Synthesis of carbon nanosheet from barley and its use as non-enzymatic glucose biosensor

Por Das, Soma, Saha, Mitali
Publicado no J Pharm Anal (2014)

Real-world evidence of glycemic control among patients with type 2 diabetes mellitus in India: the TIGHT study

Por Borgharkar, Surendra S, Das, Soma S
Publicado no BMJ Open Diabetes Res Care (2019)

Exome Sequencing and the Genetics of Intellectual Disability

Por Topper, Scott, Ober, Carole, Das, Soma
Publicado no Clin Genet (2011)

Panthotenate Kinase‐Associated Neurodegeneration Has a Founder Mutation (c.215_216insa) in Indian Agrawal Patients

Por Udani, Vrajesh, Das, Soma, Chhabria, Rahul
Publicado no Mov Disord Clin Pract (2016)

Best practices sharing: Setting up a professional clinical research unit in India

Por Divate, Uma, Das, Soma, Bhosale, Neelambari, Divate, Pathik
Publicado em 2014

Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia

Por Haverfield, Eden V, Whited, Amanda J, Petras, Kristin S, Dobyns, William B, Das, Soma
Publicado em 2009

A novel intronic mutation in MTM1 detected by RNA analysis in a case of X-linked myotubular myopathy

Por Al-Hashim, Aqeela, Gonorazky, Hernan D., Amburgey, Kimberly, Das, Soma, Dowling, James J.
Publicado no Neurol Genet (2017)

THGS: a web-based database of Transmembrane Helices in Genome Sequences

Por Fernando, S. A., Selvarani, P., Das, Soma, Kumar, Ch. Kiran, Mondal, Sukanta, Ramakumar, S., Sekar, K.
Publicado em 2004

Mandibuloacral Dysplasia Caused by LMNA Mutations and Uniparental Disomy

Por Bai, Shaochun, Lozada, Anthony, Jones, Marilyn C., Dietz, Harry C., Dempsey, Melissa, Das, Soma
Publicado em 2014

Water-Soluble Derivatives of Octanuclear Iron-Oxo-Pyrazolato Complexes; An Experimental and Computational Study

Por Das, Soma, Chakraborty, Indranil, Skachkov, Dmitry, Ahmadi, Majid, Ishikawa, Yasuyuki, Baran, Peter, Raptis, Raphael G.
Publicado em 2012

Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX

Por Moey, Ching, Topper, Scott, Karn, Mary, Johnson, Amy Knight, Das, Soma, Vidaurre, Jorge, Shoubridge, Cheryl
Publicado no Eur J Hum Genet (2016)

Colposcopically Observed Vascular Changes in the Cervix in Relation to the Hormonal Levels and Menstrual Cycle

Por Joshi, Smita N., Das, Soma, Thakar, Madhuri, Sahasrabuddhe, Vikrant, Kumar, B. Kishore, Callahan, Marianne, Mauck, Christine
Publicado em 2008

Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation

Por Conboy, Erin, Vairo, Filippo, Waggoner, Darrel, Ober, Carole, Das, Soma, Dhamija, Radhika, Klee, Eric W., Pichurin, Pavel
Publicado no Case Rep Genet (2017)

Clinical utility gene card for: Centronuclear and myotubular myopathies

Por Biancalana, Valérie, Beggs, Alan H, Das, Soma, Jungbluth, Heinz, Kress, Wolfram, Nishino, Ichizo, North, Kathryn, Romero, Norma B, Laporte, Jocelyn
Publicado em 2012

The 1200 Patients Project: Creating A New Medical Model System for Clinical Implementation of Pharmacogenomics

Por O’Donnell, Peter H., Bush, Angela, Spitz, Jared, Danahey, Keith, Saner, Don, Das, Soma, Cox, Nancy J., Ratain, Mark J.
Publicado no Clin Pharmacol Ther (2012)

Neuro-Ophthalmologic and Electroretinographic Findings in Pantothenate Kinase-Associated Neurodegeneration (formerly Hallervorden-Spatz Syndrome)

Por Egan, Robert A., Weleber, Richard G., Hogarth, Penelope, Gregory, Allison, Coryell, Jason, Westaway, Shawn K., Gitschier, Jane, Das, Soma, Hayflick, Susan J.
Publicado em 2005

Genetic Variants Contributing to Daunorubicin-Induced Cytotoxicity

Por Huang, R. Stephanie, Duan, Shiwei, Kistner, Emily O., Bleibel, Wasim K., Delaney, Shannon M., Fackenthal, Donna L., Das, Soma, Dolan, M. Eileen
Publicado em 2008

Population-specific GSTM1 copy number variation

Por Huang, R. Stephanie, Chen, Peixian, Wisel, Steve, Duan, Shiwei, Zhang, Wei, Cook, Edwin H., Das, Soma, Cox, Nancy J., Dolan, M. Eileen
Publicado em 2009

UGT1A and UGT2B genetic variation alters nicotine and nitrosamine glucuronidation in European and African American smokers

Por Wassenaar, Catherine A., Conti, David V., Das, Soma, Chen, Peixian, Cook, Edwin H., Ratain, Mark J., Benowitz, Neal L., Tyndale, Rachel F.
Publicado no Cancer Epidemiol Biomarkers Prev (2014)

A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an ELOVL4 mutation

Por Xiao, Changrui, Binkley, Elaine M., Rexach, Jessica, Knight-Johnson, Amy, Khemani, Pravin, Fogel, Brent L., Das, Soma, Stone, Edwin M., Gomez, Christopher M.
Publicado no Neurol Genet (2019)