Yalda Jamshidi

22PUBLICATIONS
241CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Anthropological geneticsNeurology and neuromuscular diseasesMedical biochemistry - lipidsCell and nuclear division
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Publications (22)

|Jun 04, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.

|Mar 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Hye In Kim, Christopher DeBoever, Klaudia Walter

|Sep 26, 2025
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics.

Gregorio A Nolasco, Mònica Roldán, Yalda Jamshidi

|Nov 11, 2023
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.

Rauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin

|Jan 21, 2023
Genetic Insights from Consanguineous Cardiomyopathy Families.

Constance Maurer, Olga Boleti, Paria Najarzadeh Torbati

|Dec 19, 2022
Correction to: Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'.

Francesca Forzano, Olga Antonova, Angus Clarke

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Frequent Collaborators

5 joint publications

Francesca Forzano

5 joint publications

Maurizio Genuardi

5 joint publications

Alexandre Reymond

5 joint publications

Angus Clarke