Zafar Iqbal (Z Iqbal)

ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 9

Top Venues

Molecular genetics and genomics : MGG

Genes

Nature genetics

European journal of human genetics : EJHG

Oslo universitetssykehus Rikshospitalet

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

Affiliation History

Oslo universitetssykehus Rikshospitalet Jan 01 2017

Norway

Researcher :: Neurology

Publications

Tehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti, Zaineb Akram, Imran Khan Yousafzai, Wajahat Bin Naeem, Nasreen Fatima, Asmat Ali, Zafar Iqbal, Ayaz Khan, Muhammad Shahzad, Chunyu Liu, Mathias Toft, Feng Zhang, Muhammad Tariq, Erica E Davis, Tahir N Khan
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN. Molecular genetics and genomics : MGG 299 (1) (2024)
Tehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti, Zaineb Akram, Imran Khan Yousafzai, Wajahat Bin Naeem, Nasreen Fatima, Asmat Ali, Zafar Iqbal, Ayaz Khan, Muhammad Shahzad, Chunyu Liu, Mathias Toft, Feng Zhang, Muhammad Tariq, Erica E Davis, Tahir N Khan
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN. Molecular genetics and genomics : MGG 299 (1) (2024)
Saadia Maryam Saadi, Elisa Cali, Lubaba Bintee Khalid, Hammad Yousaf, Ghazala Zafar, Haq Nawaz Khan, Muhammad Sher, Barbara Vona, Uzma Abdullah, Naveed Altaf Malik, Joakim Klar, Stephanie Efthymiou, Niklas Dahl, Henry Houlden, Mathias Toft, Shahid Mahmood Baig, Ambrin Fatima, Zafar Iqbal
Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders. Genes 14 (7) (2023)
Hammad Yousaf, Ambrin Fatima, Zafar Ali, Shahid M Baig, Mathias Toft, Zafar Iqbal
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family. Genes 13 (9) (2022)
Zafar Iqbal, Mathias Toft
TMEM230 variants in Parkinson's disease. Nature genetics 51 (3) (2019)
Zafar Iqbal, Jeanette Koht, Lasse Pihlstrom, Sandra P Henriksen, Chiara Cappelletti, Michael Bjørn Russel, Osmar Norberto de Souza, Inger Marie Skogseid, Mathias Toft
Missense mutations in DYT-TOR1A dystonia. Neurology. Genetics 5 (4) (2019)
Zafar Iqbal, Siri L Rydning, Iselin M Wedding, Jeanette Koht, Lasse Pihlstrøm, Aina H Rengmark, Sandra P Henriksen, Chantal M E Tallaksen, Mathias Toft
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia. PloS one 12 (3) (2017)
S Riazuddin, M Hussain, A Razzaq, Zafar Iqbal, M Shahzad, D L Polla, Y Song, E van Beusekom, A A Khan, L Tomas-Roca, M Rashid, M Y Zahoor, W M Wissink-Lindhout, M A R Basra, M Ansar, Z Agha, K van Heeswijk, F Rasheed, M Van de Vorst, J A Veltman, Christian Gilissen, J Akram, T Kleefstra, M Z Assir, null null, D Grozeva, K Carss, F L Raymond, T D O'Connor, S A Riazuddin, S N Khan, Z M Ahmed, A P M de Brouwer, H van Bokhoven, S Riazuddin
Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability. Molecular psychiatry 22 (11) (2016)
Zafar Iqbal, Lucia Püttmann, Luciana Musante, Attia Razzaq, Muhammad Yasir Zahoor, Hao Hu, Thomas F Wienker, Masoud Garshasbi, Zohreh Fattahi, Christian Gilissen, Lisenka E L M Vissers, Arjan P M de Brouwer, Joris A Veltman, Rolph Pfundt, Hossein Najmabadi, Hans-Hilger Ropers, Sheikh Riazuddin, Kimia Kahrizi, Hans van Bokhoven
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration. European journal of human genetics : EJHG 24 (3) (2015)

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Publication Activity (10 Years)

Top Topics

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Zafar Iqbal (Z Iqbal)