Chris Cotsapas

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

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 15 papers. Top paper: “Survey of variation in human transcription factors reveals prevalent DNA binding changes”.

Survey of variation in human transcription factors reveals prevalent DNA binding changes

Science(2016)10.1126/science.aad2257

N/A

4.7DataRank · unranked

153 citations

Anastasia Vedenko, Jesse V. Kurland, Julia M. Rogers, Stephen S. Gisselbrecht, Elizabeth J. Rossin +19 more

Locus for severity implicates CNS resilience in progression of multiple sclerosis

Nature(2023)10.1038/s41586-023-06250-x

N/A

3.3DataRank · unranked

236 citations

Pernilla Stridh, Jacob L. McCauley, Janna Saarela, Aletta M.R. van den Bosch, Hendrik J. Engelenburg +95 more

The missing link between genetic association and regulatory function

eLife(2022)10.7554/elife.74970

N/A

3.1DataRank · unranked

160 citations

Sumaiya Nazeen, Daniel Lee, Huwenbo Shi, J Stamatoyannopoulos, Sung Chun +4 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits

PLoS Genetics(2022)10.1371/journal.pgen.1010557

N/A

0.434DataRank · unranked

17 citations

Sebastian Akle, Athanasios Teodosiadis, Brian E. Cade, Heming Wang, Tamar Sofer +13 more

Joint analysis reveals shared autoimmune disease associations and identifies common mechanisms

medRxiv(2021)10.1101/2021.05.13.21257044

N/A

0DataRank · unranked

13 citations

Noah J Connally, Pierre‐Paul Axisa, Christiane Gasperi, Mitja Mitrovič, David A. van Heel +13 more

Genetics of multiple sclerosis: lessons from polygenicity

The Lancet Neurology(2022)10.1016/s1474-4422(22)00255-1

N/A

0DataRank · unranked

106 citations

Marijne Vandebergh, Jacob L. McCauley, Janna Saarela, Chris Cotsapas, An Goris

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Nature Neuroscience(2024)10.1038/s41593-024-01747-8

N/A

0DataRank · unranked

58 citations

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori +95 more

Genome-wide association meta-analyses of drug-resistant epilepsy

EBioMedicine(2025)10.1016/j.ebiom.2025.105675

N/A

0DataRank · unranked

12 citations

Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed +88 more

MICBG406A polymorphism reduces risk of mechanical ventilation and death during viral acute lung injury

JCI Insight(2025)10.1172/jci.insight.191951

N/A

0DataRank · unranked

1 citations

Narges Alipanah, Ernie Chen, Dylan Duchen, Holden T. Maecker, Seunghee Kim‐Schulze +49 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406

N/A

0DataRank · unranked

1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Brain(2020)10.1093/brain/awaa171

N/A

0DataRank · unranked

81 citations

Eduardo Pérez‐Palma, Daniel P. Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus +86 more

Epilepsy risk in offspring of affected parents; a cohort study of the “maternal effect” in epilepsy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51258

N/A

0DataRank · unranked

21 citations

Colin A. Ellis, Samuel F. Berkovic, Chris Cotsapas, Ruth Ottman, Jakob Christensen +1 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

The missing link between genetic association and regulatory function

medRxiv(2021)10.1101/2021.06.08.21258515

N/A

0DataRank · unranked

19 citations

Sumaiya Nazeen, Daniel Lee, Huwenbo Shi, J Stamatoyannopoulos, Sung Chun +4 more