Subrata Kumar Dey

Targeted Next Generation Sequencing Revealed a Novel Homozygous Loss-of-Function Mutation in ILDR1 Gene Causes Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in a Chinese Family

Jinxia An, Jie Yang, Yan Wang et al. · Frontiers in Genetics · 2019 · 432 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations

Sujay Ghosh, Eleanor Feingold, Subrata Kumar Dey · American Journal of Medical Genetics Part A · 2009 · 212 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification and functional characterization of mutations in <i>LPL</i> gene causing severe hypertriglyceridaemia and acute pancreatitis

Peng Han, Guohong Wei, Ke Cai et al. · Journal of Cellular and Molecular Medicine · 2020 · 104 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole exome sequencing identified a homozygous novel variant in <i>CEP290</i> gene causes Meckel syndrome

Rui Zhang, Shaoyun Chen, Peng Han et al. · Journal of Cellular and Molecular Medicine · 2019 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Ligating properties of a potentially tetradentate Schiff base [(CH3)2NCH2CH2NCHC6H3(OH)(OMe)] with zinc(ii), cadmium(ii), cobalt(ii), cobalt(iii) and manganese(iii) ions: synthesis and structural studies

Soma Sen, Pritha Talukder, Subrata Kumar Dey et al. · Dalton Transactions · 2006 · 74 citations

Natural Sciences, Biochemistry, Chemistry +17