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Paper Details

TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci.
Hum Mol Genet
8
2020
GnRH, GnRH dysfunction, GnRH neurons, IGD, Kallmann syndrome, STUB1 mRNA, TCF12, TCF12 haploinsufficiency, causal loci, gonadotropin-releasing hormone, isolated GnRH deficiency, stub1, syndromic, syndromic and non-syndromic craniosynostosis, tcf12, tcf3a/b, zebrafish
Author NameAffiliation
Irene ValenzuelaVall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus
Irene ValenzuelaVall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus
Margaret E WiermanUniversity of Colorado Anschutz Medical Campus
Taibo LiMassachusetts General Hospital
Taibo LiJohns Hopkins School of Medicine
Taibo LiBroad Institute of MIT and Harvard
Kasper LageHarvard Medical School
Kasper LageBroad Institute of MIT and Harvard
Kasper LageMassachusetts General Hospital
Nicholas KatsanisCenter for Human Disease Modeling, Duke University
Nicholas KatsanisAdvanced Center for Translational and Genetic Medicine (ACT-GeM), Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago
Nicholas KatsanisFeinberg School of Medicine, Northwestern University
Nicholas KatsanisCenter for Human Disease Modeling, Duke University
Nicholas KatsanisAdvanced Center for Translational and Genetic Medicine (ACT-GeM), Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago
Nicholas KatsanisFeinberg School of Medicine, Northwestern University
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