Khushnooda Ramzan

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 5

Top Venues

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Annals of dermatology

Case reports in genetics

American journal of medical genetics. Part A

King Faisal Specialist Hospital & Research Centre

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

Affiliation History

King Faisal Specialist Hospital & Research Centre May 05 2007

Saudi Arabia

Scientist :: Department of Genetics

Publications

Aziza M Mushiba, Eissa Faqeih, Mohammed A Saleh, Khushnooda Ramzan, Faiqa Imtiaz, Mohammed Al-Owain, Amal M Alhashem, Abdulrahman Alswaid
The genotypic and phenotypic spectrum of pycnodysostosis in Saudi Arabia: Novel variants and clinical findings. American journal of medical genetics. Part A 185 (8) (2021)
Khushnooda Ramzan, Nouf S Al-Numair, Sarah Al-Ageel, Lina Elbaik, Nadia Sakati, Selwa A F Al-Hazzaa, Mohammed Al-Owain, Faiqa Imtiaz
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes 11 (12) (2020)
Khushnooda Ramzan, Mohammed Al-Owain, Nouf S Al-Numair, Sibtain Afzal, Sarah Al-Ageel, Sultan Al-Amer, Lina Al-Baik, Ghoson F Al-Otaibi, Amal Hashem, Eman Al-Mashharawi, Sulman Basit, Abdal H Al-Mazroea, Ameen Softah, Sameera Sogaty, Faiqa Imtiaz
Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 183 (3) (2019)
Alia M Albalawi, Jamil A Hashmi, Fatima Alfadhli, Ahmed M Almatrafi, Khushnooda Ramzan, Sulman Basit
Missense Mutations in the CTSC Gene in Saudi Families Segregating Papillon-Lefèvre Syndrome. Annals of dermatology 32 (1) (2019)
Salma M Wakil, Dorota Monies, Samya Hagos, Fahad Al-Ajlan, Josef Finsterer, Aisha Al Qahtani, Khushnooda Ramzan, Rawan Al Humaidy, Mohamed A Al-Muhaizea, Brian Meyer, Saeed A Bohlega
Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene. Case reports in genetics 2018 (2018)

Khushnooda Ramzan.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Khushnooda Ramzan