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Erica E. Davis
Affiliation : Northwestern University · Lurie Children's Hospital
- 4Publications (affiliation in the United States)
- 185Total publications
- 11114Citations
- 60h-index
Research profile
Erica E. Davis has 4 indexed publications (2010–2024). Their work appears mainly in “medRxiv”, “The American Journal of Human Genetics” and “Nature Genetics”. Their most cited article, “Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes” (2010), has been cited 282 times. Their work is co-authored with at least 12 researchers, including institutions in United Kingdom, Kuwait, Japan, Russia.
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Create my free profile Add my publicationsResearch areas
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Cystic Fibrosis Research Advances
- Genetics and Neurodevelopmental Disorders
- Hereditary Neurological Disorders
Publications (4)
- RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS
- Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type
- Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
- Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease
Publication venues
- medRxiv × 1
- The American Journal of Human Genetics × 1
- Nature Genetics × 1
- Human Genetics × 1
Publications per year
- 20241
- 20151
- 20102
Collaborations
Partner institutions : Baylor College of Medicine · Howard Hughes Medical Institute · Columbia University Irving Medical Center · University of California San Diego · Johns Hopkins University
Co-authors’ countries : United Kingdom · Kuwait · Japan · Russia
Co-authors
- Nicholas Katsanis
- Guoling Tian
- Susanne Held
- Carsten Russ
- A. Arockia Jeyaprakash
- Jennifer L. Silhavy
- Kiara E. Moore
- Jeong Ho Lee
- Pengfei Liu
- Ji Eun Lee
- Zachari A. Kupchinsky
- Raey Yeneabat
Bibliographic data from OpenAlex (open database).
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