Wasim Ahmad (W Ahmad, Wasim Ahmed, F Ahmad)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 33

Top Venues

Clinical genetics

Congenital anomalies

Clinical and experimental dermatology

Journal of human genetics

Quaid-i-Azam University Islamabad

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

Affiliation History

Quaid-i-Azam University Islamabad Jul 06 1999

Pakistan

Professor Emeritus :: Biochemistry

Publications

Fati Ullah Khan, Hammal Khan, Kifayat Ullah, Shoaib Nawaz, null Abdullah, Muhammad Javed Khan, Sohail Ahmed, Muhammad Ilyas, Amjad Ali, Imran Ullah, Aamir Sohail, Shabir Hussain, Farooq Ahmad, null Faisal, Raza Sufyan, Amir Hayat, Tooba Hanif, Fatima Bibi, Maria Hayat, Rehmat Ullah, Inam Ullah Khan, Raja Hussain Ali, Muhammad Sharif Hasni, Hamid Ali, Muhammad Bilal, Susana Peralta, Rebecca Buchert, Zamrud Zehri, Gul Hassan, Khurram Liaqat, Muhammad Zahid, Khadim Shah, Outi Mikitie, Tobias B Haack, Weizhen Ji, Saquib A Lakhani, Muhammad Ansar, Wasim Ahmad
Clinical and genetic investigation of 14 families with various forms of short stature syndromes. Clinical genetics 106 (3) (2024)
Fati Ullah Khan, Hammal Khan, Kifayat Ullah, Shoaib Nawaz, null Abdullah, Muhammad Javed Khan, Sohail Ahmed, Muhammad Ilyas, Amjad Ali, Imran Ullah, Aamir Sohail, Shabir Hussain, Farooq Ahmad, null Faisal, Raza Sufyan, Amir Hayat, Tooba Hanif, Fatima Bibi, Maria Hayat, Rehmat Ullah, Inam Ullah Khan, Raja Hussain Ali, Muhammad Sharif Hasni, Hamid Ali, Muhammad Bilal, Susana Peralta, Rebecca Buchert, Zamrud Zehri, Gul Hassan, Khurram Liaqat, Muhammad Zahid, Khadim Shah, Outi Mikitie, Tobias B Haack, Weizhen Ji, Saquib A Lakhani, Muhammad Ansar, Wasim Ahmad
Clinical and genetic investigation of 14 families with various forms of short stature syndromes. Clinical genetics (2024)
Shoaib Nawaz, Shabir Hussain, Muhammad Bilal, Najeeb Syed, Khurram Liaqat, Imran Ullah, Ammira Al-Shabeeb Akil, Khalid A Fakhro, Wasim Ahmad
A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertility. The journal of gene medicine (2023)
Warda Akbar, Asmat Ullah, Nighat Haider, Sufyan Suleman, Fati Ullah Khan, Abid Ali Shah, Muhammad Atif Sikandar, Sulman Basit, Wasim Ahmad
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia. The journal of gene medicine (2023)
Muhammad Bilal, Hammal Khan, Muhammad Javed Khan, Tobias B Haack, Rebecca Buchert, Khurram Liaqat, Kifayat Ullah, Sohail Ahmed, Thashi Bharadwaj, Anushree Acharya, Susana Peralta, null Najumuddin, Hamid Ali, Muhammad Sharif Hasni, Isabelle Schrauwen, Asmat Ullah, Wasim Ahmad, Regie Lyn P Santos-Cortez
Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly. European journal of human genetics : EJHG (2023)
Hammal Khan, Kifayat Ullah, Abid Jan, Hamid Ali, Imran Ullah, Wasim Ahmad
A variant in the LDL receptor-related protein encoding gene LRP4 underlying polydactyly and phalangeal synostosis in a family of Pakistani origin. Congenital anomalies (2023)
Hamadia Jan, Naveed Wasif, Syed Kamran-Ul-Hassan Naqvi, Imran Ullah, Wasim Ahmad
A novel homozygous splice site variant in CERS3 causes autosomal recessive congenital ichthyosis. Congenital anomalies (2023)
null Abdullah, Shabir Hussain, Weizhen Ji, Hammal Khan, Emily K Mis, Rabiha Mushtaq, Mirub Chodhary, Muhammad Hassan Raza, Abid Jan, Imran Ullah, Mustafa K Khokha, Saquib A Lakhani, Wasim Ahmad
