Shamika Ketkar

Also affiliated with Texas Children's Hospital, Children's Cancer Center

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 23 papers. Top paper: “Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing”.

Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing

Journal of Clinical Investigation(2020)10.1172/jci141500

N/A

0DataRank · unranked

189 citations

Hongzheng Dai, Lindsay C. Burrage, Jill A. Rosenfeld, Shamika Ketkar, Michaela Müller +13 more

The safety and clinical effects of administering a multiantigen-targeted T cell therapy to patients with multiple myeloma

Science Translational Medicine(2020)10.1126/scitranslmed.aaz3339

N/A

0DataRank · unranked

40 citations

Ifigeneia Tzannou, Spyridoula Vasileiou, George Carrum, Carlos A. Ramos, Rammurti T. Kamble +19 more

Leukocyte-dependent effects of platelet-rich plasma on cartilage loss and thermal hyperalgesia in a mouse model of post-traumatic osteoarthritis

Osteoarthritis and Cartilage(2020)10.1016/j.joca.2020.06.004

N/A

0DataRank · unranked

37 citations

C. Liu, Brian Dawson, Shamika Ketkar, Shiv Patel, B.H. Lee +2 more

Tumor suppressor function of WT1 in acute promyelocytic leukemia

Haematologica(2021)10.3324/haematol.2021.279601

N/A

0DataRank · unranked

7 citations

Casey Katerndahl, Hayley R. LeBlanc, Tyler T. Elmendorf, Vaishali Basu, Margery Gang +9 more

RNA Sequencing as a Diagnostic Tool

JAMA(2022)10.1001/jama.2022.22843

N/A

0DataRank · unranked

35 citations

Lindsay C. Burrage, Brendan Lee, Shamika Ketkar

A novel, de novo intronic variant in POGZ causes White–Sutton syndrome

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62747

N/A

0DataRank · unranked

9 citations

David R. Murdock, Jill A. Rosenfeld, Hongzheng Dai, Shamika Ketkar, Lisa Emrick +10 more

Somatic Dnmt3a inactivation leads to slow, canonical DNA methylation loss in murine hematopoietic cells

iScience(2022)10.1016/j.isci.2022.104004

N/A

0DataRank · unranked

3 citations

Angela M. Verdoni, Haley Abel, David Y. Chen, Shamika Ketkar, Elizabeth R. Leight +3 more

Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature

medRxiv(2023)10.1101/2023.10.11.23296741

N/A

0DataRank · unranked

1 citations

Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie Russ-Hall, Amy Schneider +48 more

The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.007

N/A

0DataRank · unranked

28 citations

Sen Zhao, Jefferson C. Sinson, Aleksandar Bajić, Jill A. Rosenfeld, Matthew B. Neeley +23 more

Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement

Nature Communications(2024)10.1038/s41467-024-50159-6

N/A

0DataRank · unranked

24 citations

Cassandra Rastin, Soham Sengupta, Helen E. Pennington, Sophie Russ-Hall, Amy Schneider +50 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

N/A

0DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Dose-dependent effects of Dnmt3a in an inducible murine model of Kras-driven leukemia

Experimental Hematology(2024)10.1016/j.exphem.2024.104248

N/A

0DataRank · unranked

1 citations

Allison B. Rosen, Jaime M. Reyes, Shamika Ketkar, Shannon E. Conneely, Rohit Gupta +8 more

Development and evaluation of a training curriculum to engage researchers on accessing and analyzing the All of Us data

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae240

N/A

0DataRank · unranked

3 citations

Jasmine N Baker, Shamika Ketkar, Ashley M. Butler, LaTerrica Williams, Latanya Hammonds-Odie +5 more

Experiences in providing a community educational resource for the All of Us Researcher Workbench

Journal of the American Medical Informatics Association(2024)10.1093/jamia/ocae226

N/A

0DataRank · unranked

2 citations

Jinyoung Byun, Jun Wang, Stephen Richards, Pamela N. Luna, LaTerrica Williams +11 more

Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing

Human Molecular Genetics(2024)10.1093/hmg/ddae105

N/A

0DataRank · unranked

1 citations

Shamika Ketkar, Taotao Tan, Elizabeth G. Atkinson, Lindsay C. Burrage, Kim C. Worley +6 more

Recessive loss‐of‐function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine–Lubinsky syndrome

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63845

N/A

0DataRank · unranked

1 citations

Undiagnosed Diseases Network, Lisa Emrick, Jill A. Rosenfeld, Shamika Ketkar, Lindsay C. Burrage +2 more

The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.013

N/A

0DataRank · unranked

3 citations

Jefferson C. Sinson, Shenglan Li, Jill A. Rosenfeld, Gladys Zapata, Kristina Macakova +15 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0DataRank · unranked

4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 more

Integrative exome sequencing and machine learning identify MICB and interferon pathway genes as contributors to SSc risk

Annals of the Rheumatic Diseases(2025)10.1016/j.ard.2025.05.009

N/A

0DataRank · unranked

1 citations

Hongzheng Dai, Lindsay C. Burrage, David R. Murdock, Brian Dawson, Marialbert Acosta‐Herrera +9 more

The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics

medRxiv(2025)10.1101/2025.01.28.25321295

N/A

0DataRank · unranked

1 citations

Jefferson Sinson, Shenglan Li, Jill A. Rosenfeld, Gladys Zapata, Kristina Macakova +16 more

C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder

Genetics in Medicine(2025)10.1016/j.gim.2025.101429

N/A

0DataRank · unranked

0 citations

Laura Mackay, Maria Blazo, Elizabeth Mizerik, Jozef Gécz, Renée Carroll +34 more

Implementing a training resource for large-scale genomic data analysis in the All of Us Researcher Workbench

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.018

N/A

0DataRank · unranked

0 citations

Erik Stricker, Julie Coleman, Shamika Ketkar, Taotao Tan, Ashley M. Butler +7 more