Zafar Iqbal

9PUBLICATIONS
22CO-AUTHORS
Psychosocial aspects of childbirth and perinatal mental healthNeurology and neuromuscular diseasesGene mappingMedical parasitologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|Jun 20, 2025
Evidence That Dmrta2 Acts through Repression of Pax6 in Cortical Patterning and Identification of a Mutation Impairing DNA Recognition Associated with Microcephaly in Human.

Xueyi Shen, Jithu Anirudhan, Ambrin Fatima

|May 21, 2024
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN.

Tehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti

|Jul 29, 2023
Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Saadia Maryam Saadi, Elisa Cali, Lubaba Bintee Khalid

|Sep 23, 2022
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family.

Hammad Yousaf, Ambrin Fatima, Zafar Ali

|Jul 20, 2019
Missense mutations in DYT-TOR1A dystonia.

Zafar Iqbal, Jeanette Koht, Lasse Pihlstrøm

|Feb 27, 2019
TMEM230 variants in Parkinson's disease.

Zafar Iqbal, Mathias Toft

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Frequent Collaborators

3 joint publications

Mathias Toft

1 joint publications

C Gilissen

1 joint publications

Lasse Pihlstrøm

1 joint publications

Zafar Ali