Davut Pehli̇van

6.4k total citations · 1 hit paper
62 papers, 1.1k citations indexed

About

Davut Pehli̇van is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Davut Pehli̇van has authored 62 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 33 papers in Genetics and 9 papers in Cognitive Neuroscience. Recurrent topics in Davut Pehli̇van's work include Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genomics and Rare Diseases (10 papers). Davut Pehli̇van is often cited by papers focused on Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genomics and Rare Diseases (10 papers). Davut Pehli̇van collaborates with scholars based in United States, Türkiye and Kuwait. Davut Pehli̇van's co-authors include James R. Lupski, Claudia M.B. Carvalho, Richard A. Gibbs, Shalini N. Jhangiani, Ender Karaca, Zeynep Coban‐Akdemir, Donna M. Muzny, Yavuz Bayram, Ping Fang and Melissa B. Ramocki and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Nature Biotechnology.

In The Last Decade

Davut Pehli̇van

53 papers receiving 1.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Detection of mosaic and population-level structural variants with Sniffles2

2024 118 citations Moritz Smolka, Luis F. Paulin et al. Nature Biotechnology profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Davut Pehli̇van United States	17	656	508	117	102	77	62	1.1k
Eija H. Seppälä Finland	17	436 0.7×	417 0.8×	95 0.8×	29 0.3×	81 1.1×	34	1.1k
Ana Morales United States	25	1.3k 2.0×	460 0.9×	177 1.5×	43 0.4×	101 1.3×	59	2.9k
Walter Tsark United States	19	1.1k 1.6×	273 0.5×	86 0.7×	49 0.5×	151 2.0×	33	1.4k
Shuwen Huang United Kingdom	19	416 0.6×	700 1.4×	37 0.3×	125 1.2×	32 0.4×	49	997
Almuth Caliebe Germany	23	655 1.0×	678 1.3×	58 0.5×	95 0.9×	56 0.7×	66	1.4k
Carol Saunders United States	22	744 1.1×	635 1.3×	93 0.8×	26 0.3×	95 1.2×	59	1.3k
Bradford Coffee United States	18	859 1.3×	875 1.7×	79 0.7×	52 0.5×	31 0.4×	34	1.3k
Martine Doco‐Fenzy France	15	349 0.5×	302 0.6×	42 0.4×	70 0.7×	47 0.6×	29	690
Akira Kuwano Japan	19	642 1.0×	514 1.0×	260 2.2×	86 0.8×	133 1.7×	28	1.2k
Kelly Thomas United States	15	790 1.2×	962 1.9×	48 0.4×	61 0.6×	46 0.6×	22	1.6k

Countries citing papers authored by Davut Pehli̇van

Since Specialization

Citations

This map shows the geographic impact of Davut Pehli̇van's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Davut Pehli̇van with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Davut Pehli̇van more than expected).

Fields of papers citing papers by Davut Pehli̇van

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Davut Pehli̇van. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Davut Pehli̇van. The network helps show where Davut Pehli̇van may publish in the future.

Co-authorship network of co-authors of Davut Pehli̇van

This figure shows the co-authorship network connecting the top 25 collaborators of Davut Pehli̇van. A scholar is included among the top collaborators of Davut Pehli̇van based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Davut Pehli̇van. Davut Pehli̇van is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Du, Haowei, Lauren Westerfield, Yelin Wu, et al.. (2025). Expanding the Clinical and Molecular Spectrum of TUBB2B Through Distinct Variants Identified Across Multiple Families. medRxiv.

Pehli̇van, Davut, Richard A. Gibbs, Osman Uğur Sezerman, et al.. (2024). Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders. BMC Medical Genomics. 17(1). 85–85.

