Christine Stevens

Biochemistry, Genetics and Molecular Biology

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 1%percentile

25.3Author DataRank

Indexed papers

7in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 7 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 35 papers — median percentile 94. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Cell(2020)10.1016/j.cell.2019.12.036

N/A

9.5DataRank · unranked

2470 citations

Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An +95 more

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Nature Genetics(2022)10.1038/s41588-022-01156-2

N/A

3.7DataRank · unranked

195 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu +95 more

A first update on mapping the human genetic architecture of COVID-19

Nature(2022)10.1038/s41586-022-04826-7

Top 6%

3.5DataRank

Top 6%176 citations

Leadership, Gita A. Pathak, Juha Karjalainen, Christine Stevens, Benjamin M. Neale +86 more

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0

N/A

2.8DataRank · unranked

151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 more

An open resource of structural variation for medical and population genetics

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/578674

Top 9%

2.2DataRank

Top 9%44 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +37 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis

Cell(2019)10.1016/j.cell.2019.06.029

N/A

1.1DataRank · unranked

1412 citations

Moshe Biton, Keri M. Sullivan, Grace Burgin, Daniel B. Graham, Rebecca H. Herbst +28 more

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature Genetics(2022)10.1038/s41588-022-01104-0

N/A

0.969DataRank · unranked

638 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +112 more

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature Genetics(2013)10.1038/ng.2543

N/A

0.862DataRank · unranked

313 citations

Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel +43 more

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature Neuroscience(2019)10.1038/s41593-019-0527-8

N/A

0.815DataRank · unranked

228 citations

F. Kyle Satterstrom, Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis +17 more

Whole exome sequencing analyses reveal gene–microbiota interactions in the context of IBD

Gut(2020)10.1136/gutjnl-2019-319706

N/A

0.604DataRank · unranked

55 citations

Arnau Vich Vila, Ranko Gaćeša, Valerie Collij, Christine Stevens, Jack Fu +17 more

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Cell Reports(2021)10.1016/j.celrep.2021.110020

N/A

0.581DataRank · unranked

47 citations

Jennifer Nguyen, Timothy D. Arthur, Hiroko Matsui, Agnieszka D’Antonio‐Chronowska, Kelly A. Frazer +85 more

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

10.1101/2021.12.20.21267194

N/A

0.538DataRank · unranked

35 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +60 more

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

medRxiv(2021)10.1101/2021.06.15.21258641

N/A

0.500DataRank · unranked

11 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, María T. Abreu +95 more

ASD and ADHD have a similar burden of rare protein-truncating variants

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/277707

N/A

0.434DataRank · unranked

17 citations

Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis, Christine Stevens +18 more

Serum urate and cardiovascular events in the DCCT/EDIC study

Scientific Reports(2021)10.1038/s41598-021-90785-4

N/A

0.421DataRank · unranked

7 citations

Barbara H. Braffett, Arpita Basu, Ionut Bebu, Samuel Dagogo‐Jack, Trevor J. Orchard +86 more

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.12.248526

N/A

0.385DataRank · unranked

12 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Industrialization drives convergent microbial and physiological shifts in the human metaorganism

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.20.683358

N/A

0.241DataRank · unranked

4 citations

Malte Rühlemann, Ana Paula Schaan, Yue Ma, Lucas Moitinho‐Silva, Eike Matthias Wacker +61 more

Cystic fibrosis risk variants confer protection against inflammatory bowel disease

medRxiv(2024)10.1101/2024.12.02.24318364

N/A

0.208DataRank · unranked

3 citations

Qian Zhang, Kai Yuan, Aleksejs Sazonovs, Christine Stevens, Laura Fachal +4 more

CR1 variants contribute to FSGS susceptibility across multiple populations

medRxiv(2023)10.1101/2023.11.20.23298462

N/A

0.165DataRank · unranked

2 citations

Zora Modrušan, Alexander A. Loboda, Jeffrey B. Kopp, Cheryl A. Winkler, Alexey Sergushichev +6 more

CHARR efficiently estimates contamination from DNA sequencing data

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.011

N/A

0DataRank · unranked

10 citations

Laura D. Gauthier, Timothy Poterba, Edoardo Giacopuzzi, Julia K. Goodrich, Christine Stevens +5 more

zCall: a rare variant caller for array-based genotyping

UNC Libraries(2020)10.17615/2r6r-p404

N/A

0DataRank · unranked

0 citations

George Grant, Jared Maguire, Shaun Purcell, Jennifer L. Moran, Christine Stevens +12 more

Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.001

N/A

0DataRank · unranked

44 citations

Sini Nagpal, Suresh Venkateswaran, David J. Cutler, David T. Okou, Talin Haritunians +53 more

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.07.010

N/A

0DataRank · unranked

54 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Prevalence and Effect of Genetic Risk of Thromboembolic Disease in Inflammatory Bowel Disease

Gastroenterology(2020)10.1053/j.gastro.2020.10.019

N/A

0DataRank · unranked

16 citations

Gregory J. Botwin, Talin Haritunians, Dalin Li, Shaohong Yang, Michelle Khrom +14 more

CHARR efficiently estimates contamination from DNA sequencing data

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.28.545801

N/A

0DataRank · unranked

3 citations

Laura D. Gauthier, Timothy Poterba, Edoardo Giacopuzzi, Julia K. Goodrich, Christine Stevens +5 more

Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.03.587209

N/A

0DataRank · unranked

17 citations

Jonna Grimsby, Daniel P. Howrigan, Kai Yuan, Sinéad B. Chapman, Christine Stevens +12 more

Mapping and characterization of structural variation in 17,795 human genomes

UNC Libraries(2024)10.17615/bjv3-ys88

Top 100%

0DataRank

Top 100%0 citations

S.S. Rich, Elizabeth L. Appelbaum, Ryan M. Layer, Subra Kugathasan, Scott M. Damrauer +95 more

CR1 variants contribute to FSGS susceptibility across multiple populations

iScience(2025)10.1016/j.isci.2025.112234

N/A

0DataRank · unranked

2 citations

Zora Modrušan, Alexander A. Loboda, Jeffrey B. Kopp, Cheryl A. Winkler, Alexey Sergushichev +6 more

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

medRxiv(2025)10.1101/2024.12.27.24319460

N/A

0DataRank · unranked

3 citations

Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura G Sloofman +49 more

Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases

medRxiv(2025)10.1101/2025.07.11.25331388

N/A

0DataRank · unranked

0 citations

Jean‐Christophe Grenier, Justin Pelletier, Gabrielle Boucher, Geneviève Gagnon, Philippe Goyette +13 more

Christine Stevens

Indexed papers

Top data-sharing exemplar

Papers