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Office
Division of Clinical Genetics
2401 Gillham Road
Kansas City, MO 64108Phone+1 816-302-3290Fax+1 816-302-9963
Summary
- Board certified in Clinical Biochemical Genetics; Clinical Genetics and Genomics; Pediatrics
Interests: rare diseases; mitochondrial disorders; neurogenetics; leukodystrophies; long-chain fatty acid oxidation disorders; methylmalonic acidemia and propionic acidemia; urea cycle disorders; PKU.
Education & Training
- Yale-New Haven HospitalFellowship, Clinical Biochemical Genetics, 2013 - 2014
- University of ConnecticutResidency, Medical Genetics and Genomics, 2011 - 2013
- University of ConnecticutResidency, Pediatrics, 1997 - 2000
- Uconn School Of MedicineClass of 1997
- Boston CollegeBS, Biology, Cum laude, 1989 - 1993
Certifications & Licensure
- KS State Medical License 2014 - 2025
- MO State Medical License 2014 - 2025
- CT State Medical License 2006 - 2022
- MA State Medical License 2001 - 2008
- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- House Officers' Award for Excellence in Teaching University of Connecticut School of Medicine Pediatric Residency Program, 2000
Clinical Trials
- Study of HST5040 in Subjects With Propionic or Methylmalonic Acidemia Start of enrollment: 2021 Mar 15
Publications & Presentations
PubMed
- Hypoglycemia in a 4-day-old Girl.Elizabeth C Loughman, Jennifer Gannon, Jotishna Sharma, Christopher R Nitkin
Pediatrics in Review. 2024-03-01 - 5 citationsInsurance denials and diagnostic rates in a pediatric genomic research cohort.Tricia N Zion, Courtney D Berrios, Ana S A Cohen, Lauren Bartik, Laura A Cross
Genetics in Medicine. 2023-05-01 - 36 citationsGenomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.Ana S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, Joseph T Alaimo, Shivarajan M Amudhavalli
Genetics in Medicine. 2022-06-01
Journal Articles
- Points to Consider When Assessing Relationships (Or Suspecting Misattributed Relationships) During Family-Based Clinical Genomic Testing: A Statement of the American C...Joshua L Deignan 1 , Elizabeth Chao 2 , Jennifer L Gannon 3 4 , Henry T Greely 5 , Kelly D Farwell Hagman 6 , Rong Mao 7 , Scott Topper 8 , ACMG Laboratory Qu..., Genetics in Medicine, 5/14/2020
- Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disabilityJennifer Malinowski PhD, David T. Miller MD, PhD, Laurie Demmer MD, Jennifer Gannon MD, Elaine Maria Pereira MD, Molly C. Schroeder PhD, Maren T. Scheuner MD, Anne Chu..., Genetics in Medicine, 3/23/2020
- Diagnostic Gene Sequencing Panels: From Design to Report-A Technical Standard of the American College of Medical Genetics and Genomics (ACMG)Lora J H Bean 1 2 , Birgit Funke 3 4 , Colleen M Carlston 5 , Jennifer L Gannon 6 7 , Sibel Kantarci 8 , Bryan L Krock 9 , Shulin Zhang 10 , Pinar Bayrak-..., Genetics in Medicine, 3/22/2020
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Abstracts/Posters
- Standardized care model to improve outcome for newborns with inborn error of metabolism requiring urgent dialysis therapy.Chadha V, Garg U, Thompson M, Daniel J, Rowzer K, Heese B, Gannon J., World Congress of Nephrology, Abu Dhabi, UAE., 3/26/2020
- Newborn screening for four lysosomal storage disorders: one center’s experience over six years.Strenk M, Gadea R, Heese BA, Gannon J., National Society of Genetic Counselors 38th Annual Conference, Salt Lake City, Utah., 11/5/2019
- Cutaneous manifestations of holocarboxylase synthetase deficiency.Duffy EK, Newell B, Gannon J, Nopper AJ., 13th World Congress of Pediatric Dermatology, Chicago, Illinois., 7/6/2017
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Professional Memberships
- Member
- Fellow
- American College of Medical Genetics and GenomicsFellow
- Society of Inherited Metabolic DisordersMember
- Mitochondrial Medicine SocietyMember
- Society for the Study of Inborn Errors of MetabolismMember
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