Smolka, Moritz, Luis F. Paulin, Christopher M. Grochowski, et al.. (2024). Detection of mosaic and population-level structural variants with Sniffles2. Nature Biotechnology. 42(10). 1571–1580. 118 indexed citations breakdown →

Bajikar, Sameer S., Yehezkel Sztainberg, Ying‐Wooi Wan, et al.. (2024). Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels. Human Molecular Genetics. 33(22). 1986–2001. 3 indexed citations

Marafi, Dana, Ruizhi Duan, Shalini N. Jhangiani, et al.. (2023). Novel LSS variants in alopecia and intellectual disability syndrome: New case report and clinical spectrum of LSS ‐related rare disease traits. Clinical Genetics. 104(3). 344–349.

Du, Haowei, Angad Jolly, Christopher M. Grochowski, et al.. (2023). HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data. Nucleic Acids Research. 52(4). e18–e18. 2 indexed citations

Cappuccio, Gerarda, Claudia M.B. Carvalho, Aleksandar Bajić, et al.. (2023). Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome. Stem Cell Research. 74. 103292–103292.

Calame, Daniel G., Tadahiro Mitani, Jawid M. Fatih, et al.. (2022). Novel RETREG1 (FAM134B) founder allele is linked to HSAN2B and renal disease in a Turkish family. American Journal of Medical Genetics Part A. 188(7). 2153–2161. 3 indexed citations

Pehli̇van, Davut, et al.. (2022). New-Onset Diabetes Presenting With Hyperosmolar Hyperglycemic State in a Lean Adolescent With Atypical Rett Syndrome Using Antipsychotics. Clinical Diabetes. 40(4). 503–507. 1 indexed citations

10.

Aktürk, Zekeriya, et al.. (2022). Assessing the Burden on Caregivers of MECP2 Duplication Syndrome. Pediatric Neurology. 133. 1–8. 6 indexed citations

11.

Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant. Annals of Clinical and Translational Neurology. 8(10). 2052–2058.

12.

Herman, Isabella, Angad Jolly, Haowei Du, et al.. (2021). Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses. American Journal of Medical Genetics Part A. 188(3). 735–750. 7 indexed citations

13.

Calame, Daniel G., Jawid M. Fatih, Isabella Herman, et al.. (2021). Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy. Neurology Genetics. 7(3). e589–e589. 9 indexed citations

14.

Karakas, Cemal, et al.. (2019). Clinical Presentation, Neuroimaging Characteristics and Long-term Outcome in Pediatric Cerebral Venous Sinus Thrombosis: A Retrospective Study (P2.3-052). Neurology. 92(15_supplement).

15.

Bayram, Yavuz, Hatip Aydın, Tomasz Gambin, et al.. (2015). Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral‐facial‐digital syndrome type VI. American Journal of Medical Genetics Part A. 167(9). 2132–2137. 9 indexed citations

16.

Karaca, Ender, Ramazan Büyükkaya, Davut Pehli̇van, et al.. (2014). Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome. The Journal of Clinical Endocrinology & Metabolism. 100(1). E140–E147. 60 indexed citations

17.

Okamoto, Yuji, Davut Pehli̇van, Christine R. Beck, et al.. (2013). Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D. Genetics in Medicine. 16(5). 386–394. 29 indexed citations

18.

Gündüz, Mehmet, Esra Gündüz, Levent Beder, et al.. (2012). Metastasis: Genetics, Mechanism, and Diagnostic and Therapeutic Strategies. Journal of Oncology. 2012. 1–2. 2 indexed citations

19.

Pehli̇van, Davut, Melanie Hullings, Claudia M.B. Carvalho, et al.. (2012). NIPBL rearrangements in Cornelia de Lange syndrome: evidence for replicative mechanism and genotype–phenotype correlation. Genetics in Medicine. 14(3). 313–322. 18 indexed citations

20.

Gündüz, Mehmet, Levent Beder, Esra Gündüz, et al.. (2008). Downregulation of ING3 mRNA expression predicts poor prognosis in head and neck cancer. Cancer Science. 99(3). 531–538. 46 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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