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

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 →

Peers

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

#	Work	Indexed citations
1	Unraveling GRIA1 neurodevelopmental disorders: Lessons learned from the p.(Ala636Thr) variant 2024 ·Clinical Genetics ·(unknown), (unknown), Tommy Stödberg, Malin Kvarnung, Katrina Tatton‐Brown, Diana Baralle, Zeynep Tümer, Allan Bayat	1
2	DNA methylation signature classification of rare disorders using publicly available methylation data 2023 ·Clinical Genetics ·(unknown), (unknown), Tina Duelund Hjortshøj, Morten Dunø, Lotte Risom, Mads Bak, Jakob Ek, Rikke S. Møller, Andrea Ciolfi, Marco Tartaglia, Zeynep Tümer	1
3	Solving the unsolved genetic epilepsies: Current and future perspectives 2023 ·Epilepsia ·Katrine M. Johannesen, Zeynep Tümer, Sarah Weckhuysen, Tahsin Stefan Barakat, Allan Bayat	8
4	Neurodevelopmental Disorders Associated with PSD-95 and Its Interaction Partners 2022 ·International Journal of Molecular Sciences ·(unknown), Paulino Gómez‐Puertas, Zeynep Tümer	48
5	Clinical and molecular delineation of PUS3 ‐associated neurodevelopmental disorders 2021 ·Clinical Genetics ·(unknown), (unknown), Bitten Schönewolf‐Greulich, Alexandra Afenjar, Magalie Barth, Felix Boschann, Diane Doummar, Tobias B. Haack, Boris Keren, Л. А. Лившиц, Davide Mei, Joohyun Park, Tiziana Pisano, (unknown), Muhammad Umair, Ahmed Waqas, Alban Ziegler, Renzo Guerrini, Rikke S. Møller, Zeynep Tümer	26
6	upd(20)mat is a rare cause of the Silver‐Russell‐syndrome‐like phenotype: Two unrelated cases and screening of large cohorts 2020 ·Clinical Genetics ·Tina Duelund Hjortshøj, A.R. Sørensen, (unknown), Bo Mølholm Hansen, Morten Dunø, Marie Balslev‐Harder, Karen Grønskov, Johanna M. van Hagen, Abeltje M. Polstra, Thomas Eggermann, Martijn J.J. Finken, Zeynep Tümer	9
7	Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature 2020 ·International Journal of Environmental Research and Public Health ·(unknown), (unknown), Louise Gallagher, Severin Rakić, Paula Jorge, Goran Čuturilo, Silvana Markovska-Simoska, Isabella Borg, Jeanne Wolstencroft, Zeynep Tümer, Adrian J. Harwood, Yllka Kodra, David Skuse	4
8	Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci 2015 ·Clinical Epigenetics ·Thomas Eggermann, Guiomar Pérez de Nanclares, Eamonn R. Maher, I. Karen Temple, Zeynep Tümer, David Monk, Deborah Mackay, Karen Grønskov, Andrea Riccio, Agnès Linglart, Irène Netchine	130
9	A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD 2014 ·Psychiatry Research ·Birgitte Bertelsen, Linea Cecilie Melchior, Lars R. Jensen, (unknown), (unknown), Nanette Mol Debes, Liselotte Skov, Gangcai Xie, Wei Sun, Karen Brøndum‐Nielsen, Andreas W. Kuß, Wei Chen, Zeynep Tümer	13
10	Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities 2013 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown), Birgitte Bertelsen, Nanette Mol Debes, (unknown), Liselotte Skov, Jens D. Mikkelsen, Karen Brøndum‐Nielsen, Zeynep Tümer	26
11	Clinical expression of Menkes disease in females with normal karyotype 2012 ·Orphanet Journal of Rare Diseases ·Lisbeth Birk Møller, Małgorzata Lenartowicz, M. T. Zabot, Josiane Arnaud, Lydie Bürglen, Chris Bennett, (unknown), Richard Fisher, Sandra Janssens, Shehla Mohammed, Margreet G.E.M. Ausems, Zeynep Tümer, Nina Horn, Thomas G. Jensen	36
12	Three New Loci for Determining X Chromosome Inactivation Patterns 2011 ·Journal of Molecular Diagnostics ·Birgitte Bertelsen, Zeynep Tümer, Kirstine Ravn	37
13	Clinical utility gene card for: Menkes disease 2011 ·European Journal of Human Genetics ·Zeynep Tümer, Leo W. J. Klomp	1
14	Interstitial deletion of 14q24.3‐q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects 2010 ·American Journal of Medical Genetics Part A ·Sultan Cingöz, Iben Bache, (unknown), Hans‐Hilger Ropers, Niels Tommerup, Hanne Jensen, (unknown), Zeynep Tümer	6
15	GLI1 Is Involved in Cell Cycle Regulation and Proliferation of NT2 Embryonal Carcinoma Stem Cells 2008 ·DNA and Cell Biology ·(unknown), Allan Lind-Thomsen, Mikkel W. Pedersen, Hanne Jarmer, Mads Bak, Lis Hasholt, Niels Tommerup, Zeynep Tümer, Lars Allan Larsen	9
16	Screening of 99 Danish Patients with Congenital Heart Disease for GATA4 Mutations 2006 ·Genetic Testing ·Litu Zhang, Zeynep Tümer, (unknown), Paal Skytt Andersen, Niels Tommerup, Lars Allan Larsen	18
17	Hedgehog signaling in small-cell lung cancer: Frequent in vivo but a rare event in vitro 2006 ·Lung Cancer ·(unknown), Mikkel W. Pedersen, Nina Marie Pedersen, Christian Ensinger, Zeynep Tümer, Niels Tommerup, Hans Skovgaard Poulsen, Lars Allan Larsen	64
18	Identification of a Novel EYA1 Splice-Site Mutation in a Danish Branchio-Oto-Renal Syndrome Family 2004 ·Genetic Testing ·(unknown), Zeynep Tümer, Niels Tommerup, Lisbeth Tranebjærg, Lars Allan Larsen	7
19	X-Linked Menkes Disease: First Documented Report of Germ-Line Mosaicism 2004 ·Genetic Testing ·(unknown), Lisbeth Birk Møller, Katie Plunkett, John W. Belmont, Zeynep Tümer, Nina Horn	6
20	Menkes disease: recent advances and new aspects. 1997 ·Journal of Medical Genetics ·Zeynep Tümer, Nina Horn	61

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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