Sehime Gulsun Temel

Biochemistry, Genetics and Molecular BiologyMedicine

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 8 papers. Top paper: “ACMG-Recommended Actionable Secondary Findings from 1600 Clinical Exomes in the South Marmara Region in Turkiye”.

ACMG-Recommended Actionable Secondary Findings from 1600 Clinical Exomes in the South Marmara Region in Turkiye

International Journal of Molecular Sciences(2026)10.3390/ijms27031491

N/A

0DataRank · unranked

0 citations

Mustafa Samet Pir, Cuneyd Yavas, Feride I. Sahin, Sebnem Ozemri Sag, Yunus Kasim Terzi +3 more

Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.010

N/A

0DataRank · unranked

105 citations

Sehime Gulsun Temel, Liina Nagirnaja, Manon S. Oud, Alexandra M. Lopes, Godfried W. van der Heijden +29 more

Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.11.010

N/A

0DataRank · unranked

41 citations

Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Saleh Al‐Muhsen, Fahd Al‐Mulla +63 more

Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2023.02.003

N/A

0DataRank · unranked

16 citations

Laurent Abel, Salah Al-Muhsen, Alessandro Aiuti, Fahd Al‐Mulla, Evangelos Andreakos +70 more

SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency

The Journal of Experimental Medicine(2024)10.1084/jem.20231725

N/A

0DataRank · unranked

20 citations

Vanja Lundberg, Jérémie Le Pen, Jiayi Yuan, Danyel Lee, Francesca Pinci +94 more

A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity

The Journal of Experimental Medicine(2024)10.1084/jem.20241413

N/A

0DataRank · unranked

13 citations

Jérémie Le Pen, Nicole A. de Weerd, Marcela Moncada‐Vélez, Marie Materna, Daniel Chieh-Ding Lin +89 more

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

Life Science Alliance(2024)10.26508/lsa.202402708

N/A

0DataRank · unranked

6 citations

Irmak Sakin, Stephen Viviano, Gülten Tuncel, Stephanie Marie Aguilera, Gizem Goles +15 more

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma

Genetics in Medicine(2024)10.1016/j.gim.2024.101125

N/A

0DataRank · unranked

3 citations

Mythily Ganapathi, Yiming Zheng, Kai-Li Tan, Oguz Kanca, Kevin E. Bove +21 more