Katrina M. Dipple - Concepedia

Author

Katrina M. Dipple

Also Known As

Ascia Eskin, Brent L. Fogel, Chia-Lin Wei, Dan Doherty, David D. Draper, Esteban C Dell’Angelica, Esteban C. Dell'Angelica, Esteban C. Dell’Angelica, K DIPPLE, K Dipple

167

Publications

6.2K

Citations

H-Index

106

Concepts

All Affiliations

University of California, Los Angeles Baylor College of Medicine University of Washington Columbia University Seattle Children's Hospital

About

Katrina M. Dipple is an author at University of California, Los Angeles specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	42	2.5K
2	Health Sciences	7	7	262
3	Natural Sciences	7	7	196
4	Engineering	3	3	279
5	Public Health	1	1	51

Katrina M. Dipple

Publications

4.2K

Citations

H-Index

Page 1

	Year	Citations
Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders Hane Lee, Joshua L. Deignan, Naghmeh Dorrani, JAMA	2014	969
Validation of candidate causal genes for obesity that affect shared metabolic pathways and networks Xia Yang, Joshua L. Deignan, Hongxiu Qi, Nature Genetics ObesityMetabolic SyndromeMetabolic NetworkMetabolic PathwaysGenetics	2009	281
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
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome Julia Wang, Rami Al‐Ouran, Yanhui Hu, The American Journal of Human Genetics	2017	217
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease Rachel Ramoni, John J. Mulvihill, David R. Adams, The American Journal of Human Genetics Disease DiagnosisNetwork ScienceHealth InformaticsData ScienceData Mining	2017	181
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway Justyna A. Karolak, Marie Vincent, Gail Deutsch, The American Journal of Human Genetics Developmental BiologyPulmonary PathologyMedicinePathologyBronchial Neoplasm	2019	162
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3 Hsiao‐Tuan Chao, Mariska Davids, Elizabeth A. Burke, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental AnomalyDevelopmental BiologySyndromic Neurodevelopmental DisorderMendelian Disorder	2016	118
IRF2BPL Is Associated with Neurological Phenotypes Paul C. Marcogliese, Vandana Shashi, Rebecca C. Spillmann, The American Journal of Human Genetics NeurologyNeuroscienceMolecular NeurobiologyNeuropathologyMedicine	2018	108
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay Keren Machol, Justine Rousseau, Sophie Ehresmann, The American Journal of Human Genetics	2018	88
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype Vandana Shashi, Loren D.M. Peña, Katherine Kim, The American Journal of Human Genetics Allelic VariantSystems BiologySomatic VariantGenetic DisorderGenetics	2016	86

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