Hind Alsharhan

ORCID

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 10

Top Venues

Genes

Journal of inherited metabolic disease

Neurology. Genetics

American journal of medical genetics. Part A

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

Publications

Nada T Alzayed, Abdullah H Alzuabi, Reem A Alqusaimi, Ehab A El-Anany, Abdullah Alholle, Ashraf H Aboelanine, Sherief Omar, Rasha Alsafi, Alaa A Elmonairy, Fatemah J Alali, Ahmad Alahmad, Hind Alsharhan, Buthaina Albash, Dana Marafi
Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1 -Related Disorder. Neurology. Genetics 10 (3) (2024)
Nada T Alzayed, Abdullah H Alzuabi, Reem A Alqusaimi, Ehab A El-Anany, Abdullah Alholle, Ashraf H Aboelanine, Sherief Omar, Rasha Alsafi, Alaa A Elmonairy, Fatemah J Alali, Ahmad Alahmad, Hind Alsharhan, Buthaina Albash, Dana Marafi
Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1 -Related Disorder. Neurology. Genetics 10 (3) (2024)
Noor Almoosawy, Fawaz Albaghli, Haya H Al-Balool, Hanan Fathi, Waleed A Zakaria, Mariam Ayed, Hind Alsharhan
Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies-Expanding the Phenotype. Genes 14 (6) (2023)
Noor Almoosawy, Fawaz Albaghli, Haya H Al-Balool, Hanan Fathi, Waleed A Zakaria, Mariam Ayed, Hind Alsharhan
Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies-Expanding the Phenotype. Genes 14 (6) (2023)
Maryam Aburezq, Ahmad Alahmad, Rasha Alsafi, Asma Al-Tawari, Dina Ramadan, Magdy Shafik, Omar Abdelaty, Nawal Makhseed, Reem Elshafie, Mariam Ayed, Abrar Hayat, Fatima Dashti, Dana Marafi, Buthaina Albash, Laila Bastaki, Hind Alsharhan
Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants. Orphanet journal of rare diseases 18 (1) (2023)
Noor Almoosawy, Fawaz Albaghli, Haya H Al-Balool, Hanan Fathi, Waleed A Zakaria, Mariam Ayed, Hind Alsharhan
Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies-Expanding the Phenotype. Genes 14 (6) (2023)
Noor Almoosawy, Fawaz Albaghli, Haya H Al-Balool, Hanan Fathi, Waleed A Zakaria, Mariam Ayed, Hind Alsharhan
Interstitial Deletion of 3q21 in a Kuwaiti Child with Multiple Congenital Anomalies-Expanding the Phenotype. Genes 14 (6) (2023)
Hind Alsharhan, Bobby G Ng, Earnest James Paul Daniel, Jennifer Friedman, Eniko K Pivnick, Amal Al-Hashem, Eissa Ali Faqeih, Pengfei Liu, Nicole M Engelhardt, Kierstin N Keller, Jie Chen, Pamela A Mazzeo, null null, Jill A Rosenfeld, Michael J Bamshad, Deborah A Nickerson, Kimiyo M Raymond, Hudson H Freeze, Miao He, Andrew C Edmondson, Christina Lam
Expanding the phenotype, genotype and biochemical knowledge of ALG3-CDG. Journal of inherited metabolic disease 44 (4) (2021)
Hind Alsharhan, Colleen Muraresku, Rebecca D Ganetzky
COXPD9 in an individual from Puerto Rico and literature review. American journal of medical genetics. Part A 185 (8) (2021)
Hind Alsharhan, Miao He, Andrew C Edmondson, Earnest J P Daniel, Jie Chen, Tyhiesia Donald, Somayeh Bakhtiari, David J Amor, Elizabeth A Jones, Grace Vassallo, Marie Vincent, Benjamin Cogné, Wallid Deb, Arend H Werners, Sheng C Jin, Kaya Bilguvar, John Christodoulou, Richard I Webster, Katherine R Yearwood, Bobby G Ng, Hudson H Freeze, Michael C Kruer, Dong Li, Kimiyo M Raymond, Elizabeth J Bhoj, Andrew K Sobering
ALG13 X-linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes. Journal of inherited metabolic disease 44 (4) (2021)

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Publication Activity (10 Years)

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Hind Alsharhan