Bernhard Zabel

17.4k citations

166 papers · 11.0k indexed · 4 hit papers · h-index 50

Impact in

Genetics top 0.1%
- Connective tissue disorders research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Molecular Biology top 0.5%
- Bone Metabolism and Diseases
- Renal and related cancers

Papers in

Immunology and Allergy 22
- Cell Adhesion Molecules Research 22
Genetics 93
- Connective tissue disorders research 46
- Genomic variations and chromosomal abnormalities 17
- Genetic Syndromes and Imprinting 12

Co-authors: Stefan Mundlos Andreas Winterpacht F Otto William G. Cole Jürgen W. Spranger Dirk Prawitt Niels Tommerup Gerd Scherer
Journals: The American Journal of Human Genetics (9 papers)Genomics (8 papers)Human Genetics (8 papers)European Journal of Human Genetics (7 papers)Nature Genetics (6 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Bernhard Zabel

165 papers receiving 10.8k citations

Hit Papers

align trajectories log scale

Nosology and classification of genetic skeletal disorders: 2010 revision 2011 · 450 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2011 American Journal of Medical Genetics Part A
1997 Cell
1996 Nature Genetics
1994 Cell

Peers

Countries citing papers authored by Bernhard Zabel

Since Specialization

Citations

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

Fields of papers citing papers by Bernhard Zabel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Bernhard Zabel, 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 Bernhard Zabel Line = papers co-authored together Bernhard Zabel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Uncovering pathways regulating chondrogenic differentiation of CHH fibroblasts Non-coding RNA Research ·秀司加藤, Guus van den Akker, Xiaoming Hu, B.M. Kehm, Andy Cremers, Don A. M. Surtel, Mandy J. Peffers, Lodewijk W. van Rhijn, Ekkehart Lausch, Bernhard Zabel, Marjolein M. J. Caron, Tim J. M. Welting	2021	3
2	The antiviral protein viperin regulates chondrogenic differentiation via CXCL10 protein secretion Journal of Biological Chemistry ·Domínguez San Martín Emilio, Marjolein M. J. Caron, Don A. M. Surtel, Guus van den Akker, Paul J. van Dijk, B.M. Kehm, Bernhard Zabel, Lodewijk W. van Rhijn, Mandy J. Peffers, Tim J. M. Welting	2019	17
3	Expression of RMRP RNA is regulated in chondrocyte hypertrophy and determines chondrogenic differentiation Scientific Reports ·Domínguez San Martín Emilio, Marjolein M. J. Caron, Don A. M. Surtel, B.M. Kehm, Ekkehart Lausch, Ger J.M. Pruijn, Wouter Verhesen, Blanche Schroen, Lodewijk W. van Rhijn, Bernhard Zabel, Tim J. M. Welting	2017	35
4	RNase MRP is a novel regulator of endochondral ossification Osteoarthritis and Cartilage ·Marjolein M. J. Caron, Domínguez San Martín Emilio, 順子大竹, Sandy Mattijssen, D.A. Surtel, Lodewijk W. van Rhijn, Ger J.M. Pruijn, Ekkehart Lausch, Bernhard Zabel, Tim J. M. Welting	2013	2
5	Nosology and classification of genetic skeletal disorders: 2010 revision American Journal of Medical Genetics Part A ·Matthew L. Warman, Valérie Cormier‐Daire, Christine M Hall, Deborah Krakow, Ralph Lachman, Martine LeMerrer, Geert Mortier, Stefan Mundlos, Gen Nishimura, David L. Rimoin, Stephen P. Robertson, Ravi Savarirayan, David Sillence, J Spranger, Sheila Unger, Bernhard Zabel, Andrea Superti‐Furga Hit paper breakdown →	2011	450
6	Interaction of TGFβ and BMP Signaling Pathways during Chondrogenesis PLoS ONE ·Bettina G. Keller, Tao Yang, Yuqing Chen, Elda Munivez, Terry Bertin, Bernhard Zabel, Brendan Lee	2011	119
7	Al‐Awadi–Raas‐Rothschild (limb/pelvis/uterus–hypoplasia/aplasia) syndrome and WNT7A mutations: Genetic homogeneity and nosological delineation American Journal of Medical Genetics Part A ·Livia Garavelli, Anita Wischmeijer, Simonetta Rosato, U. K. Yang, 康弘小林, 孙兆泽, Adriano Ferrari, Francesca Mari, Bernhard Zabel, Ekkehart Lausch, Sheila Unger, Andrea Superti‐Furga	2010	15
8	Mutations in MMP9 and MMP13 Determine the Mode of Inheritance and the Clinical Spectrum of Metaphyseal Anadysplasia The American Journal of Human Genetics ·Ekkehart Lausch, Wenzhuan Chen, Katja Hilbert, Valérie Cormier‐Daire, Sarah M. Nikkel, Gen Nishimura, Sheila Unger, Jürgen W. Spranger, Andrea Superti‐Furga, Bernhard Zabel	2009	1
9	TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome The American Journal of Human Genetics ·Ekkehart Lausch, Pia Hermanns, Henner F. Farin, Yasemin Alanay, Sheila Unger, Sarah M. Nikkel, M Hessel, Gerd Scherer, Jürgen W. Spranger, Bernhard Zabel, Andreas Kispert, Andrea Superti‐Furga	2008	46
