai, Satya Singh, Stuti Mehta, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|June 30, 2010
Molecular diagnosis of 46,XY DSD and identification of a novel 8 nucleotide deletion in exon 1 of the SRD5A2 geneM R Nagaraja, Amit Rastogi, Rajiva Raman, et al.Pageof 4