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JL

Jane B. Lane

University of Alabama at Birmingham US

ORCID iD 0000-0003-0602-9325
75
Publications
4,301
Citations
38
H-Index
50
i10-Index
4.33
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex . OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

75 total

Longitudinal course of epilepsy in Rett syndrome and related disorders PDF

Daniel Tarquinio, Wei Hou, Anne T. Berg, Walter E. Kaufmann, Jane B. Lane et al. - Brain, 2016
Cited by 127 OpenAlex

<i>Methyl-CpG-binding protein 2</i> (<i>MECP2</i>) mutation type is associated with disease severity in Rett syndrome PDF

Vishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, Jane B. Lane, Kathleen J. Motil et al. - Journal of Medical Genetics, 2014
Cited by 313 OpenAlex

Developmental delay in Rett syndrome: data from the natural history study PDF

Jeffrey L. Neul, Jane B. Lane, Hye Seung Lee, Suzanne Geerts, Judy O. Barrish et al. - Journal of Neurodevelopmental Disorders, 2014
Cited by 163 OpenAlex

Gastrointestinal and Nutritional Problems Occur Frequently Throughout Life in Girls and Women With Rett Syndrome

Kathleen J. Motil, Erwin Caeg, Judy O. Barrish, Suzanne Geerts, Jane B. Lane et al. - Journal of Pediatric Gastroenterology and Nutrition, 2012
Cited by 207 OpenAlex

Growth failure and outcome in Rett syndrome PDF

Daniel Tarquinio, Kathleen J. Motil, Wei Hou, Hye Seung Lee, Daniel G. Glaze et al. - Neurology, 2012
Cited by 122 OpenAlex

Epilepsy and the natural history of Rett syndrome PDF

Daniel G. Glaze, Alan K. Percy, Steven A. Skinner, Kathleen J. Motil, Jeffrey L. Neul et al. - Neurology, 2010
Cited by 221 OpenAlex

Rett syndrome diagnostic criteria: Lessons from the Natural History Study PDF

Alan K. Percy, Jeffrey L. Neul, Daniel G. Glaze, Kathleen J. Motil, Steven A. Skinner et al. - Annals of Neurology, 2010
Cited by 146 OpenAlex

Specific mutations in <i>Methyl-CpG-Binding Protein 2</i> confer different severity in Rett syndrome PDF

Jeffrey L. Neul, Ping Fang, James P. Barrish, Jane B. Lane, Erwin Caeg et al. - Neurology, 2008
Cited by 499 OpenAlex

Phenotypic manifestations of <i>MECP2</i> mutations in classical and atypical rett syndrome

Carolyn Schanen, Elisa J. F. Houwink, Naghmeh Dorrani, Jane B. Lane, Ruth Everett et al. - American Journal of Medical Genetics Part A, 2003
Cited by 123 OpenAlex

Research Topics

Genetics and Neurodevelopmental Disorders (57) Autism Spectrum Disorder Research (26) Family and Disability Support Research (18) Neurogenetic and Muscular Disorders Research (13) Child Nutrition and Feeding Issues (9)

Affiliations

Boston Children's Hospital
US 2019 - 2019
University of Alabama at Birmingham Hospital
US 2024 - 2024
Children's National
US 2003 - 2003
University of South Carolina
US 2019 - 2019
University of Alabama
US 2013 - 2013

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