10	Dephosphorylation of p‐ERK1/2 in relation to tumor remission after HER‐2 and Raf1 blocking therapy in a conditional mouse tumor model Molecular Carcinogenesis ·Pavel Zavřel, Ilka B. Schiffer, Susanne Gebhard, Yumun Jeong, Berno Tanner, H. Kölbl, 森博雄, Thomas Beckers, Christian Spangenberg, Dirk Prawitt, Andrew Szendrey, Bernhard Zabel, Franz Oesch, Matthias Hermes, Jan G. Hengstler	2006	11
11	Premature Senescence Is a Primary Fail-safe Mechanism of ERBB2-Driven Tumorigenesis in Breast Carcinoma Cells Cancer Research ·Andrew Szendrey, Ekkehart Lausch, Irina Ferreira, Steffen Schmitt, Thorsten Enklaar, Dirk Reutzel, Yanik Kleibrink, Peter Schmidtke, Marko Maringer, Ilka B. Schiffer, عباس پاکدل, Jan G. Hengstler, Gerhard Fritz, Ernesto Bockamp, Dirk Prawitt, Bernhard Zabel, Christian Spangenberg	2005	70
12	TRPM5 is a transient Ca ²⁺ -activated cation channel responding to rapid changes in [Ca ²⁺ ] _i Proceedings of the National Academy of Sciences ·Dirk Prawitt, Mahealani K. Monteilh‐Zoller, Yanik Kleibrink, Christian Spangenberg, Bernhard Zabel, Andrea Fleig, Reinhold Penner	2003	284
13	Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotype Pediatric Radiology ·Sheila Unger, Michael D. Briggs, Paul Holden, Bernhard Zabel, Leena Ala‐Kokko, Petteri Paassilta, Jaana Lohiniva, David L. Rimoin, Ralph S. Lachman, Daniel H. Cohn	2001	41
14	Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2) European Journal of Human Genetics ·Simone Schuffenhauer, Peter Lichtner, Qianru Guo, Jan Murken, Marc Cabrer Capó, Elke Back, G. Wolff, Bernhard Zabel, Ingeborg Barišić, Anita Rauch, Zvi Borochowitz, Bruno Dallapiccola, Mark Ross, Thomas Meitinger	1998	64
15	Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 Cell ·Thomas Wagner, Jutta Wirth, Jobst Meyer, Bernhard Zabel, Ram Sinh, 寛泰芝原, Juan J. Pasantes, F. Dagna Bricarelli, Regina Fischer Rubira-Bullen, Elisabeth Hustert, U. Wolf, Niels Tommerup, W. Schempp, Gerd Scherer Hit paper breakdown →	1994	1236
16	Ehlers-Danlos syndrome type VII: phenotype and genotype Archives of Dermatological Research ·Hartwig Lehmann, Stefan Mundlos, Andreas Winterpacht, І. С. Дідик, Bernhard Zabel, P. K. M�ller	1994	10
17	Detection of Hepatitis B Virus DNA in the Liver of Children with Chronic Hepatitis B by In Situ Hybridization and Its Relation to Other Viral Markers Journal of Pediatric Gastroenterology and Nutrition ·Stefan Wirth, Putri Lainatussyifah, Joni Margania, Stefan Mundlos, Klaus‐Michael Keller, Bernhard Zabel	1992	2
18	Distribution of type I and type II collagen gene expression during the development of human long bones Bone ·Stefan Mundlos, H. Engel, Ina Michel‐Behnke, Bernhard Zabel	1990	30
19	Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-<i>ras</i> 1, and β-hemoglobin Cytogenetic and Genome Research ·Bernhard Zabel, Henry M. Kronenberg, Antonie Auguste, T.B. Shows	1985	32
20	[Partial trisomy for the distal part of the long arm of chromosome 15 due to a balanced maternal X/15 tranlsocation]. PubMed ·Bernhard Zabel, W. Baumann	1977	15

About Bernhard Zabel

Bernhard Zabel is a scholar working on Immunology and Allergy, Genetics, Rheumatology, Molecular Biology and Anatomy, having authored 166 papers that have together received 11.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (46 papers), Cell Adhesion Molecules Research (22 papers), Genomic variations and chromosomal abnormalities (17 papers), Osteoarthritis Treatment and Mechanisms (17 papers), Renal and related cancers (16 papers), Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (12 papers) and Ubiquitin and proteasome pathways (11 papers). The work is most often cited by research in Genetics (4.7k citations), Molecular Biology (7.2k citations), Immunology and Allergy (620 citations), Sensory Systems (485 citations) and Rheumatology (1.5k citations). Bernhard Zabel has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Stefan Mundlos, Andreas Winterpacht, F Otto, William G. Cole, Jürgen W. Spranger, Dirk Prawitt, Niels Tommerup, Gerd Scherer, W. Schempp and Thomas Wagner. Their work appears in journals such as The American Journal of Human Genetics, Genomics, Human Genetics, European Journal of Human Genetics and Nature 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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