M E Suzanne Lewis (Suzanne K Lewis, Suzanne Lewis)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 9

Top Topics

Autism Spectrum Disorder

Duchenne Muscular Dystrophy

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

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

Publications

Zong Yi Ha, Chieko Chijiwa, M E Suzanne Lewis
Clinical and Molecular Characterization of a Novel Homozygous Frameshift Variant in AEBP1-Related Classical-like Ehlers Danlos Syndrome Type 2 with Comparison to Previously Reported Rare Cases. Genes 15 (4) (2024)
Zong Yi Ha, Chieko Chijiwa, M E Suzanne Lewis
Clinical and Molecular Characterization of a Novel Homozygous Frameshift Variant in AEBP1-Related Classical-like Ehlers Danlos Syndrome Type 2 with Comparison to Previously Reported Rare Cases. Genes 15 (4) (2024)
Zong Yi Ha, Chieko Chijiwa, M E Suzanne Lewis
Clinical and Molecular Characterization of a Novel Homozygous Frameshift Variant in AEBP1-Related Classical-like Ehlers Danlos Syndrome Type 2 with Comparison to Previously Reported Rare Cases. Genes 15 (4) (2024)
Zong Yi Ha, Chieko Chijiwa, M E Suzanne Lewis
Clinical and Molecular Characterization of a Novel Homozygous Frameshift Variant in AEBP1-Related Classical-like Ehlers Danlos Syndrome Type 2 with Comparison to Previously Reported Rare Cases. Genes 15 (4) (2024)
Silas J Y Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W Scherer, M E Suzanne Lewis
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant. Genes 14 (12) (2023)
Silas J Y Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W Scherer, M E Suzanne Lewis
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant. Genes 14 (12) (2023)
Silas J Y Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W Scherer, M E Suzanne Lewis
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant. Genes 14 (12) (2023)
Matthew A Budd, Kristina Calli, Lindy Samson, Jennifer Bowes, Anthony Y Y Hsieh, John C Forbes, Ari Bitnun, Joel Singer, Fatima Kakkar, Ariane Alimenti, Evelyn J Maan, M E Suzanne Lewis, Carole Gentile, Hélène C F Côté, Jason C Brophy
Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder. Viruses 10 (2) (2018)
Michael D Fountain, Emmelien Aten, Megan T Cho, Jane Juusola, Magdalena A Walkiewicz, Joseph W Ray, Fan Xia, Yaping Yang, Brett H Graham, Carlos A Bacino, Lorraine Potocki, Arie van Haeringen, Claudia A L Ruivenkamp, Pedro Mancias, Hope Northrup, Mary K Kukolich, Marjan M Weiss, Conny M A van Ravenswaaij-Arts, Inge B Mathijssen, Sebastien Levesque, Naomi Meeks, Jill Anne Rosenfeld, Danielle Lemke, Ada Hamosh, M E Suzanne Lewis, Simone Race, Laura L Stewart, Beverly Hay, Andrea M Lewis, Rita L Guerreiro, Jose T Bras, Marcia P Martins, Gerarda Derksen-Lubsen, Els Peeters, Connie Stumpel, Sander Stegmann, Levinus A Bok, Gijs W E Santen, Christian Patrick Schaaf
The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families. Genetics in medicine : official journal of the American College of Medical Genetics 19 (1) (2016)