Concepedia

Kolsoum Saeidi

KS

Statistics

Publications

8

Citations

238

H-Index

8

Active since

2014

Affiliations

Kerman University of Medical Sciences(Current)

Children’s Institute

Istituti di Ricovero e Cura a Carattere Scientifico

University College London

National Hospital for Neurology and Neurosurgery

Kolsoum Saeidi is an author at Kerman University of Medical Sciences specializing in genetics, molecular genetics, and neurogenetic disorders.

ORCID

Publications per year

2014–2022

8

Publications

8

Genotype-phenotype correlation in Pompe disease, a step forward

Paola De Filippi, Kolsoum Saeidi, Sabrina Ravaglia et al. · Orphanet Journal of Rare Diseases · 2014 · 66 citations · Full text

, , +17

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive <i>c</i>erebellar, <i>o</i>cular, cranio<i>f</i>acial and <i>g</i>enital features (COFG syndrome)

Abolfazl Rad, Umut Altunoğlu, Rebecca Miller et al. · Journal of Medical Genetics · 2018 · 38 citations · Full text

, , +17

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

Zheng Yie Yap, Stéphanie Efthymiou, Simone Seiffert et al. · The American Journal of Human Genetics · 2021 · 32 citations · Full text

, , +14

Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish

Barbara Vona, Patrícia Gonçalves Barbalho, Rauan Kaiyrzhanov et al. · Genetics in Medicine · 2021 · 31 citations · Full text

, , +13

Quantification of circulating miR-517c-3p and miR-210-3p levels in preeclampsia

Reza Molla Ali-Nejad, Kolsoum Saeidi, Sedigheh Gharbi et al. · Pregnancy Hypertension · 2019 · 25 citations

, , +11

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