Michael J Lyons (M J Lyons)

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 4

Top Topics

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

AJNR. American journal of neuroradiology

Nature communications

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

Publications

Kameryn M Butler, Timothy Fee, Barbara R DuPont, Jane H Dean, Roger E Stevenson, Michael J Lyons
A SOX3 duplication and lumbosacral spina bifida in three generations. American journal of medical genetics. Part A 188 (5) (2022)
César Augusto Pinheiro Ferreira Alves, O Sherbini, F D'Arco, Dora Batia Dyne Steel, Manju A Kurian, F C Radio, Giovanbattista Giovanni Battista Ferrero, Diana Carli, Tartaglia Marco, Tuğçe B Balcı, N N Powell-Hamilton, S A Schrier Vergano, H Reutter, Julia Hoefele, R Günthner, Elizabeth R Roeder, R O Littlejohn, Davor Lessel, Sabine Peters, C Kentros, Kwame Anyane-Yeboa, Claudia B Catarino, Saadet Mercimek-Mahmutoglu, J Denecke, Michael J Lyons, Florentine Radelfahr, Elizabeth Joyce Bhoj, Laura Bryant, Adeline Vanderver
Brain Abnormalities in Patients with Germline Variants in H3F3 : Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors. AJNR. American journal of neuroradiology 43 (7) (2022)
Ilaria Parenti, Daphne Lehalle, Caroline Nava, Erin Torti, Elsa Leitão, Richard Person, Takeshi Mizuguchi, Naomichi Matsumoto, Mitsuhiro Kato, Kazuyuki Nakamura, Stella A de Man, Heidi Cope, Vandana Shashi, null null, Jennifer Friedman, Pascal Joset, Katharina Steindl, Anita Rauch, Irena Muffels, Peter M van Hasselt, Florence Petit, Thomas Smol, Gwenaël Le Guyader, Frederic Bilan, Arthur Sorlin, Antonio Vitobello, Christophe Philippe, Ingrid M B H van de Laar, Marjon A van Slegtenhorst, Philippe M Campeau, Ping Yee Billie Au, Mitsuko Nakashima, Hirotomo Saitsu, Tatsuya Yamamoto, Yumiko Nomura, Raymond J Louie, Michael J Lyons, Amy Dobson, Astrid S Plomp, M Mahdi Motazacker, Frank J Kaiser, Andrew T Timberlake, Sabine A Fuchs, Christel Depienne, Mignot Cyril
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy. Human genetics 140 (7) (2021)
Yu-Ri Lee, Kamal Khan, Kim Armfield-Uhas, Sujata Srikanth, Nicola A Thompson, Mercedes Calvo Pardo, Lu Yu, Joy W Norris, Yunhui Peng, Karen W Gripp, Kirk A Aleck, Chumei Li, Ed Spence, Tae-Ik Choi, Soo Jeong Kwon, Hee-Moon Park, Daseuli Yu, Seokhwi Kim, Marie R Mooney, Shahid M Baig, Ingrid M Wentzensen, Aida Telegrafi, Kirsty McWalter, Trevor A Moreland, Chelsea Roadhouse, Keri Ramsey, Michael J Lyons, Cindy Skinner, Emil Alexov, Nicholas Katsanis, Roger E Stevenson, Jyoti Sharma Choudhary, David J Adams, Cheol-Hee Kim, Erica E Davis, Charles E Schwartz
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nature communications 11 (1) (2020)