Alpa Sidhu

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Tyrosine Kinase

Top Venues

Science advances

Molecular genetics & genomic medicine

Case reports in genetics

Clinical case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Victoria Patterson, Farid Ullah, Laura Bryant, John N Griffin, Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile, Margarita Sifuentes Saenz, Rosemarie Smith, Sara Ellingwood, Dorothy K Grange, Xuyun Hu, Maimaiti Mireguli, Yanfei Luo, Yiping Shen, Maureen S Mulhern, Elaine Zackai, Alyssa L Ritter, Kosaki Izumi, Julia Hoefele, Matias Wagner, Korbinian Maria Riedhammer, Barbara Seitz, Nathaniel H Robin, Dana Goodloe, Cyril Mignot, Boris Keren, Helen Cox, Joanna Jarvis, Maja Hempel, Cynthia Forster Gibson, Frédéric Tran Mau Them, Antonio Vitobello, Ange-Line Bruel, Arthur Sorlin, Sarju G Mehta, F Lucy Raymond, Kelly Gilmore, Bradford C Powell, Karen E Weck, Chumei Li, Anneke T Vulto-van Silfhout, Thea Giacomini, Maria Margherita Mancardi, Andrea Accogli, Vincenzo Salpietro, Federico Zara, Neeta L Vora, Erica E Davis, Rebecca D Burdine, Elizabeth Joyce Bhoj
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science advances 9 (17) (2023)
Victoria Patterson, Farid Ullah, Laura Bryant, John N Griffin, Alpa Sidhu, Sheila Saliganan, Mackenzie Blaile, Margarita Sifuentes Saenz, Rosemarie Smith, Sara Ellingwood, Dorothy K Grange, Xuyun Hu, Maimaiti Mireguli, Yanfei Luo, Yiping Shen, Maureen S Mulhern, Elaine Zackai, Alyssa L Ritter, Kosaki Izumi, Julia Hoefele, Matias Wagner, Korbinian Maria Riedhammer, Barbara Seitz, Nathaniel H Robin, Dana Goodloe, Cyril Mignot, Boris Keren, Helen Cox, Joanna Jarvis, Maja Hempel, Cynthia Forster Gibson, Frédéric Tran Mau Them, Antonio Vitobello, Ange-Line Bruel, Arthur Sorlin, Sarju G Mehta, F Lucy Raymond, Kelly Gilmore, Bradford C Powell, Karen E Weck, Chumei Li, Anneke T Vulto-van Silfhout, Thea Giacomini, Maria Margherita Mancardi, Andrea Accogli, Vincenzo Salpietro, Federico Zara, Neeta L Vora, Erica E Davis, Rebecca D Burdine, Elizabeth Joyce Bhoj
Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish. Science advances 9 (17) (2023)
Khaliunaa Bayanbold, Georgianne Younger, Benjamin W Darbro, Alpa Sidhu
Mosaicism in BRPF1 -Related Neurodevelopmental Disorder: Report of Two Sisters and Literature Review. Case reports in genetics 2023 (2023)
Logan Goetzinger, Rachel D Starks, Kyle Dillahunt, Heather Major, Jaime M Nagy, Alpa Sidhu
Interstitial duplication of 20q11.22q13.11: A case report and review of literature. Molecular genetics & genomic medicine 9 (8) (2021)
Emma Elizabeth Palmer, Chloe Whitton, Mais O Hashem, Robin D Clark, Subhadra Ramanathan, Lois J Starr, Danita Velasco, John Karl De Dios, Emily Singh, Valerie Cormier-Daire, Maya Chopra, Lance H Rodan, Christoffer Nellaker, Shenela Lakhani, Eric James Mallack, Karin Panzer, Alpa Sidhu, Ingrid M Wentzensen, Didier Lacombe, Vincent Michaud, Fowzan Sami Alkuraya
CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum. Clinical genetics 100 (4) (2021)
Steven Leary, Harry S Porterfield, Jaclyn R Kotlarek, Benjamin W Darbro, Alpa Sidhu
Interstitial duplication of 8q22.1-q23.1- A case report and review of the literature. Clinical case reports 7 (12) (2019)