Klaus Zerres

22.8k citations

337 papers · 12.0k indexed · h-index 58

Impact in

Genetics top 0.05%
- Neurogenetic and Muscular Disorders Research
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
Molecular Biology top 0.5%
- RNA modifications and cancer
- Renal and related cancers
- RNA Research and Splicing

Papers in

Genetics 77
- Genetic and Kidney Cyst Diseases 77
- Neurogenetic and Muscular Disorders Research 72
- Genetic Syndromes and Imprinting 57
Developmental Biology 9

Co-authors: Sabine Rudnik‐Schöneborn Thomas Eggermann Brunhilde Wirth Carsten Bergmann Eric Hahnen Jan Senderek Lisa M. Guay‐Woodford Jutta Schönling
Journals: Human Genetics (12 papers)Neuromuscular Disorders (12 papers)NeuroImage (9 papers)The American Journal of Human Genetics (8 papers)European Journal of Human Genetics (8 papers)
Partner nations: Germany United States Poland

In The Last Decade

Klaus Zerres

329 papers receiving 11.6k citations

Peers

Countries citing papers authored by Klaus Zerres

Since Specialization

Citations

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

Fields of papers citing papers by Klaus Zerres

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Klaus Zerres, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Klaus Zerres Line = papers co-authored together Klaus Zerres links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Pontocerebellar hypoplasia American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Sabine Rudnik‐Schöneborn, P. G. Barth, Klaus Zerres	2014	52
2	The impact of a Dysbindin schizophrenia susceptibility variant on fiber tract integrity in healthy individuals: A TBSS-based diffusion tensor imaging study NeuroImage ·Thomas Nickl‐Jockschat, Tony Stöcker, Valentin Markov, Axel Krug, Fernanda de Blas López, Frank Schneider, Ute Habel, Klaus Zerres, Markus M. Nöthen, Jens Treutlein, Marcella Rietschel, N. Jon Shah, Tilo Kircher	2011	20
3	Sequence Variations in Subjects with Self-Reported Multiple Chemical Sensitivity (sMCS): A Case-Control Study Journal of Toxicology and Environmental Health ·Gerhard A. Wiesmüller, Hiltrud Niggemann, 勇治山本, Stefán Magni Árnason, O.V. Mevsha, Wolfgang Dott, H.J. Kunert, Klaus Zerres, Thomas Eggermann, Brunhilde Blömeke	2008	25
4	RSPO4 Is the Major Gene in Autosomal-Recessive Anonychia and Mutations Cluster in the Furin-Like Cysteine-Rich Domains of the Wnt Signaling Ligand R-spondin 4 Journal of Investigative Dermatology ·Nadina Ortiz Brüchle, Jorge Frank, Valeska Frank, Jan Senderek, Ahmet Rüçhan Akar, Erol Koç, Dimitris Rigopoulos, Maurice A. M. Van Steensel, Klaus Zerres, Carsten Bergmann	2007	35
5	Detektion von Sequenzvarianten mittels DHPLC : Etablierung als automatisiertes Verfahren zur direkten Mutationsanalyse bei autosomal-rezessiver polyzystischer Nierenerkrankung RWTH Publications (RWTH Aachen) ·Christian Dornia, Klaus Zerres	2006	0
6	Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci The American Journal of Human Genetics ·Luigi Bisceglia, Giuseppina Cerullo, Paola Forabosco, Diletta Domenica Torres, Francesco Scolari, Lise Dion-Levert, Marina Foramitti, Antonio Amoroso, Sara Bertok, Jürgen Floege, Peter R. Mertens, Klaus Zerres, Efstathios Alexopoulos, Dimitrios Kirmizis, 徐晨华, Leopoldo Zelante, Francesco Paolo Schena	2006	81
7	Risk Analyses for the Cognitive Phenotype in Turner's Syndrome: Evidence of Familial Influence as a Decisive Factor Journal of Child Neurology ·Fritz Haverkamp, Klaus Zerres, Christian Rietz, Meinolf Noeker, Antônia Fernanda de Almeida Wright	2004	1
8	The interleukin-6 promoter polymorphism is associated with elevated leukocyte, lymphocyte, and monocyte counts and reduced physical fitness in young healthy smokers Journal of Molecular Medicine ·Jan R. Ortlepp, Quang Dieu Nguyen, Raquel Delgado Mederos, J. Tendil, Fabian Schmitz, Vanessa Cunha Prado D'Afonseca, MM Phillips, Peter Hanrath, Christian Weber, Klaus Zerres, R. Hoffmann	2003	39
