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Research Interests

Papers共 393 篇Author StatisticsCo-AuthorSimilar Experts

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期刊级别
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P252: Reanalysis of Pediatric Exome and Genome Sequencing Identifies a High Prevalence of Actionable Pharmacogenetic Alleles in Children
Rasika Venkatesh, Anthony Gacita, Manuel Torres Diz,Karl Keat, Ian Campbell,Ingo Helbig, Marylyn Ritchie
Genetics in Medicine Open (2025): 102217
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Clinical Signatures of SYNGAP1-related Disorders Through Data Integration
Jillian L McKee, Jan H Magielski,Julie Xian, Stacey Cohen, Jonathan Toib, Alicia Harrison, Chen, Dan Kim, Aakash Rathod, Elise Brimble, Nasha Fitter, J Michael Graglia, Kathryn A Helde, Sarah McKeown Ruggiero, Michael J Boland,Benjamin L Prosser, Rob Sederman,Ingo Helbig
Genetics in medicine official journal of the American College of Medical Geneticsno. 6 (2025): 101419-101419
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Phenotypic Analysis of 11,125 Trio Exomes in Neurodevelopmental Disorders
Shiva Ganesan, Sarah M Ruggiero, Shridhar Parthasarathy, Peter D Galer, David Lewis-Smith, Ian McSalley, Stacey R Cohen,Laina Lusk, Anna J Prentice,Jillian L McKee,Manuela Pendziwiat,Lacey Smith, Yvonne Weber,Heather C Mefford,Annapurna Poduri,Ingo Helbig
bioRxiv the preprint server for biology (2025)
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Familial SYNGAP1 Variants Define the Boundaries of a Complex Neurodevelopmental Disorder with Epilepsy
Alicia G Harrison, Jan H Magielski, Ian McSalley, Shiva Ganesan, Anna J Prentice, Kristin G Cunningham,Samuel R Pierce, Michael J Boland, Benjamin L Prosser,Ingo Helbig,Jillian L McKee
Epilepsia (2025)
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Author Statistics

#Papers: 393

#Citation: 16815

H-Index: 68

G-Index: 122

Sociability: 9

Diversity: 3

Activity: 114

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