Tara Wenger - Concepedia

Author

Tara Wenger

Also Known As

James T. Bennett, Jordan Whitlock, Lumaka, Lynne A. Wolfe, Mark Wener, Matthew T. Wheeler, Satid Thammasitboon, Stefano Gustincich, T L Wenger, T WENGER

127

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Seattle Children's Hospital Children's Hospital of Philadelphia University of Washington University of Pennsylvania Boston Children's Hospital

About

Tara Wenger is an author at Seattle Children's Hospital specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	918
2	Public Health	3	3	47
3	Education	2	2	25
4	Social Sciences	2	2	61
5	Anatomy	1	1	31

Tara Wenger

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Targeted long-read sequencing identifies missing disease-causing variation Danny E. Miller, Arvis Sulovari, Tianyun Wang, The American Journal of Human Genetics Long-read SequencingLong-read Sequencing IdentifiesNext-generation SequencingGenomicsMedicine	2021	227
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor Dong Li, Michael March, Álvaro Gutiérrez-Uzquiza, Nature Medicine Lymphoid NeoplasiaAutoimmune DiseaseImmunodeficienciesPathogenesisAutophagy	2019	213
Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly Dong Li, Tara Wenger, Christoph Seiler, Human Molecular Genetics Ephb4 MutationGeneticsMtorc1 ActivityImmunologyGenomic Mechanism	2018	98
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening Tara Wenger, Judith S. Miller, Lauren M. DePolo, Molecular Autism	2016	96
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants Samuel J. R. A. Chawner, Joanne Doherty, Richard Anney, American Journal of Psychiatry	2021	95
Phenotypes and genotypes in individuals with <i>SMC1A</i> variants Sylvia Huisman, Paul A. Mulder, E. Redeker, American Journal of Medical Genetics Part A	2017	94
Critical region within 22q11.2 linked to higher rate of autism spectrum disorder Caitlin C. Clements, Tara Wenger, Alisa R. Zoltowski, Molecular Autism	2017	58
Telemedicine for genetic and neurologic evaluation in the neonatal intensive care unit Tara Wenger, Jeffrey S. Gerdes, Katherine S. Taub, Journal of Perinatology Neonatal ResuscitationNeurologic EvaluationWireless TelemedicineNeonatologyPediatric Intensive Care	2014	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

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