Zeynep Tümer

11.7k total citations · 2 hit papers
180 papers, 5.7k citations indexed

About

Zeynep Tümer is a scholar working on Molecular Biology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, Zeynep Tümer has authored 180 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 104 papers in Molecular Biology, 95 papers in Genetics and 33 papers in Nutrition and Dietetics. Recurrent topics in Zeynep Tümer's work include Genomic variations and chromosomal abnormalities (49 papers), Trace Elements in Health (33 papers) and Genetics and Neurodevelopmental Disorders (32 papers). Zeynep Tümer is often cited by papers focused on Genomic variations and chromosomal abnormalities (49 papers), Trace Elements in Health (33 papers) and Genetics and Neurodevelopmental Disorders (32 papers). Zeynep Tümer collaborates with scholars based in Denmark, Germany and United Kingdom. Zeynep Tümer's co-authors include Niels Tommerup, Nina Horn, Lisbeth Birk Møller, T. Tønnesen, Daniella Bach‐Holm, Karen Brøndum‐Nielsen, Anthony P. Monaco, Jamel Chelly, Yumiko Ishikawa-Brush and Yves Moreau and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Nature Biotechnology.

In The Last Decade

Zeynep Tümer

178 papers receiving 5.6k citations

Hit Papers

align trajectories sort by overperformance

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.

A human phenome-interactome network of protein complexes implicated in genetic disorders

2007 659 citations Zeynep Tümer, Niels Tommerup et al. profile →
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

1993 557 citations Zeynep Tümer, Niels Tommerup et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Zeynep Tümer	3.4k	1.9k	1.5k	517	497	180	5.7k
Paul J. Lockhart	2.3k 0.7×	820 0.4×	1.5k 1.0×	201 0.4×	712 1.4×	126	5.2k
Massimo Carella	2.9k 0.9×	1.1k 0.6×	1.1k 0.7×	420 0.8×	65 0.1×	225	6.1k
Kevin P. Rosenblatt	4.1k 1.2×	2.3k 1.2×	648 0.4×	255 0.5×	28 0.1×	78	8.5k
Rosalba Carrozzo	4.0k 1.2×	845 0.4×	185 0.1×	255 0.5×	47 0.1×	143	5.3k
Carol Nelson‐Williams	6.8k 2.0×	1.7k 0.9×	1.2k 0.8×	314 0.6×	11 0.0×	56	10.4k
Adrian Clark	3.5k 1.0×	1.7k 0.9×	866 0.6×	737 1.4×	34 0.1×	137	8.2k
Norman S. Wolf	2.5k 0.7×	272 0.1×	159 0.1×	188 0.4×	126 0.3×	67	5.2k
Bruce D. Weintraub	2.5k 0.7×	1.4k 0.7×	240 0.2×	331 0.6×	74 0.1×	166	8.6k
Richard I. Kelley	7.4k 2.2×	1.8k 0.9×	181 0.1×	663 1.3×	26 0.1×	143	10.1k
Brian J. Feldman	2.2k 0.7×	753 0.4×	269 0.2×	103 0.2×	48 0.1×	46	5.2k

Countries citing papers authored by Zeynep Tümer

Since Specialization

Citations

This map shows the geographic impact of Zeynep Tümer'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 Zeynep Tümer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zeynep Tümer more than expected).

Fields of papers citing papers by Zeynep Tümer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zeynep Tümer. 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 Zeynep Tümer. The network helps show where Zeynep Tümer may publish in the future.

Co-authorship network of co-authors of Zeynep Tümer

This figure shows the co-authorship network connecting the top 25 collaborators of Zeynep Tümer. A scholar is included among the top collaborators of Zeynep Tümer 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 Zeynep Tümer. Zeynep Tümer 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

Stödberg, Tommy, Malin Kvarnung, Katrina Tatton‐Brown, et al.. (2024). Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variant. Clinical Genetics. 106(4). 427–436. 1 indexed citations

Hjortshøj, Tina Duelund, Morten Dunø, Lotte Risom, et al.. (2023). DNA methylation signature classification of rare disorders using publicly available methylation data. Clinical Genetics. 103(6). 688–692. 1 indexed citations

