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Identification of De Novo Variants in Nonsyndromic Cleft Lip With/without Cleft Palate Patients with Low Polygenic Risk Scores

Nina Ishorst,Leonie Henschel,Frederic Thieme,Dmitriy Drichel,Sugirthan Sivalingam,Sarah L. Mehrem, Ariane C. Fechtner,Julia Fazaal,Julia Welzenbach,Andre Heimbach,Carlo Maj,Oleg Borisov,Jonas Hausen,Ruth Raff,Alexander Hoischen,Michael Dixon,Alvaro Rada-Iglesias,Michaela Bartusel,Augusto Rojas-Martinez,Khalid Aldhorae,Bert Braumann,Teresa Kruse,Christian Kirschneck,Gerrit Spanier,Heiko Reutter,Stefanie Nowak,Lina Goelz,Michael Knapp,Andreas Buness,Peter Krawitz,Markus M. Noethen,Michael Nothnagel,Tim Becker,Kerstin U. Ludwig,Elisabeth Mangold

Molecular Genetics & Genomic Medicine（2022）

Cited 4|Views17
Key words
candidate genes,de novo variants,exome sequencing,nonsyndromic cleft lip with,without cleft palate,polygenic risk,single-molecule molecular inversion probes
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