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Paper Details

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
49
2018
ASPA, Asn409Ser, CD, Canavan disease, ClinVar alleles, Crohn's and rare diseases, Crohn's disease, ExAC, GBA, Gaucher disease, Glu285Ala, HEXA, LRRK2, Mendelian disease, NOD2, Tay-Sachs disease, Tyr427IlefsTer5, alleles, broadinstitute, c.1421, enriched alleles, p, protein-altering alleles, protein-coding alleles, rare alleles, rare diseases
Author NameAffiliation
Manuel A RivasBroad Institute
Manuel A RivasStanford University
Manuel A RivasBroad Institute
Manuel A RivasStanford University
Hailiang HuangBroad Institute
Hailiang HuangMassachusetts General Hospital
Christine StevensBroad Institute
Matti PirinenInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Matti PirinenUniversity of Helsinki
Talin HarituniansF. Widjaja Foundation Inflammatory Bowel and Immunobiology Research Institute, Cedars-Sinai Medical Center
Benjamin M NealeBroad Institute
Benjamin M NealeMassachusetts General Hospital
Benjamin M NealeBroad Institute
Benjamin M NealeMassachusetts General Hospital
Mitja I KurkiBroad Institute
Mitja I KurkiMassachusetts General Hospital
Andrea GannaBroad Institute
Andrea GannaMassachusetts General Hospital
Andrea GannaBroad Institute
Andrea GannaMassachusetts General Hospital
Benjamin GlaserHadassah-Hebrew University Medical Center
Gil AtzmonAlbert Einstein College of Medicine
Gil AtzmonUniversity of Haifa
Nir BarzilaiAlbert Einstein College of Medicine
Nikolas PontikosUniversity College London
Nikolas PontikosUCL Genetics Institute, University College London
Ben WeisburdBroad Institute
Ben WeisburdMassachusetts General Hospital
Ben WeisburdBroad Institute
Ben WeisburdMassachusetts General Hospital
Monkol LekBroad Institute
Monkol LekMassachusetts General Hospital
Konrad J KarczewskiBroad Institute
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiBroad Institute
Konrad J KarczewskiMassachusetts General Hospital
Eric Vallabh MinikelBroad Institute
Eric Vallabh MinikelMassachusetts General Hospital
Stefan SchreiberUniversity Hospital Schleswig-Holstein
Aarno PalotieBroad Institute
Aarno PalotieMassachusetts General Hospital
Aarno PalotieInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Steven R BrantJohns Hopkins University
Steven R BrantBloomberg School of Public Health, Johns Hopkins University
Richard H DuerrUniversity of Pittsburgh School of Medicine
Richard H DuerrUniversity of Pittsburgh Graduate School of Public Health
Mark S SilverbergMount Sinai Hospital
John D RiouxResearch Center, Montreal Heart Institute
John D RiouxUniversite de Montreal
Andre FrankeInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink