Craig Smail

Also affiliated with Mercy Research

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 14 papers. Top paper: “Transcriptomic signatures across human tissues identify functional rare genetic variation”.

Transcriptomic signatures across human tissues identify functional rare genetic variation

Science(2020)10.1126/science.aaz5900

N/A

5.0DataRank · unranked

166 citations

Benjamin J. Strober, Jonah Einson, Nathan S. Abell, François Aguet, Alvaro N. Barbeira +183 more

Discovery and quality analysis of a comprehensive set of structural variants and short tandem repeats

Nature Communications(2020)10.1038/s41467-020-16481-5

N/A

1.2DataRank · unranked

38 citations

Erin N. Smith, Matteo D’Antonio, Marc Jan Bonder, William W. Greenwald, Agnieszka D’Antonio‐Chronowska +14 more

Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease

Cell(2021)10.1016/j.cell.2021.03.050

N/A

0.804DataRank · unranked

212 citations

Daniel C. Nachun, Nicole M. Ferraro, Michael J. Gloudemans, Abhiram S. Rao, Craig Smail +168 more

Properties of structural variants and short tandem repeats associated with gene expression and complex traits

Nature Communications(2020)10.1038/s41467-020-16482-4

N/A

0.741DataRank · unranked

139 citations

Matteo D’Antonio, Marc Jan Bonder, Craig Smail, Margaret K. R. Donovan, William W. Greenwald +15 more

Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics

Nature Genetics(2021)10.1038/s41588-021-00800-7

N/A

0.650DataRank · unranked

75 citations

Craig Smail, Michael J. Gloudemans, Laure Frésard, David Jakubosky, Matteo D’Antonio +22 more

Integration of rare expression outlier-associated variants improves polygenic risk prediction

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.015

N/A

0.524DataRank · unranked

32 citations

Nicole M. Ferraro, Qin Hui, Matthew G. Durrant, Matthew Aguirre, Yosuke Tanigawa +14 more

Integration of rare large-effect expression variants improves polygenic risk prediction

medRxiv(2020)10.1101/2020.12.02.20242990

N/A

0.241DataRank · unranked

4 citations

Nicole M. Ferraro, Matthew G. Durrant, Abhiram Rao, Matthew Aguirre, Xin Li +12 more

Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores

medRxiv(2024)10.1101/2024.03.15.24304216

N/A

0DataRank · unranked

0 citations

Carl Schwendinger-Schreck, Bing Ge, Warren Cheung, Rebecca McLennan, Jeffrey Johnston +3 more

Nonsense-mediated decay is highly stable across individuals and tissues

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.008

N/A

0DataRank · unranked

44 citations

Daniel Nachun, Tiffany Y. Eulalio, Nicole M. Ferraro, Craig Smail, Manuel A. Rivas +2 more

Nonsense-mediated decay is highly stable across individuals and tissues

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.03.429654

N/A

0DataRank · unranked

6 citations

Daniel Nachun, Tiffany Y. Eulalio, Nicole M. Ferraro, Craig Smail, Manuel A. Rivas +2 more

Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape

Nature Communications(2023)10.1038/s41467-023-40424-5

N/A

0DataRank · unranked

57 citations

Esteban M. Domínguez, Boryana Koseva, Joseph M. Varberg, Ross McNally, Ayelen Moreno‐Irusta +13 more

RNA Sequencing in Disease Diagnosis

Annual Review of Genomics and Human Genetics(2024)10.1146/annurev-genom-021623-121812

N/A

0DataRank · unranked

29 citations

Stephen B. Montgomery, Craig Smail

Complex trait associations in rare diseases and impacts on Mendelian variant interpretation

Nature Communications(2024)10.1038/s41467-024-52407-1

N/A

0DataRank · unranked

9 citations

Bing Ge, Marissa R. Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey Johnston +8 more

Complex trait associations in rare diseases and impacts on Mendelian variant interpretation

medRxiv(2024)10.1101/2024.01.10.24301111

N/A

0DataRank · unranked

3 citations

Bing Ge, Marissa R. Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey Johnston +8 more