Lee-kai Wang - Concepedia

Author

Lee-kai Wang

Also Known As

Jennifer Wambach, Jijun Wan, Lee-Kai Wang, Lee-kai Wang, Lynne A. Wolfe, Margot R.F. Reijnders, Mark Wener, Matthew T. Wheeler, Milena Mariani, Monte Westerfield

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Boston Children's Hospital Columbia University University of California, Los Angeles Baylor College of Medicine Washington University in St. Louis

About

Lee-kai Wang is an author at Boston Children's Hospital specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	444
2	Social Sciences	4	4	143
3	Neurology	2	2	102
4	Behavioral Sciences	1	1	468
5	Genomic Medicine	1	1	39

Lee-kai Wang

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks Elizabeth K. Ruzzo, Laura Pérez‐Cano, Jae-Yoon Jung, Cell Behavioral SciencesSyndromic AutismGeneticsAutismNeurodiversity	2019	468
Diagnostic utility of transcriptome sequencing for rare Mendelian diseases Hane Lee, Alden Huang, Lee-kai Wang, Genetics in Medicine SequencingMendelian DisorderDiagnostic UtilityMedicineGenetics	2019	207
Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia Minsoo Kim, Jillian R. Haney, Pan Zhang, Nature Neuroscience Complement SystemConvergent Synaptic PathologySignal TransductionMolecular NeurosciencePsychiatry	2021	72
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia Oguz Kanca, Jonathan C. Andrews, Pei-Tseng Lee, The American Journal of Human Genetics Wdr37 Are AssociatedMendelian DisorderGenetic DisorderGeneticsDe Novo Variants	2019	55
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids Sacha Ferdinandusse, Kirsty McWalter, Heleen te Brinke, Genetics in Medicine	2020	49
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations Lance H. Rodan, Rebecca C. Spillmann, Harley T. Kurata, Genetics in Medicine Neurobiology Of DiseaseCorticobasal DegenerationNeurological DisorderIsolated Neurological ManifestationsPathology	2021	47
Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science Kelly Schoch, Cecilia Esteves, Anna Bican, Genetics in Medicine Undiagnosed Diseases NetworkTranslational BioinformaticsMedicineGeneticsGenetic Epidemiology	2020	39
Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases Shilpa N. Kobren, Dustin Baldridge, Matt Velinder, Genetics in Medicine	2021	32
Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain Felix Marbach, Georgi Stoyanov, Florian Erger, Genetics in Medicine	2021	27
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11 Thomas A. Ravenscroft, Jennifer B. Phillips, Elizabeth L. Fieg, Genetics in Medicine	2021	26

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