Soma Das

43.8k citations

158 papers · 26.5k indexed · 4 hit papers · h-index 47

Impact in

Genetics top 0.02%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Molecular Biology top 0.2%

Papers in

Genetics 48
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 15
- Genetic Syndromes and Imprinting 9
Pediatrics, Perinatology and Child Health 31
- Neonatal Health and Biochemistry 12

Co-authors: Sherri J. Bale Wayne W. Grody Madhuri Hegde Elaine Lyon Heidi L. Rehm Sue Richards David Bick Karl V. Voelkerding
Journals: Blood (11 papers)Genetics in Medicine (9 papers)Journal of Clinical Oncology (7 papers)Clinical Genetics (5 papers)Human Mutation (5 papers)
Partner nations: United States India Canada

In The Last Decade

Soma Das

152 papers receiving 26.2k citations

Hit Papers

align trajectories log scale

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 2015 · 18.9k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2015 Genetics in Medicine
2008 Genetics in Medicine
2004 Journal of Clinical Oncology
2002 The Pharmacogenomics Journal

Peers

Countries citing papers authored by Soma Das

Since Specialization

Citations

This map shows the geographic impact of Soma Das's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Soma Das with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Soma Das more than expected).

Fields of papers citing papers by Soma Das

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Soma Das. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Soma Das. The network helps show where Soma Das may publish in the future.

