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Arthur S Lee

Years Active: 2019-2019
Publications (10 Years): 2

Broad Institute

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

Affiliation History

Broad Institute

United States

Postdoctoral Scholar :: MPG

Publications

Arthur S Lee, Jannette Rusch, Ana C Lima, Abul Usmani, Ni Huang, Maarja Lepamets, Katinka A Vigh-Conrad, Ronald E Worthington, Reedik Mägi, Xiaobo Wu, Kenneth I Aston, John P Atkinson, Douglas T Carrell, Rex A Hess, Brendan J Houston, Donald F Conrad
Rare mutations in the complement regulatory gene CSMD1 are associated with male and female infertility. Nature communications 10 (1) (2019)
Suzanna G M Frints, Friederike Hennig, Roberto Colombo, Sebastien Jacquemont, Paulien Terhal, Holly H Zimmerman, David Hunt, Bryce A Mendelsohn, Ulrike Kordaß, Richard Webster, Margje Sinnema, Omar Abdul-Rahman, Vanessa Suckow, Alberto Fernández-Jaén, Kees van Roozendaal, Servi J C Stevens, Merryn V E Macville, Salwan Al-Nasiry, Koen van Gassen, Norbert Utzig, Suzanne M Koudijs, Lesley McGregor, Saskia M Maas, Diana Baralle, Abhijit Dixit, Peter Wieacker, Marcus Lee, Arthur S Lee, Elizabeth C Engle, Gunnar Houge, Gyri A Gradek, Andrew G L Douglas, Cheryl Longman, Shelagh Joss, Danita Velasco, Raoul C M Hennekam, Hiromi Hirata, Vera M Kalscheuer
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita. Human mutation 40 (12) (2019)

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