Soma Das mainly investigates Internal medicine, Genetics, Genotype, Pharmacogenetics and Pharmacology. Her Risk factor study in the realm of Internal medicine connects with subjects such as Glucuronide. Her work in the fields of Genetics, such as Missense mutation, Mutation, Microcephaly and Genomic imprinting, intersects with other areas such as Epidermal growth factor.
Her Genotype research integrates issues from Germline mutation, Glucuronidation, Allele and Bioinformatics. Her study in Pharmacogenetics is interdisciplinary in nature, drawing from both Pharmacogenomics, Pharmacodynamics and Genetic testing. Her Medical genetics research includes elements of Postnatal microcephaly, Molecular pathology, Rett syndrome and Leiden Open Variation Database.
Soma Das focuses on Genetics, Internal medicine, Genotype, Gene and Molecular biology. Her work is connected to Missense mutation, Mutation, Lissencephaly, Exon and Genetic testing, as a part of Genetics. Soma Das combines subjects such as Endocrinology, Oncology, Gastroenterology, Pharmacogenetics and Pharmacology with her study of Internal medicine.
Her Pharmacokinetics study, which is part of a larger body of work in Pharmacology, is frequently linked to Glucuronide, bridging the gap between disciplines. Her work in the fields of Genotype, such as Polymorphism, overlaps with other areas such as Acute lymphocytic leukemia. Her work carried out in the field of Molecular biology brings together such families of science as Phenotype, Glucuronidation, Single-nucleotide polymorphism and Gene expression.
Her primary areas of study are Genetics, Internal medicine, Genetic testing, Ataxia and Germline. Her study in the field of Gene, Mutation and Lissencephaly is also linked to topics like Cohesin complex and SMC1A. Her Internal medicine research incorporates elements of Endocrinology, Nitrosamine Metabolism, Oncology and Pharmacology.
She interconnects Family medicine, Immunology, MEDLINE and Bioinformatics in the investigation of issues within Genetic testing. Her MEDLINE study incorporates themes from Leiden Open Variation Database, Guideline, Concordance and Acute leukemia. Her Medical genetics research incorporates themes from Data science and Sequence.
Her scientific interests lie mostly in MEDLINE, Bioinformatics, Exome, Internal medicine and Family medicine. In most of her MEDLINE studies, her work intersects topics such as Genetic testing. In her work, Immunology is strongly intertwined with Gene panel, which is a subfield of Genetic testing.
The Internal medicine study combines topics in areas such as UGT2B7, Glucuronidation, Endocrinology, Oncology and Pharmacology. Her Family medicine research is multidisciplinary, relying on both Leiden Open Variation Database, Sequence, Concordance and Medical genetics. The various areas that she examines in her Medical genetics study include Guideline and Molecular pathology.
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards;Nazneen Aziz;Nazneen Aziz;Sherri Bale;David Bick.
Genetics in Medicine (2015)
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan.
Federico Innocenti;Samir D. Undevia;Lalitha Iyer;Pei Xian Chen.
Journal of Clinical Oncology (2004)
UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity
L Iyer;S Das;L Janisch;M Wen.
Pharmacogenomics Journal (2002)
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
C Sue Richards;Sherri Bale;Daniel B Bellissimo;Soma Das.
Genetics in Medicine (2008)
Assuring the quality of next-generation sequencing in clinical laboratory practice
Amy S Gargis;Lisa Kalman;Meredith W Berry;David P Bick.
Nature Biotechnology (2012)
Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism
Lalitha Iyer;Diana Hall;Soma Das;Melissa A. Mortell.
Clinical Pharmacology & Therapeutics (1999)
PTEN methylation is associated with advanced stage and microsatellite instability in endometrial carcinoma.
Helga B. Salvesen;Helga B. Salvesen;Nicola MacDonald;Andy Ryan;Ian J. Jacobs.
International Journal of Cancer (2001)
Methylation-specific PCR simplifies imprinting analysis.
Takeo Kubota;Soma Das;Susan L. Christian;Stephen B. Baylin.
Nature Genetics (1997)
Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation
Mitsuhiro Kato;Soma Das;Kristin Petras;Kunio Kitamura.
Human Mutation (2004)
Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations
Katrina Tatton-Brown;Jenny Douglas;Kim Coleman;Geneviève Baujat.
American Journal of Human Genetics (2005)
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