Hyung-Goo Kim

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 5

Top Topics

Intellectual Disability

Candida Albicans

Autism Spectrum Disorder

Top Venues

Journal of cellular and molecular medicine

American journal of medical genetics. Part A

Molecular autism

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

Publications

Madiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz, Afif Ben-Mahmoud, Vijay Gupta, Hyung-Goo Kim, Barbara Vona
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades. Journal of cellular and molecular medicine 28 (8) (2024)
Madiha Shadab, Ansar Ahmed Abbasi, Ahsan Ejaz, Afif Ben-Mahmoud, Vijay Gupta, Hyung-Goo Kim, Barbara Vona
Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades. Journal of cellular and molecular medicine 28 (8) (2024)
Sheng-Jia Lin, Barbara Vona, Hillary M Porter, Mahmoud Izadi, Kevin Huang, Yves Lacassie, Jill Anne Rosenfeld, Saadullah Khan, Cassidy Petree, Tayyiba Akbar Ali, Nazif Muhammad, Sher Alam Khan, Noor Muhammad, Pengfei Liu, Marie-Louise Haymon, Franz Rüschendorf, Il-Keun Kong, Linda Schnapp, Natasha Shur, Lynn P Chorich, Lawrence C Layman, Thomas Haaf, Ehsan Pourkarimi, Hyung-Goo Kim, Guarav K Varshney
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function. Human mutation 43 (10) (2022)
Matheus Augusto Araujo Castro, Juliana Heather Vedovato Dos Santos, Rachel Sayuri Honjo Kawahira, Guilherme Lopes Yamamoto, Debora Romeo Bertola, Anna C E Hurst, Lynn P Chorich, Lawrence C Layman, Chong Ae Kim, Hyung-Goo Kim
Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome. American journal of medical genetics. Part A 185 (12) (2021)
Hyung-Goo Kim, Jill A Rosenfeld, Daryl A Scott, Gerard Bénédicte, Jonathan D Labonne, Jason Brown, Marianne McGuire, Sonal Mahida, Sakkubai Naidu, Jacqueline Gutierrez, Gaetan Lesca, Vincent des Portes, Ange-Line Bruel, Arthur Sorlin, Fan Xia, Yline Capri, Eric Muller, Dianalee McKnight, Erin Torti, Franz Rüschendorf, Oliver Hummel, Zeyaul Islam, Prasanna R Kolatkar, Lawrence C Layman, Duchwan Ryu, Il-Keun Kong, Suneeta Madan-Khetarpal, Cheol-Hee Kim
Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism. Molecular autism 10 (2019)