Kaya Bilgüvar

Also affiliated with Acıbadem University, Yale University, Kent Hastanesi, Pediatrics and Genetics, Acıbadem Adana Hospital

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 2%percentile

2.4Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

The genetic structure of the Turkish population reveals high levels of variation and admixture

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2026076118

Top 9%

2.4DataRank

Top 9%98 citations

A. Nazlı Başak, Onur Emre Onat, Kaya Bilgüvar, Jungmin Choi, Yuval Itan +11 more

Papers

Driven by 25 papers — median percentile 91. Top paper: “Inborn errors of type I IFN immunity in patients with life-threatening COVID-19”.

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Science(2020)10.1126/science.abd4570

N/A

5.6DataRank · unranked

2400 citations

Paul Bastard, Zhiyong Liu, Jérémie Le Pen, Marcela Moncada‐Vélez, Jie Chen +95 more

The genetic structure of the Turkish population reveals high levels of variation and admixture

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2026076118

Top 9%

2.4DataRank

Top 9%98 citations

A. Nazlı Başak, Onur Emre Onat, Kaya Bilgüvar, Jungmin Choi, Yuval Itan +11 more

Autoantibodies against type I IFNs in patients with life-threatening COVID-19

Science(2020)10.1126/science.abd4585

N/A

1.2DataRank · unranked

2821 citations

Lindsey B. Rosen, Qian Zhang, Eleftherios Michailidis, Hans-Heinrich Hoffmann, Yu Zhang +95 more

Neuroinvasion of SARS-CoV-2 in human and mouse brain

The Journal of Experimental Medicine(2020)10.1084/jem.20202135

N/A

1.0DataRank · unranked

1028 citations

Ce Zhang, Benjamin Israelow, Alice Lu-Culligan, Alba Vieites‐Prado, Sophie Skriabine +34 more

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

The American Journal of Human Genetics(2015)10.1016/j.ajhg.2015.06.009

N/A

0.980DataRank · unranked

687 citations

Kati J. Buckingham, Shalini N. Jhangiani, Corinne Boehm, Nara Sobreira, Joshua D. Smith +46 more

Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.662903

N/A

0DataRank · unranked

78 citations

Shoaib Nawaz, Jungmin Choi, Huafeng Wang, Shabir Hussain, Mehboob Nawaz +12 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

ALG13 X‐linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes

Journal of Inherited Metabolic Disease(2021)10.1002/jimd.12378

N/A

0DataRank · unranked

29 citations

Miao He, Andrew C. Edmondson, Earnest James Paul Daniel, Jie Chen, Tyhiesia Donald +21 more

Mutation in ZDHHC15 Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual Disability

Neurology Genetics(2021)10.1212/nxg.0000000000000602

N/A

0DataRank · unranked

11 citations

Somayeh Bakhtiari, Jennifer Heim, Patricia Cornejo, James Liu, Aris J. Huang +6 more

Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy

Neurology Genetics(2021)10.1212/nxg.0000000000000583

N/A

0DataRank · unranked

8 citations

Abbas Tafakhori, Sheng Chih Jin, Brandon S. Guida, Elham Alehabib, Saghar Firouzbadi +5 more

Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

Science(2022)10.1126/science.abo3627

N/A

0DataRank · unranked

168 citations

Jérémie Le Pen, Ahmad Yatim, Beihua Dong, Yann Aquino, Masato Ogishi +95 more

Lineage abundance estimation for SARS-CoV-2 in wastewater using transcriptome quantification techniques

Genome biology(2022)10.1186/s13059-022-02805-9

N/A

0DataRank · unranked

55 citations

Alessandro Zulli, Isabel M. Ott, Ioanna Nika, Mart J. van der Lugt, Mary E. Petrone +48 more

Mutation spectrum of congenital heart disease in a consanguineous Turkish population

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1944

N/A

0DataRank · unranked

13 citations

Hande Kaymakçalan, Sheng Chih Jin, Nicholas S. Diab, İbrahim Cansaran Tanıdır, Ali Seyfi Yalım Yalçın +7 more

Application of multiplex amplicon deep-sequencing (MAD-seq) to screen for putative drug resistance markers in the Necator americanus isotype-1 β-tubulin gene

Scientific Reports(2022)10.1038/s41598-022-15718-1

N/A

0DataRank · unranked

11 citations

Peter Suwondo, Jewelna Akorli, Joseph Otchere, Lisa M. Harrison, Kaya Bilgüvar +6 more

Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2214997120

N/A

0DataRank · unranked

20 citations

Tanyeri Barak, Leon D. Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera +25 more

Super-enhancer hijacking drives ectopic expression of hedgehog pathway ligands in meningiomas

Nature Communications(2023)10.1038/s41467-023-41926-y

N/A

0DataRank · unranked

19 citations

E. Zeynep Erson‐Omay, Chang Li, Hinda Najem, Süleyman Coşkun, Evgeniya Tyrtova +32 more

LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertility

eLife(2023)10.7554/elife.90095

N/A

0DataRank · unranked

9 citations

Pengxin Chai, Shoaib Nawaz, Jungmin Choi, Francesc López‐Giráldez, Shabir Hussain +7 more

LRRC23 truncation impairs radial spoke 3 head assembly and sperm motility underlying male infertility

eLife(2023)10.7554/elife.90095.3

N/A

0DataRank · unranked

8 citations

Pengxin Chai, Shoaib Nawaz, Jungmin Choi, Francesc López‐Giráldez, Shabir Hussain +7 more

TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions

Brain(2023)10.1093/brain/awad301

N/A

0DataRank · unranked

7 citations

Sara A. Lewis, Somayeh Bakhtiari, Sandra H. Nordlie, Alex M. Pagnozzi, Helen Magee +55 more

Novel PIBF1 Pathogenic Variant in Three Siblings with Joubert Syndrome Type 33

Molecular Syndromology(2024)10.1159/000543107

N/A

0DataRank · unranked

1 citations

Bahadır M. Samur, Ummu Gulsum Ozgul Gumus, Kaya Bilgüvar, Ayten Güleç, Stéphanie Efthymiou +4 more

Dysregulation of mTOR signalling is a converging mechanism in lissencephaly

Nature(2025)10.1038/s41586-024-08341-9

N/A

0DataRank · unranked

20 citations

Dan Liang, A. Gulhan Ercan‐Sencicek, A Bulut, Jason Cortés, Iris Q. Cheng +27 more

Human CRY1 variants associate with attention deficit/hyperactivity disorder

Journal of Clinical Investigation(2020)10.1172/jci135500

N/A

0DataRank · unranked

47 citations

Meltem Ece Kars, Şeref Gül, Kaya Bilgüvar, Yiming Wu, Ayşe Özhan +13 more

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Brain(2020)10.1093/brain/awaa085

N/A

0DataRank · unranked

32 citations

Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tüysüz +40 more

METAP1 mutation is a novel candidate for autosomal recessive intellectual disability

Journal of Human Genetics(2020)10.1038/s10038-020-0820-0

N/A

0DataRank · unranked

2 citations

Fesih Aktar, Kaya Bilgüvar, Jacob F. Baranoski, Gozde Akgumus, Akdes Serin Harmancı +5 more

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

Science Immunology(2021)10.1126/sciimmunol.abl4348

N/A

0DataRank · unranked

421 citations

Bertrand Boisson, Fanny Onodi, Daniela Matuozzo, Marcela Moncada‐Vélez, Majistor Raj Luxman Maglorius Renkilaraj +95 more

Kaya Bilgüvar

Indexed papers

Top data-sharing exemplar

Papers