Yufei Shi

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 7

Top Venues

The Journal of clinical endocrinology and metabolism

BMC medical genetics

PloS one

Clinical endocrinology

King Faisal Specialist Hospital and Research Centre

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

Affiliation History

King Faisal Specialist Hospital and Research Centre

Saudi Arabia

Principal investigator :: Genetics

Publications

Meshael Alswailem, Balgees Alghamdi, Anwar Alotaibi, Abeer Aljomiah, Hindi Al-Hindi, Avaniyapuram Kannan Murugan, Mohamed Abouelhoda, Yufei Shi, Ali S Alzahrani
Molecular genetics of diffuse sclerosing papillary thyroid cancer. The Journal of clinical endocrinology and metabolism (2023)
Zayed Al-Zayed, Roua A Al-Rijjal, Lamya Al-Ghofaili, Huda A BinEssa, Rajeev Pant, Anwar Alrabiah, Thamer Al-Hussainan, Minjing Zou, Brian F Meyer, Yufei Shi
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostoses. Orphanet journal of rare diseases 16 (1) (2021)
Minjing Zou, Huda A BinEssa, Yousif H Al-Malki, Suhad Al-Yahya, Monther Al-Alwan, Ibrahim Al-Jammaz, Khalid S A Khabar, Falah Almohanna, Abdullah M Assiri, Brian F Meyer, Ali S Alzahrani, Futwan A Al-Mohanna, Yufei Shi
β-Catenin Attenuation Inhibits Tumor Growth and Promotes Differentiation in a BRAFV600E-Driven Thyroid Cancer Animal Model. Molecular cancer therapeutics 20 (9) (2021)
Najla Albader, Minjing Zou, Huda A BinEssa, Saba Abdi, Anwar F Al-Enezi, Brian F Meyer, Ali S Alzahrani, Yufei Shi
Insights of Non-canonical Splice-site Variants on RNA Splicing in Patients with Congenital Hypothyroidism. The Journal of clinical endocrinology and metabolism (2021)
Yılmaz Kor, Minjing Zou, Roua A Al-Rijjal, Dorota Monies, Brian F Meyer, Yufei Shi
Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling. BMC medical genetics 19 (1) (2018)
Sezer Acar, Huda A BinEssa, Korcan Demir, Roua A Al-Rijjal, Minjing Zou, Gönül Çatli, Ahmet Anık, Anwar F Al-Enezi, Seçil Özışık, Manar S A Al-Faham, Ayhan Abacı, Bumin Dündar, Walaa E Kattan, Maysoon Alsagob, Salih Kavukçu, Hamdi E Tamimi, Brian F Meyer, Ece Böber, Yufei Shi
Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3. PloS one 13 (3) (2018)
Ayla Guven, Roua A Al-Rijjal, Huda A BinEssa, Durmuş Dogan, Yılmaz Kor, Minjing Zou, Namik Kaya, Anwar F Alenezi, Suna Hancili, Ömer Tarım, Essa Y Baitei, Walaa E Kattan, Brian F Meyer, Yufei Shi
Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets. Clinical endocrinology 87 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Yufei Shi