Johannesen, Katrine M., Zeynep Tümer, Sarah Weckhuysen, Tahsin Stefan Barakat, & Allan Bayat. (2023). Solving the unsolved genetic epilepsies: Current and future perspectives. Epilepsia. 64(12). 3143–3154. 8 indexed citations

Gómez‐Puertas, Paulino, et al.. (2022). Neurodevelopmental Disorders Associated with PSD-95 and Its Interaction Partners. International Journal of Molecular Sciences. 23(8). 4390–4390. 48 indexed citations

Schönewolf‐Greulich, Bitten, Alexandra Afenjar, Magalie Barth, et al.. (2021). Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders. Clinical Genetics. 100(5). 628–633. 26 indexed citations

Hjortshøj, Tina Duelund, A.R. Sørensen, Bo Mølholm Hansen, et al.. (2020). upd(20)mat is a rare cause of the Silver‐Russell‐syndrome‐like phenotype: Two unrelated cases and screening of large cohorts. Clinical Genetics. 97(6). 902–907. 9 indexed citations

Gallagher, Louise, Severin Rakić, Paula Jorge, et al.. (2020). Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature. International Journal of Environmental Research and Public Health. 17(24). 9253–9253. 4 indexed citations

Bayat, Allan, Katrine M. Johannesen, Tahsin Stefan Barakat, et al.. (2020). Deciphering the premature mortality in PIGA-CDG – An untold story. Epilepsy Research. 170. 106530–106530. 17 indexed citations

Eggermann, Thomas, Guiomar Pérez de Nanclares, Eamonn R. Maher, et al.. (2015). Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Clinical Epigenetics. 7(1). 123–123. 130 indexed citations

10.

Bertelsen, Birgitte, Lusine Nazaryan‐Petersen, Wei Sun, et al.. (2015). A germline chromothripsis event stably segregating in 11 individuals through three generations. Genetics in Medicine. 18(5). 494–500. 54 indexed citations

11.

Bertelsen, Birgitte, Linea Cecilie Melchior, Lars R. Jensen, et al.. (2014). A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD. Psychiatry Research. 225(3). 268–275. 13 indexed citations

12.

Grønskov, Karen, et al.. (2014). Mosaicism for c.431_454dup in ARX causes a mild Partington syndrome phenotype. European Journal of Medical Genetics. 57(6). 284–287. 4 indexed citations

13.

Bertelsen, Birgitte, Nanette Mol Debes, Liselotte Skov, et al.. (2013). Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 825–831. 26 indexed citations

14.

Møller, Lisbeth Birk, Małgorzata Lenartowicz, M. T. Zabot, et al.. (2012). Clinical expression of Menkes disease in females with normal karyotype. Orphanet Journal of Rare Diseases. 7(1). 6–6. 36 indexed citations

15.

Lind-Thomsen, Allan, Mikkel W. Pedersen, Hanne Jarmer, et al.. (2008). GLI1 Is Involved in Cell Cycle Regulation and Proliferation of NT2 Embryonal Carcinoma Stem Cells. DNA and Cell Biology. 27(5). 251–256. 9 indexed citations

16.

Møller, Rikke S., Maria Hoeltzenbein, Babett Heye, et al.. (2008). Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly. The American Journal of Human Genetics. 82(5). 1165–1170. 116 indexed citations

17.

Zhang, Litu, et al.. (2006). Screening of 99 Danish Patients with Congenital Heart Disease for GATA4 Mutations. Genetic Testing. 10(4). 277–280. 18 indexed citations

18.

Tümer, Zeynep, et al.. (2004). Identification of a Novel EYA1 Splice-Site Mutation in a Danish Branchio-Oto-Renal Syndrome Family. Genetic Testing. 8(4). 404–406. 7 indexed citations

19.

Møller, Lisbeth Birk, et al.. (2004). X-Linked Menkes Disease: First Documented Report of Germ-Line Mosaicism. Genetic Testing. 8(3). 286–291. 6 indexed citations

20.

Poulsen, Louise Ladefoged, et al.. (2002). X‐linked recessive Menkes disease: identification of partial gene deletions in affected males. Clinical Genetics. 62(6). 449–457. 17 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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