Erica Davis - Dissemin

All papers authored by Erica Davis

This paper is made freely available by the publisher.

2023 Victoria Patterson

, Farid Ullah

, Laura Bryant

, Dong Li, John N. Griffin, Alpa Sidhu

, Sheila Saliganan, Mackenzie Blaile, Margarita S. Saenz

, Rosemarie Smith, Sara Ellingwood, Dorothy K. Grange

, Xuyun Hu

, Maimaiti Mireguli, Yanfei Luo and 37 other authors

Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish

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2022 Laura J. Grange

, John J. Reynolds

, Farid Ullah, Bertrand Isidor, Robert F. Shearer

, Xenia Latypova, Ryan M. Baxley

, Antony W. Oliver

, Anil Ganesh, Sophie L. Cooke

, Satpal S. Jhujh

, Gavin S. McNee, Robert Hollingworth, Martin R. Higgs

, Toyoaki Natsume and 33 other authors

Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidy

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2021 Farid Ullah, Waqar Rauf, Kamal Khan, Sheraz Khan, Katrina M. Bell, Vanessa Cristina de Oliveira

, Muhammad Tariq, Shabnam Bakhshalizadeh, Philippe Touraine, Nicholas Katsanis, Andrew Sinclair, Sijie He, Elena J. Tucker, Shahid M. Baig, Erica E. Davis

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss

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2019 Kamal Khan

, Michael Zech

, Angela T. Morgan, Matej Skorvanek

, Tahir N. Khan, Michael S. Hildebrand, Victoria E. Jackson

, Thomas S. Scerri

, Kristin A. Rigbye, Ingrid E. Scheffer

, Matias Wagner

, Daniel D. Lam

, Petra Havránková, Anna Fečíková

, Tim M. Strom and 15 other authors

Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia

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2017 Benjamin M. Helm, Jason R. Willer

, Azita Sadeghpour, Christelle Golzio, Eric Crouch, Samantha Schrier Vergano, Nicholas Katsanis

, Erica E. Davis

Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome

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2014 Susan S. Brooks

, Alissa L. Wall, Christelle Golzio, David W. Reid, Amalia Kondyles, Jason R. Willer

, Christina Botti, Christopher V. Nicchitta, Nicholas Katsanis, Erica E. Davis

A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrupts Neurodevelopment and Causes X-Linked Microcephaly in Humans

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All papers authored by Erica Davis