Skip to Main Content

Paper Details

Rare penetrant mutations confer severe risk of common diseases.
medRxiv
0
2023
Rare variant, common diseases, common variants, human, phenotype-associated genes
Author NameAffiliation
Tobias HampInc. San Diego
François AguetInc. San Diego
Tomas Marques-BonetInstitute of Evolutionary Biology (UPF-CSIC) 08003 Barcelona
Tomas Marques-BonetInstitut Catala de Paleontologia Miquel Crusafont, Universitat Autonoma de Barcelona 08193 Barcelona
Tomas Marques-BonetBarcelona Institute of Science and Technology (BIST) 08003 Barcelona
Tomas Marques-BonetCatalan Institution of Research and Advanced Studies (ICREA) 08010 Barcelona
Tomas Marques-BonetInstitute of Evolutionary Biology (UPF-CSIC) 08003 Barcelona
Tomas Marques-BonetCatalan Institution of Research and Advanced Studies (ICREA) 08010 Barcelona
Tomas Marques-BonetBarcelona Institute of Science and Technology (BIST) 08003 Barcelona
Tomas Marques-BonetInstitut Catala de Paleontologia Miquel Crusafont, Universitat Autonoma de Barcelona 08193 Barcelona
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital
Heidi L RehmMassachusetts General Hospital Boston
Heidi L RehmBroad Institute of MIT and Harvard Cambridge
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital
Heidi L RehmBroad Institute of MIT and Harvard Cambridge
Heidi L RehmMassachusetts General Hospital Boston
Anne O'Donnell-LuriaBroad Institute of MIT and Harvard Cambridge
Anne O'Donnell-LuriaMassachusetts General Hospital Boston
Anne O'Donnell-LuriaBoston Children's Hospital Boston
Anne O'Donnell-LuriaBroad Institute of MIT and Harvard Cambridge
Anne O'Donnell-LuriaMassachusetts General Hospital Boston
Anne O'Donnell-LuriaBoston Children's Hospital Boston
Amit KheraCenter for Genomic Medicine, Massachusetts General Hospital
Amit KheraBroad Institute of MIT and Harvard Cambridge
Amit Khera
  • 1 - 25

Datasets

Release 1.2