Sequence variants in DLX5, HOXD13 and 445 kb-microduplication surrounding BTRC cause split-hand/foot malformation in three different families. Clinical genetics (2023)
Asmat Ullah, Abid Ali Shah, Majed Alluqmani, Nighat Haider, Hasan Aman, Fatima Alfadhli, Ahmed M Almatrafi, Alia M Albalawi, Jai Krishin, Fati Ullah Khan, Bilal Ali Anjam, null Abdullah, Elionora Peña Lozano, Abdus Samad, Wasim Ahmad, Torben Hansen, Kun Xia, Sulman Basit
Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 82 (8) (2022)
Rubab Raza, Asmat Ullah, Nighat Haider, Jai Krishin, Muqadar Shah, Fati Ullah Khan, null Abdullah, Torben Hansen, Syed Irfan Raza, Wasim Ahmad, Sulman Basit
Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis. Clinical and experimental dermatology (2022)
Shoaib Nawaz, Muhammad Imran Ullah, Beenish Samreen Hamid, Jalwa Nargis, Mehboob Nawaz, Shabir Hussain, Wasim Ahmad
A loss-of-function variant in DNA mismatch repair gene MLH3 underlies severe oligozoospermia. Journal of human genetics 66 (7) (2021)
Hammal Khan, Angie En Qi Chong, Muhammad Bilal, Shoaib Nawaz, null Abdullah, Sanaullah Abbasi, Amir Hussain, Shabir Hussain, Imran Ullah, Hamid Ali, Shifeng Xue, Wasim Ahmad
Novel variants in the LRP4 underlying Cenani-Lenz Syndactyly syndrome. Journal of human genetics (2021)
Samuel M Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Thashi Bharadwaj, Kevin Kum Esoh, Sulman Basit, Anushree Acharya, Liz M Nouel-Saied, Khurram Liaqat, Edmond Wonkam-Tingang, Shaheen Mowla, Gordon A Awandare, Wasim Ahmad, Regie Lyn P Santos-Cortez, Ambroise Wonkam
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of human genetics 66 (12) (2021)
Thashi Bharadwaj, Isabelle Schrauwen, Sakina Rehman, Khurram Liaqat, Anushree Acharya, Arnaud P J Giese, Liz M Nouel-Saied, Abdul Nasir, Jenna L Everard, Lana M Pollock, Shaoyuan Zhu, Michael J Bamshad, Deborah A Nickerson, Raja Hussain Ali, Asmat Ullah, Abdul Wali, Ghazanfar Ali, Regie Lyn P Santos-Cortez, Zubair M Ahmed, Brian M McDermott, Muhammad Ansar, Saima Riazuddin, Wasim Ahmad, Regie Lyn P Santos-Cortez
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment. European journal of human genetics : EJHG (2021)
Farah Bibi, Nighat Haider, Shahab Ud Din, Muqadar Shah, Jai Krishin, Naila Qayyum, Ghazala Kaukab Raja, Henry Houlden, Wasim Ahmad, Tanwir Khaliq, Asmat Ullah
Sequence variants in three genes underlying leukodystrophy in Pakistani families. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience (2020)
Asia Parveen, Muhammad Usman Mirza, Michiel Vanmeert, Javed Akhtar, Hina Bashir, Saadullah Khan, Saqib Shehzad, Matheus Froeyen, Wasim Ahmad, Muhammad Ansar, Naveed Wasif
A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations. Molecular genetics & genomic medicine 7 (9) (2019)
Muhammad Umair, Muhammad Bilal, Raja H Ali, Bader Alhaddad, Farooq Ahmad, null Abdullah, Tobias B Haack, Majid Alfadhel, Muhammad Ansar, Thomas Meitinger, Wasim Ahmad
Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limb. Clinical genetics 96 (2) (2019)
Maryam Yousaf, Asmat Ullah, Zahid Azeem, Ayesha Isani Majeed, Muhammad Iqbal Memon, Tahseen Ghous, Sulman Basit, Wasim Ahmad
Novel heterozygous sequence variant in the GLI1 underlies postaxial polydactyly. Congenital anomalies 60 (4) (2019)
Asmat Ullah, Muhammad Umair, Ayesha I Majeed, null Abdullah, Abid Jan, Wasim Ahmad
A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre-axial polydactyly. Clinical genetics 95 (4) (2019)
