Jeffrey W Innis
Professor Emeritus of Human Genetics
Professor Emeritus of Pediatrics
Professor Emeritus of Internal Medicine
[email protected]

Available to mentor
Jeffrey W Innis
Professor Emeritus/a
  • Recent Publications
    • Recent Publications See All Publications
    • Journal Article
      Personal journeys to and in human genetics and dysmorphology.
      Schwartz CE, Aylsworth AS, Allanson J, Battaglia A, Carey JC, Curry CJ, Davies KE, Eichler EE, Graham JM, Hall B, Hall JG, Holmes LB, Hoyme HE, Hunter A, Innis J, Johnson J, Keppler-Noreuil KM, Leroy JG, Moore C, Nelson DL, Neri G, Opitz JM, Picketts D, Raymond FL, Shalev SA, Stevenson RE, Stumpel CTRM, Sutherland G, Viskochil DH, Weaver DD, Zackai EH. Am J Med Genet A, 2024 Jun; 194 (6): e63514 DOI:10.1002/ajmg.a.63514
      PMID: 38329159
    • Journal Article
      A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification.
      Serpen JY, Presley W, Beil A, Armenti ST, Johnson K, Mian SI, Innis JW, Prasov L. Genes (Basel), 2023 May 1; 14 (5): DOI:10.3390/genes14051034
      PMID: 37239394
    • Journal Article
      Design and Outcomes of a Novel Multidisciplinary Ophthalmic Genetics Clinic.
      Parekh B, Beil A, Blevins B, Jacobson A, Williams P, Innis JW, Barone Pritchard A, Prasov L. Genes (Basel), 2023 Mar 15; 14 (3): DOI:10.3390/genes14030726
      PMID: 36980998
    • Proceeding / Abstract / Poster
      eP217: Ophthalmology genetics clinic in the times of COVID-19: A hybrid model
      Pritchard A, Beil A, Innis J, Prasov L. Genetics in Medicine, 2022 Mar; 24 (3): s135 DOI:10.1016/j.gim.2022.01.253
    • Proceeding / Abstract / Poster
      eP249: Practical implementation of inpatient rapid comprehensive sequencing for critically ill pediatric patients
      Sloan-Heggen C, Pritchard AB, Barks J, Dang L, Desch K, Quasney M, Russell M, Innis J. Genetics in Medicine, 2022 Mar; 24 (3): s158 DOI:10.1016/j.gim.2022.01.284
    • Proceeding / Abstract / Poster
      eP290: A mosaic Angelman syndrome case with language apraxia and symptoms overlapping Prader-Willi syndrome
      Yang C, Sloan-Heggen C, Ducharme N, Bienemann L, Sarchenko J, Kubisak A, LeSueur K, Hannibal M, Innis J. Genetics in Medicine, 2022 Mar; 24 (3): s183 - s184. DOI:10.1016/j.gim.2022.01.325
    • Journal Article
      Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability.
      Tayeh MK, DeVaul J, LeSueur K, Yang C, Bedoyan JK, Thomas P, Hannibal MC, Innis JW. Am J Med Genet A, 2022 Jul; 188 (7): 2209 - 2216. DOI:10.1002/ajmg.a.62752
      PMID: 35365979
    • Journal Article
      Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes.
      Mullegama SV, Klein SD, Williams SR, Innis JW, Probst FJ, Haldeman-Englert C, Martinez-Agosto JA, Yang Y, Tian Y, Elsea SH, Ezashi T. Sci Rep, 2021 May 28; 11 (1): 11295 DOI:10.1038/s41598-021-90798-z
      PMID: 34050248