Mo Alisa - Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine

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论文共 24 篇作者统计合作学者相似作者

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Novel Phenotypes and Genotype-Phenotype Correlations in a Large Clinical Cohort of Patients with Kleefstra Syndrome

Zoe J. Frazier, Seyda Kilic, Hailey Osika,Alisa Mo, Meg Quinn, Sonia Ballal, Tamar Katz, A. Eliot Shearer, Max A. Horlbeck,Lynn S. Pais,Kira A. Dies,Anne O'Donnell-Luria, Joe Kossowsky, Jonathan O. Lipton,Tjitske Kleefstra,Siddharth Srivastava

CLINICAL GENETICS (2025)

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Approach to Diagnosis and Management of Genetic Neurodevelopmental Disorders

Alisa Mo, Michael Oanea,Julie S. Cohen,Lance Rodan,Siddharth Srivastava

Capute and Accardo' s Neurodevelopmental Disabilities in Infancy and Childhoodpp.487-507, (2025)

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Clinical and Neuropsychological Phenotyping of Individuals with Somatic Variants in Neurodevelopmental Disorders

Alisa Mo,Christopher A Walsh

Neurology Geneticsno. 2 (2025): e200254-e200254

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Cell-type-specific Effects of Autism-Associated 15q Duplication Syndrome in the Human Brain

Caroline Dias,Alisa Mo, Chunhui Cai,Liang Sun, Kristen Cabral,Catherine A. Brownstein,Shira Rockowitz,Christopher A. Walsh

AMERICAN JOURNAL OF HUMAN GENETICS（2024）

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Cell-type-specific Effects of Autism-Associated Chromosome 15Q11.2-13.1 Duplications in Human Brain

Caroline Dias,Alisa Mo, Chunhui Cai,Liang Sun, Kristen Cabral,Catherine A Brownstein,Shira Rockowitz,Christopher A Walsh

bioRxiv the preprint server for biology (2024)

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A Recurrent De Novo Variant in NUSAP1 Escapes Nonsense‐mediated Decay and Leads to Microcephaly, Epilepsy, and Developmental Delay

Alisa Mo,Emuna Paz-Ebstein,Shira Yanovsky-Dagan,Abbe Lai,Hagar Mor-Shaked,Tal Gilboa,Edward Yang,Diane D. Shao,Christopher A. Walsh,Tamar Harel

CLINICAL GENETICS（2023）

引用6浏览0WOS引用

TMEM161B Regulates Cerebral Cortical Gyration, Sonic Hedgehog Signaling, and Ciliary Structure in the Developing Central Nervous System

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAno. 4 (2023)

引用13浏览0WOS引用

The Clinical and Molecular Spectrum of ZFYVE26-associated Hereditary Spastic Paraplegia: SPG15

Afshin Saffari,Catherine Jordan,Alisa Mo,Bo Zhang,Mustafa Sahin,Craig Blackstone,Edward Yang,Darius Ebrahimi-Fakhari

NEUROLOGY（2023）

引用5浏览0WOS引用

The Clinical and Molecular Spectrum of ZFYVE26-Associated Hereditary Spastic Paraplegia (SPG15) (P13-11.005)

Afshin Saffari,Catherine Jordan,Alisa Mo,Bo Zhang,Mustafa Sahin,Craig Blackstone,Edward Yang,Darius Ebrahimi-Fakhari

Neurology（2023）

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Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria

JAMA NEUROLOGYno. 9 (2023): 980-988

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