Sajid Malik

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 19

Top Venues

Journal of biosocial science

American journal of medical genetics. Part A

Asian biomedicine : research, reviews and news

European journal of human genetics : EJHG

Quaid-i-Azam University, Faculty of Biological Sciences

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

Affiliation History

Quaid-i-Azam University, Faculty of Biological Sciences

Pakistan

Professor :: Department of Zoology

Publications

Sajid Malik, Anisa Bibi, Rubbiya Farid, Sidra Khan, Javaid Awan, Atta Ur Rehman
Consanguinity in northwest Pakistan: evidence of temporal decline. Journal of biosocial science 56 (3) (2024)
Sajid Malik, Anisa Bibi, Rubbiya Farid, Sidra Khan, Javaid Awan, Atta Ur Rehman
Consanguinity in northwest Pakistan: evidence of temporal decline. Journal of biosocial science 56 (3) (2024)
Anisa Bibi, Weizhen Ji, Lauren Jeffries, Cynthia Zerillo, Monica Konstantino, Emily K Mis, Filza Khursheed, Mustafa K Khokha, Saquib A Lakhani, Sajid Malik
Exome sequencing reveals genetic heterogeneity in consanguineous Pakistani families with neurodevelopmental and neuromuscular disorders. American journal of medical genetics. Part C, Seminars in medical genetics (2024)
Sajid Malik, Anisa Bibi, Rubbiya Farid, Sidra Khan, Javaid Awan, Atta Ur Rehman
Consanguinity in northwest Pakistan: evidence of temporal decline. Journal of biosocial science 56 (3) (2024)
Sajid Malik, Anisa Bibi, Rubbiya Farid, Sidra Khan, Javaid Awan, Atta Ur Rehman
Consanguinity in northwest Pakistan: evidence of temporal decline. Journal of biosocial science (2024)
Muhammad Naeem, Bashir Ahmad, Sajid Malik
Burden of congenital and hereditary anomalies in the war-affected territory at Pakistan-Afghanistan border. Asian biomedicine : research, reviews and news 16 (6) (2023)
Anisa Bibi, Sader Uddin, Muhammad Naeem, Amman Syed, Waheed Ud-Din Qazi, Farooq Azam Rathore, Sajid Malik
Prevalence pattern, phenotypic manifestation, and descriptive genetics of congenital limb deficiencies in Pakistan. Prosthetics and orthotics international (2023)
Syeda Farwa Naqvi, Rana Muhammad Kamran Shabbir, Aslıhan Tolun, Sulman Basit, Sajid Malik
A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family. Genetic testing and molecular biomarkers 26 (1) (2022)
Khadija Murtaza, Zahra Saleem, Saliha Jabeen, A Khuzaim Alzahrani, Nadeem Kizilbash, Sajid Bashir Soofi, Haider Shirazi, Amanullah Yasin, Sajid Malik
Impact of interpregnancy intervals on perinatal and neonatal outcomes in a multiethnic Pakistani population. Journal of tropical pediatrics 68 (6) (2022)
Mine Koprulu, Muhammad Naeem, Gökhan Nalbant, Rana M Kamran Shabbir, Tariq Mahmood, Zele Huma, Sajid Malik, Aslıhan Tolun
KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies. European journal of human genetics : EJHG 30 (11) (2022)
Hafiza Fizzah Riaz, Sajid Malik
Congenital limb defects in a married female population of the Rahim Yar Khan District in Pakistan. Asian biomedicine : research, reviews and news 15 (3) (2021)
Sajid Malik, Gökhan Nalbant, Moqadsa Noreen, Muhammad Afzal, Aslıhan Tolun
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopods. American journal of medical genetics. Part A (2021)
Mine Koprulu, Aneeta Kumare, Anisa Bibi, Sajid Malik, Aslıhan Tolun
The first adolescent case of Fraser syndrome 3, with a novel nonsense variant in GRIP1. American journal of medical genetics. Part A 185 (6) (2021)
Atta Ur Rehman, Ijaz Anwar, Abdur Rashid, Sajid Malik
Frequencies of ABO and Rh (D) Blood Group Phenotypes in Pashtuns of North-Western Pakistan: A population undergoing huge demographic changes. International journal of immunogenetics 48 (4) (2021)
Rizwan Khan, Rana Muhammad Kamran Shabbir, Irum Raza, Umair Abdullah, Muhammad Asif Naeem, Ashfaque Ahmed, Sajid Malik, Zhengmao Hu, Kun Xia
A founder RDH5 splice site mutation leads to retinitis punctata albescens in two inbred Pakistani kindreds. Ophthalmic genetics 41 (1) (2020)
Esra Yıldız Bölükbaşı, Rana Muhammad Kamran Shabbir, Sajid Malik, Aslıhan Tolun
Homozygous deletion of MYADML2 in cranial asymmetry, reduced bone maturation, multiple dislocations, lumbar lordosis, and prominent clavicles. Journal of human genetics 66 (2) (2020)
Caixia Xu, Xiaoming Yang, Hang Zhou, Yongyong Li, Chao Xing, Taifeng Zhou, Dongmei Zhong, Chengjie Lian, Mei Yan, Tao Chen, Zhiheng Liao, Bo Gao, Deying Su, Tingting Wang, Swarkar Sharma, Chandra Mohan, Nadav Ahituv, Sajid Malik, Quan-Zhen Li, Peiqiang Su
A novel ZRS variant causes preaxial polydactyly type I by increased sonic hedgehog expression in the developing limb bud. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)
Yeşerin Yıldırım, Toufik Ouriachi, Ute Woehlbier, Wahiba Ouahioune, Mahmut Balkan, Sajid Malik, Aslıhan Tolun
Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility. European journal of human genetics : EJHG 26 (6) (2018)
Sajid Malik
Mesoaxial synostotic syndactyly with phalangeal reduction (MSSD): syndactyly type IX. Skeletal radiology 47 (2) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Sajid Malik