Concepedia

Farid Ullah

FU

Statistics

Publications

9

Citations

763

H-Index

9

Active since

2017

Affiliations

National Institute for Biotechnology and Genetic Engineering(Current)

Pakistan Institute of Engineering and Applied Sciences

Lurie Children's Hospital

Northwestern University

University of Cologne

Farid Ullah is an author at National Institute for Biotechnology and Genetic Engineering specializing in genetics, life sciences, and molecular genetics.

ORCID

Publications per year

2017–2022

9

Publications

9

A cross-disorder dosage sensitivity map of the human genome

Ryan L. Collins, Joseph Glessner, Eleonora Porcu et al. · Cell · 2022 · 360 citations · Full text

, , +7

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder

Valentina Del Dotto, Farid Ullah, Ivano Di Meo et al. · Journal of Clinical Investigation · 2019 · 92 citations · Full text

, , +17

Mutations of <i>KIF14</i> cause primary microcephaly by impairing cytokinesis

Abubakar Moawia, Ranad Shaheen, Sajida Rasool et al. · Annals of Neurology · 2017 · 85 citations

, , +17

A cross-disorder dosage sensitivity map of the human genome

Ryan L. Collins, Joseph Glessner, Eleonora Porcu et al. · medRxiv · 2021 · 54 citations · Full text

, , +7

Biallelic variants in <i>LIG3</i> cause a novel mitochondrial neurogastrointestinal encephalomyopathy

Elena Bonora, Sanjiban Chakrabarty, Georgios Kellaris et al. · Brain · 2021 · 42 citations · Full text

, , +17

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