Craig Smail (C Smail)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 11

Top Topics

Dna Methylation

Respiratory Syncytial Virus

Autism Spectrum Disorder

Top Venues

medRxiv : the preprint server for health sciences

Nature genetics

Nature communications

This page only lists publications with an associated author ORCID identifier.

Publications

Craig Smail, Bing Ge, Marissa R Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey J Johnston, Cassandra Barrett, null null, Keith Feldman, Ana S A Cohen, Emily G Farrow, Isabelle Thiffault, Elin Grundberg, Tomi Pastinen
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation. medRxiv : the preprint server for health sciences (2024)
Craig Smail, Bing Ge, Marissa R Keever-Keigher, Carl Schwendinger-Schreck, Warren A Cheung, Jeffrey J Johnston, Cassandra Barrett, null null, Keith Feldman, Christiane Zweier, Emily G Farrow, Isabelle Thiffault, Elin Grundberg, Tomi Pastinen
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation. Nature communications 15 (1) (2024)
Craig Smail, Bing Ge, Marissa R Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey J Johnston, Cassandra Barrett, null null, Keith Feldman, Ana S A Cohen, Emily G Farrow, Isabelle Thiffault, Elin Grundberg, Tomi Pastinen
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation. medRxiv : the preprint server for health sciences (2024)
Cas LeMaster, Carl Schwendinger-Schreck, Bing Ge, Warren A Cheung, Rebecca McLennan, Jeffrey J Johnston, Tomi Pastinen, Craig Smail
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv : the preprint server for health sciences (2024)
Cas LeMaster, Carl Schwendinger-Schreck, Bing Ge, Warren Cheung, Rebecca McLennan, Jeffrey Johnston, Tomi Pastinen, Craig Smail
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv : the preprint server for health sciences (2024)
Cas LeMaster, C Schwendinger-Schreck, B Ge, W Cheung, J J Johnston, T Pastinen, Craig Smail
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv : the preprint server for health sciences (2024)
Craig Smail, Bing Ge, Marissa R Keever-Keigher, Carl Schwendinger-Schreck, Warren Cheung, Jeffrey J Johnston, Cassandra Barrett, null null, Keith Feldman, Ana S A Cohen, Emily G Farrow, Isabelle Thiffault, Elin Grundberg, Tomi Pastinen
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation. medRxiv : the preprint server for health sciences (2024)
Cas LeMaster, C Schwendinger-Schreck, B Ge, W Cheung, J J Johnston, T Pastinen, Craig Smail
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv : the preprint server for health sciences (2024)
Cas LeMaster, Carl Schwendinger-Schreck, Bing Ge, Warren Cheung, Rebecca McLennan, Jeffrey Johnston, Tomi Pastinen, Craig Smail
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv : the preprint server for health sciences (2024)
Cas LeMaster, C Schwendinger-Schreck, B Ge, W Cheung, J J Johnston, T Pastinen, Craig Smail
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores. medRxiv : the preprint server for health sciences (2024)
Marc Jan Bonder, Craig Smail, Michael J Gloudemans, Laure Frésard, David Jakubosky, Matteo D'Antonio, Xin Li, Nicole M Ferraro, Ivan Carcamo-Orive, Bogdan Mirauta, Daniel D Seaton, Na Cai, Dara Vakili, Danilo Horta, Chunli Zhao, Diane B Zastrow, Devon E Bonner, null null, null null, null null, null null, Matthew T Wheeler, Helena Kilpinen, Joshua W Knowles, Erin N Smith, Kelly A Frazer, Stephen B Montgomery, Oliver Stegle
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Nature genetics 53 (3) (2021)