Ranad Shaheen

164PUBLICATIONS
754CO-AUTHORS
Clinical nutritionRegenerative medicine (incl. stem cells)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (164)

|Oct 14, 2026
Characterization of familial short stature with or without skeletal dysplasia in a Pakistani cohort reveals founder mutations as well as novel variants.

|Oct 12, 2026
PUS7 pseudouridylation of 7SK orchestrates human somatic cell reprogramming into iPS cells.

|Jul 29, 2026
Characterizing ARID1B-related disorders and variants of uncertain significance using DNA methylation.

|Jun 17, 2026
An Ancient Founder GDF2 Variant Potentially Causes Semi-Dominant Non-Syndromic Pulmonary Arterial Hypertension.

|Mar 30, 2026
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.

Adam Jackson, Alexander J M Blakes, Bader Alhaddad

|Dec 31, 2025
Clinical and Genetic Characterization of Hereditary Sensory and Autonomic Neuropathy Type IV in a Consanguineous Population: Identification of Novel NTRK1 Variants and Expansion of Phenotypic Spectrum.

Amal AlHashem, Hanan AlQudairy, Jana Raed

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Frequent Collaborators

17 joint publications

Henry Houlden

13 joint publications

Reza Maroofian

11 joint publications

Stephanie Efthymiou

6 joint publications

Maha S Zaki