Kamran Salayev

Also affiliated with Azerbaijan Medical University

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations”.

PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations

Clinical Genetics(2020)10.1111/cge.13877

N/A

0DataRank · unranked

11 citations

Rauan Kaiyrzhanov, Reza Maroofian, Thi Tuyet Mai Nguyen, Kamran Salayev, Ilana Chilton +7 more

Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals

Genetics in Medicine(2022)10.1016/j.gim.2022.09.010

N/A

0DataRank · unranked

39 citations

Reza Maroofian, Toru Sengoku, Tadahiro Mitani, Alistair T. Pagnamenta, Dana Marafi +82 more

Assessment of Research Ethics Knowledge of Pediatricians in Azerbaijan

Research Square(2022)10.21203/rs.3.rs-2416689/v1

N/A

0DataRank · unranked

0 citations

Ulviyya Aslanova, Narmin Guliyeva, Geray Geraybeyli, Kerim Münir, Kamran Salayev

Attitudes of Parents of Children with Rare Neurological Disorders Toward Clinical Genetic Testing

Research Square(2023)10.21203/rs.3.rs-3266696/v1

N/A

0DataRank · unranked

0 citations

Ulviyya Guliyeva, Sugra Guliyeva, Rauan Kaiyrzhanov, Ulviyya Aslanova, Narmin Guliyeva +3 more

Assessment of Research Ethics Knowledge of Pediatricians

Global Pediatric Health(2024)10.1177/2333794x231224989

N/A

0DataRank · unranked

1 citations

Ulviyya Aslanova, Narmin Guliyeva, Geray Geraybeyli, Kerim Münir, Kamran Salayev

Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.018

N/A

0DataRank · unranked

6 citations

Laura Harrold, Daniel G. Calame, Claire Salter, Takashi Kikuma, Kevin P. Guay +49 more

SLK is mutated in individuals with a neurodevelopmental disorder

EBioMedicine(2025)10.1016/j.ebiom.2025.105725

N/A

0DataRank · unranked

2 citations

Norah Altuwaijri, Jun‐yi Zhu, Stéphanie Efthymiou, Hangnoh Lee, Jianli Duan +94 more

A CGG Repeat Expansion in CSNK1E Associated with Progressive Myoclonic Epilepsy with Incomplete Penetrance

Movement Disorders(2025)10.1002/mds.30326

N/A

0DataRank · unranked

0 citations

Pilar Álvarez Jerez, Ulviyya Guliyeva, Jasmine Lee, Laksh Malik, Breeana Baker +9 more

Consanguinity and treatment strategy determine seizure outcome and mortality in infantile epileptic spasms syndrome in Azerbaijan

Seizure(2025)10.1016/j.seizure.2025.09.001

N/A

0DataRank · unranked

0 citations

Nana Nino Tatishvili, Kamran Salayev, Rauan Kaiyrzhanov, Semra Hız, Kerim Münir +6 more