Co-authors

The 25 scholars most cited alongside Soma Das, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Soma Das Line = papers co-authored together Soma Das links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The future of diabetes mellitus management: Therapeutic insights from gene and stem cell research Gene Reports ·Soma Das, David Sanders, K. Sreedhara Ranganath Pai	2025	0
2	Expedited evaluation of hereditary hematopoietic malignancies in the setting of stem cell transplantation Haematologica ·Gregory W. Roloff, Satyajit Kosuri, Canavaggia, Adam DuVall, Anand Patel, Peter A. Riedell, Olatoyosi Odenike, Wendy Stock, Richard A. Larson, Michael R. Bishop, Анна Олексієнко, Lucy A. Godley, T. Wang, Daniela del Gaudio, Soma Das, Cheng Lian, Michael W. Drazer	2024	1
3	Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies Blood Advances ·Caner Saygin, Gregory W. Roloff, Christopher N Hahn, Rakchha Chhetri, Saar Gill, Hany Elmariah, Chetasi Talati, Анна Олексієнко, Guimin Gao, Roja Rajasekaran, Michael R. Bishop, Satyajit Kosuri, Soma Das, Deepak Singhal, Parvathy Venugopal, Claire C. Homan, Anna Brown, Hamish S. Scott, Devendra Hiwase, Lucy A. Godley	2022	23
4	Prevalence of RFC1 -mediated spinocerebellar ataxia in a North American ataxia cohort Neurology Genetics ·Zhaoheng Lv, Darice Y. Wong, Impulzus-Üzemű Ambrus, Claudio M. de Gusmão, Sinarianda Kurnia Hartantien, May Sanyoura, M Warchalowski, Paul J. Lockhart, Sharon Hassin‐Baer, Vikram Khurana, Christopher M. Gómez, Susan Perlman, Soma Das, Brent L. Fogel	2020	32
5	Prevalence of RFC1-Mediated Spinocerebellar Ataxia in a North American Ataxia Cohort Annals of Neurology ·Zhaoheng Lv, Darice Y. Wong, Impulzus-Üzemű Ambrus, Claudio M. de Gusmão, Sinarianda Kurnia Hartantien, May Sanyoura, M Warchalowski, Paul J. Lockhart, Sharon Hassin‐Baer, Vikram Khurana, Christopher M. Gómez, Susan Perlman, Soma Das, Brent L. Fogel	2020	3
6	Reduced edge‐to‐edge spaced MIMO antenna using parallel coupled line resonator for WLAN applications Microwave and Optical Technology Letters ·K. L. Rangaiah Setty, Gertrude Abbo, Kaushik Mandal, Soma Das	2019	13
7	Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation SHILAP Revista de lepidopterología ·Erin Conboy, Filippo Pinto e Vairo, Darrel Waggoner, Carole Ober, Soma Das, Radhika Dhamija, Eric W. Klee, Pavel N. Pichurin	2017	13
8	Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar Genetics in Medicine ·Steven M. Harrison, Jill S. Dolinsky, Amy E. Knight Johnson, Tina Pesaran, Danielle R. Azzariti, Sherri J. Bale, Elizabeth Chao, Soma Das, Lisa M. Vincent, Heidi L. Rehm	2017	145
9	Ultrafast Relaxation Dynamics of Luminescent Copper Nanoclusters (Cu₇L₃) and Efficient Electron Transfer to Functionalized Reduced Graphene Oxide The Journal of Physical Chemistry C ·Subarna Maity, Dipankar Bain, Kalishankar Bhattacharyya, Soma Das, Rajesh Bera, Bikash Jana, Bipattaran Paramanik, Ayan Datta, Amitava Patra	2017	46
10	Assessment of genetic diversity among Sargassum species from selected locations along the north-west coast of India Indian Journal of Fisheries ·Soma Das, Aparna Chaudhari, Geetanjali Deshmukhe, P. Gireesh Babu	2015	3
11	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 Genetics in Medicine ·Sue Richards, Nazneen Aziz, Sherri J. Bale, David Bick, Soma Das, Julie M. Gastier‐Foster, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector, Karl V. Voelkerding, Heidi L. Rehm Hit paper breakdown →	2015	18892
12	UGT1A and UGT2B Genetic Variation Alters Nicotine and Nitrosamine Glucuronidation in European and African American Smokers Cancer Epidemiology Biomarkers & Prevention ·Catherine A. Wassenaar, David V. Conti, Soma Das, Peixian Chen, Edwin H. Cook, Mark J. Ratain, Neal L. Benowitz, Rachel F. Tyndale	2014	25
13	The first case of CDK5RAP2-related primary microcephaly in a non-consanguineous patient identified by next generation sequencing Brain and Development ·Christopher Tan, Scott Topper, Heitor Yuri Nogara, Jennifer Stein, IN Mavridis, Kelly Arndt, Soma Das	2013	25
14	Novel Functional Germline Variants in the VEGF Receptor 2 Gene and Their Effect on Gene Expression and Microvessel Density in Lung Cancer Clinical Cancer Research ·Dylan M. Glubb, Elisa Cerri, Dumitru SPERMEZAN, Wei Zhang, Osman Mirza, Emma E. Thompson, Peixian Chen, Soma Das, Jacek Jassem, Witold Rzyman, Mark W. Lingen, Ravi Salgia, Fred R. Hirsch, Rafał Dziadziuszko, Kurt Ballmer‐Hofer, Federico Innocenti	2011	65
15	Genetic Variants Contributing to Daunorubicin-Induced Cytotoxicity Cancer Research ·R. Stephanie Huang, Shiwei Duan, Emily O. Kistner, Wasim K. Bleibel, Shannon M. Delaney, Donna L. Fackenthal, Soma Das, M. Eileen Dolan	2008	54
16	Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia European Journal of Human Genetics ·Eden Haverfield, R. A. QUERINO, Kristin Petras, William B. Dobyns, Soma Das	2008	51
17	Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance American Journal of Medical Genetics Part A ·Małgorzata J.M. Nowaczyk, Melissa T. Carter, Jie Xu, Marlene J. Huggins, Gordana Raca, Soma Das, Christa Lese Martin, Stuart Schwartz, Robert L. Rosenfield, Darrel Waggoner	2008	20
18	Global gene expression as a function of germline genetic variation Human Molecular Genetics ·Deborah French, Mark R. Wilkinson, Wenjian Yang, Luc de Chaisemartin, Edwin H. Cook, Soma Das, Mark J. Ratain, William E. Evans, James R. Downing, Ching‐Hon Pui, Mary V. Relling	2005	13
19	Haplotypes of variants in the UDP-glucuronosyltransferase1A9 and 1A1 genes Pharmacogenetics and Genomics ·Federico Innocenti, Wanqing Liu, Peixian Chen, Apurva A. Desai, Soma Das, Mark J. Ratain	2005	90
20	Methylation Analysis of the Fragile X Syndrome by PCR Genetic Testing ·Soma Das, Takeo Kubota, Min‐Ae Song, Richard A. Daniel, Elizabeth Berry‐Kravis, T. Prior, Bradley W. Popovich, W.G. Baxter, Tadao Arinami, David H. Ledbetter	1997	36

About Soma Das

Soma Das is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Hematology and Oncology, having authored 158 papers that have together received 26.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (16 papers), Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (15 papers), Neonatal Health and Biochemistry (12 papers), Cancer therapeutics and mechanisms (12 papers), Acute Lymphoblastic Leukemia research (12 papers), DNA Repair Mechanisms (10 papers) and Genetic Syndromes and Imprinting (9 papers). The work is most often cited by research in Genetics (10.5k citations), Molecular Biology (12.7k citations), Clinical Biochemistry (1.1k citations), Genetics (1.7k citations) and Cancer Research (2.3k citations). Soma Das has collaborated with scholars based in United States, India and Canada. Frequent co-authors include Sherri J. Bale, Wayne W. Grody, Madhuri Hegde, Elaine Lyon, Heidi L. Rehm, Sue Richards, David Bick, Karl V. Voelkerding, Julie M. Gastier‐Foster and Nazneen Aziz. Their work appears in journals such as Blood, Genetics in Medicine, Journal of Clinical Oncology, Clinical Genetics and Human Mutation.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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