9	Psychopathology and familial stress – comparison of boys with Fragile X syndrome and Spinal Muscular Atrophy Journal of Child Psychology and Psychiatry ·Alexander von Gontard, Steffen Pielström, Michele Andreani, Anna Frey, Gerd Lehmkuhl, Klaus Zerres, Sabine Rudnik‐Schöneborn	2002	35
10	Cystinuria in children: Distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes Kidney International ·Elke Botzenhart, Udo Vester, Christa K. Schmidt, Albrecht Hesse, صبرى عثمان محمد حسن, Carsten A. Wagner, Florian Läng, Peter F. Hoyer, Klaus Zerres, Thomas Eggermann, (unknown)	2002	2
11	Mutations in the SLC3A1 Gene in Cystinuric Patients: Frequencies and Identification of a Novel Mutation Genetic Testing ·Alexandra Albers, Sven Lahme, Carsten A. Wagner, Peter Kaiser, Klaus Zerres, Giovambattista Capasso, Xueguang Zhou, Manuel Palacı́n, Florian Läng, Karl‐Horst Bichler, Thomas Eggermann	1999	20
12	Increased risk for abnormal placentation in women affected by myotonic dystrophy Journal of Perinatal Medicine ·Sabine Rudnik‐Schöneborn, Janne Vihinen, Klaus Zerres	1998	4
13	Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2β Genes & Development ·Markus Moser, Armin Pscherer, Christina Roth, Jutta Becker, Gabi Mücher, Klaus Zerres, Christa Dixkens, Joachim Weis, Lisa M. Guay‐Woodford, Reinhard Buettner, Reinhard Fässler	1997	226
14	Missense Mutations in Exon 6 of the Survival Motor Neuron Gene in Patients with Spinal Muscular Atrophy (SMA) Human Molecular Genetics ·Eric Hahnen, Jutta Schönling, Sabine Rudnik‐Schöneborn, A Gulley, Klaus Zerres, Brunhilde Wirth	1997	89
15	Current Status of DNA Diagnosis for Hereditary Nephropathies Kidney & Blood Pressure Research ·Klaus Zerres, MA Xian-xia	1996	1
16	Autosomal recessive polycystic kidney disease Nephrology Dialysis Transplantation ·Klaus Zerres, Sabine Rudnik‐Schöneborn, C. Steinkamm, Gabi Mücher	1996	11
17	Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophy. PubMed Central ·Sabine Rudnik‐Schöneborn, Brunhilde Wirth, Klaus Zerres	1994	11
18	Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A. PubMed ·Johannes Oldenburg, R. Schwaab, T. Grimm, Klaus Zerres, 恵理子赤井, Hans‐Hermann Brackmann, K. Olek	1993	19
19	Johanson-Blizzard-Syndrom Klinische Pädiatrie ·Sabine Rudnik‐Schöneborn, B Keller, F. A. Beemer, Mario Glavac, Кушнир Роман Николаевич, Klaus Zerres	1991	3
20	Late Manifestation of Autosomal-Recessive Polycystic Kidney Disease in Two Sisters American Journal of Nephrology ·Hartmut P.H. Neumann, Klaus Zerres, Xuehui Huang, G. Wolff, Hans E. Schaefer, Andreas Gal, Brunhilde Wirth, GU Renfu, Klaus Haag, P. Schollmeyer	1988	11

About Klaus Zerres

Klaus Zerres is a scholar working on Genetics, Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 337 papers that have together received 12.0k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (77 papers), Neurogenetic and Muscular Disorders Research (72 papers), Renal and related cancers (58 papers), Genetic Syndromes and Imprinting (57 papers), RNA modifications and cancer (46 papers), Congenital Anomalies and Fetal Surgery (33 papers), Prenatal Screening and Diagnostics (28 papers) and RNA Research and Splicing (23 papers). The work is most often cited by research in Genetics (4.1k citations), Genetics (4.3k citations), Molecular Biology (7.7k citations), Pediatrics, Perinatology and Child Health (1.6k citations) and Nephrology (400 citations). Klaus Zerres has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Sabine Rudnik‐Schöneborn, Thomas Eggermann, Brunhilde Wirth, Carsten Bergmann, Eric Hahnen, Jan Senderek, Lisa M. Guay‐Woodford, Jutta Schönling, I Hausmanowa-Pétrusewicz and Luiz F. Onuchic. Their work appears in journals such as Human Genetics, Neuromuscular Disorders, NeuroImage, The American Journal of Human Genetics and European Journal of Human Genetics.

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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