Author

KE Wain

Observed name: K Wain

Institutions: Autism & Developmental Medicine Institute, Geisinger Health System

Observed institutions: Mayo Clinic, Autism & Developmental Medicine Institute, Geisinger Health System

OpenAlex ID: A5055882334

Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype

2012 · N Hoppman‐Chaney, K Wain, et al. · Clinical Genetics · 133

Towards an evidence‐based process for the clinical interpretation of copy number variation

2011 · ER Riggs, DM Church, et al. · Clinical Genetics · 122

Higher scores on autonomic symptom scales in pediatric patients with neurodevelopmental disorders of known genetic etiology

2022 · Antoinette S DiCriscio, KE Wain, et al. · Brain and Behavior · 4

Author response for "Higher scores on autonomic symptom scales in pediatric patients with neurodevelopmental disorders of known genetic etiology"

2022 · Antoinette S DiCriscio, KE Wain, et al. · Publons reviews and discussion

Author response for "Higher scores on autonomic symptom scales in pediatric patients with neurodevelopmental disorders of known genetic etiology"

2022 · Antoinette S DiCriscio, KE Wain, et al. · Publons reviews and discussion

Works count: 5

Citation count: 259

H-index: 3

I10-index: 2