Shazia Khan, Siying Lin, Gaurav V Harlalka, Asmat Ullah, Khadim Shah, Sumbul Khalid, Sarmad Mehmood, Muhammad Jawad Hassan, Wasim Ahmad, Jay E Self, Andrew H Crosby, Emma L Baple, Asma Gul
BBS5 and INPP5E mutations associated with ciliopathy disorders in families from Pakistan. Annals of human genetics 83 (6) (2019)
K Shah, A Jan, F Ahmad, Sulman Basit, K Ramzan, Wasim Ahmad
Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene. Clinical and experimental dermatology 45 (2) (2019)
Farooq Ahmad, Abdul Nasir, Holger Thiele, Muhammad Umair, Guntram Borck, Wasim Ahmad
A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndrome. Annals of human genetics 82 (4) (2018)
Asmat Ullah, Muhammad Umair, Shabir Hussain, Abid Jan, Wasim Ahmad
Sequence variants in GDF5 and TRPS1 underlie brachydactyly and tricho-rhino-phalangeal syndrome type III. Pediatrics international : official journal of the Japan Pediatric Society 60 (3) (2018)
Muhammad Umair, A Ullah, S Abbas, Wasim Ahmad, Sulman Basit, W Ahmad
First direct evidence of involvement of a homozygous loss-of-function variant in the EPS15L1 gene underlying split-hand/split-foot malformation. Clinical genetics 93 (3) (2018)
Muhammad Umair, G Eckstein, G Rudolph, T Strom, E Graf, D Hendig, J Hoover, J Alanay, T Meitinger, H Schmidt, Wasim Ahmad
Homozygous XYLT2 variants as a cause of spondyloocular syndrome. Clinical genetics 93 (4) (2018)
Farooq Ahmad, Tanveer Ahmad, Muhammad Umair, null Abdullah, Wasim Ahmad
Sequence variants in the EDAR gene causing hypohidrotic ectodermal dysplasia. Congenital anomalies 59 (4) (2018)
Asmat Ullah, Muhammad Umair, Dost Muhammad, Muhammad Bilal, Kwanghyuk Lee, Suzanne M Leal, Wasim Ahmad
A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter-Thompson type. Annals of human genetics 82 (3) (2018)
F Ahmad, K Shah, M Umair, A Jan, null Irfanullah, S Khan, D Muhammad, S Basit, S M Wakil, K Ramzan, Wasim Ahmad
Novel autosomal recessive LAMA3 and PLEC variants underlie junctional epidermolysis bullosa generalized intermediate and epidermolysis bullosa simplex with muscular dystrophy in two consanguineous families. Clinical and experimental dermatology 43 (6) (2018)
Asmat Ullah, Maryam Khalid, Muhammad Umair, Sher Alam Khan, Muhammad Bilal, Saadullah Khan, Wasim Ahmad
Novel sequence variants in the MKKS gene cause Bardet-Biedl syndrome with intra- and inter-familial variable phenotypes. Congenital anomalies 58 (5) (2017)
Farooq Ahmad, Salma Sharif, Muhammad Furqan Ubaid, Khadim Shah, Muhammad Nasim Khan, Muhammad Umair, Zahid Azeem, Wasim Ahmad
Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families. Congenital anomalies 58 (1) (2017)
S Khan, M Ansar, A K Khan, K Shah, N Muhammad, S Shahzad, D A Nickerson, M J Bamshad, R L P Santos-Cortez, S M Leal, Wasim Ahmad
A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family. The British journal of dermatology 178 (2) (2017)
S Mehmood, S I Raza, H Van Bokhoven, Wasim Ahmad
Autosomal recessive transmission of a rare HOXC13 variant causes pure hair and nail ectodermal dysplasia. Clinical and experimental dermatology 42 (5) (2017)
Asmat Ullah, Muhammad Umair, Umm E-Kalsoom, Shaheen Shahzad, Sulman Basit, Wasim Ahmad
Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny. Journal of human genetics 63 (1) (2017)

Wasim Ahmad.css-eqlu8i{font-size:small;padding-left:4px;} (W Ahmad, Wasim Ahmed, F Ahmad)

Publication Activity (10 Years)

Top Topics

Top Venues

Wasim Ahmad (W Ahmad, Wasim Ahmed, F Ahmad)