Erwin Petek

2.7k citations

60 papers · 1.5k indexed · h-index 21

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Neurology top 10%

Papers in ⓘ

Genetics 28
- Genomic variations and chromosomal abnormalities 20
- Genetics and Neurodevelopmental Disorders 9
Molecular Biology 24
- Hedgehog Signaling Pathway Studies 5
- RNA regulation and disease 4

Co-authors: Christian Windpassinger (27 shared papers)Klaus Wagner (28 shared papers)Peter M. Kroisel (20 shared papers)Stephen W. Scherer (8 shared papers)Thomas Schwarzbraun (12 shared papers)Joseph Cheung (4 shared papers)Michaela Auer‐Grumbach (2 shared papers)Omar Shebl (6 shared papers)
Journals: Cytogenetic and Genome Research (4 papers)Genomics (3 papers)Clinical Genetics (3 papers)The American Journal of Human Genetics (2 papers)Gene (2 papers)
Partner nations: Austria Canada Germany

In The Last Decade

Erwin Petek

59 papers receiving 1.5k citations

Peers

Countries citing papers authored by Erwin Petek

Since Specialization

Citations

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

Fields of papers citing papers by Erwin Petek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 60 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome Nature Genetics ·Christian Windpassinger, Michaela Auer‐Grumbach, Joy Irobi, Heema Patel, Erwin Petek, Gerd Hörl, Roland Malli, Johanna A. Reed, Ines Dierick, Nathalie Verpoorten, Thomas T. Warner, Christos Proukakis, Peter Van den Bergh, Christine Verellen, Lionel Van Maldergem, Luciano Merlini, Peter De Jonghe, Vincent Timmerman, Andrew H. Crosby, Klaus Wagner	2004	279
2	Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome The American Journal of Human Genetics ·Erwin Petek, Christian Windpassinger, John B. Vincent, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer, Peter M. Kroisel, Klaus W. Wagner	2001	130
3	An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1 The American Journal of Human Genetics ·Christian Windpassinger, Benedikt Schoser, Volker Straub, Sonja Hochmeister, Abdul Noor, Birgit Lohberger, Natalie Farra, Erwin Petek, Thomas Schwarzbraun, Lisa Ofner, Wolfgang N. Löscher, Klaus Wagner, Hanns Lochmüller, John B. Vincent, Stefan Quasthoff	2008	105
4	Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families Neurogenetics ·Gerald Egger, Katharina M. Roetzer, Abdul Noor, Anath C. Lionel, Huda Mahmood, Thomas Schwarzbraun, Oliver Boright, Anna Mikhailov, Christian R. Marshall, Christian Windpassinger, Erwin Petek, Stephen W. Scherer, Wolfgang Kaschnitz, John B. Vincent	2014	90
5	Quantitative and qualitative trophectoderm grading allows for prediction of live birth and gender Journal of Assisted Reproduction and Genetics ·Thomas Ebner, Katja Tritscher, Richard Bernhard Mayer, Peter Oppelt, Hans‐Christoph Duba, Maria Maurer, Gudrun Schappacher‐Tilp, Erwin Petek, Omar Shebl	2015	58
6	The human γ-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression Gene ·Christian Windpassinger, Peter M. Kroisel, Klaus Wagner, Erwin Petek	2002	53
7	Identification of the Human Cortactin-Binding Protein-2 Gene from the Autism Candidate Region at 7q31 Genomics ·Joseph Cheung, Erwin Petek, Kazuhiko Nakabayashi, Lap-Chee Tsui, John B. Vincent, Stephen W. Scherer	2001	46
8	Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome Molecular Genetics and Genomics ·Erwin Petek, Thomas Schwarzbraun, Abdul Noor, Megha Patel, Kazuhiko Nakabayashi, Sanaa Choufani, Christian Windpassinger, M. Stamenković, Mary M. Robertson, H.N. Aschauer, Hugh Gurling, Peter M. Kroisel, Klaus Wagner, Stephen W. Scherer, John B. Vincent	2006	46
9	Oocyte competence in in vitro fertilization and intracytoplasmic sperm injection patients suffering from endometriosis and its possible association with subsequent treatment outcome: a matched case–control study Acta Obstetricia Et Gynecologica Scandinavica ·Omar Shebl, Ida Sifferlinger, Alwin Habelsberger, Peter Oppelt, Richard Bernhard Mayer, Erwin Petek, Thomas Ebner	2016	43
10	The RAY1/ST7 Tumor-Suppressor Locus on Chromosome 7q31 Represents a Complex Multi-transcript System Genomics ·John B. Vincent, Erwin Petek, Sandy Thevarkunnel, Debbie Kolozsvari, Joseph Cheung, Megha Patel, Stephen W. Scherer	2002	39
11	Candidate region for Gilles de la Tourette syndrome at 7q31 American Journal of Medical Genetics ·Peter M. Kroisel, Erwin Petek, Werner Emberger, Christian Windpassinger, Wolfgang Wladika, Klaus Wagner	2001	34
12	Is the molecular clock ticking differently in bipolar disorder? Methylation analysis of the clock gene ARNTL The World Journal of Biological Psychiatry ·Susanne Bengesser, Eva Z. Reininghaus, Nina Lackner, Armin Birner, Frederike T. Fellendorf, Martina Platzer, Nora Kainzbauer, Bernhard Tropper, Christa Hörmanseder, Robert Queissner, Hans‐Peter Kapfhammer, Sandra J. Wallner‐Liebmann, Robert Fuchs, Erwin Petek, Christian Windpassinger, Mario Schnalzenberger, Bernd Reininghaus, Bernd O. Evert, Andreas Waha	2016	32
13	Refinement of the "Silver syndrome locus" on chromosome 11q12-q14 in four families and exclusion of eight candidate genes Human Genetics ·Christian Windpassinger, Klaus Wagner, Erwin Petek, Renate Fischer, Michaela Auer‐Grumbach	2003	31
14	Localization<footref rid="foot01"><sup>1</sup></footref> of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescencein situ hybridisation Cytogenetic and Genome Research ·Erwin Petek, Christian Windpassinger, H. Egger, PM Kroisel, Kay‐Uwe Wagner	2000	26
15	Mosaicism in a fragile X male including a de novo deletion in theFMR1 gene American Journal of Medical Genetics ·Erwin Petek, Peter M. Kroisel, Margit Schuster, H Zierler, Klaus Wagner	1999	25
16	Phenotype of five patients with Greig syndrome and microdeletion of 7p13 American Journal of Medical Genetics ·Peter M. Kroisel, Erwin Petek, Klaus Wagner	2001	22
17	Time-lapse imaging provides further evidence that planar arrangement of blastomeres is highly abnormal Archives of Gynecology and Obstetrics ·Thomas Ebner, Alexandra Höggerl, Peter Oppelt, Elisabeth Radler, Simon‐Hermann Enzelsberger, Richard Bernhard Mayer, Erwin Petek, Omar Shebl	2017	21
18	Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the myelin transcription factor 1 gene (MYT1) Clinical Genetics ·T Kroepfl, Erwin Petek, Thomas Schwarzbraun, PM Kroisel, Barbara Plecko	2008	21
19	Three different profiles: Early socio-communicative capacities in typical Rett syndrome, the preserved speech variant and normal development Developmental Neurorehabilitation ·Peter B. Marschik, Katrin D. Bartl-Pokorny, Helen Tager‐Flusberg, Walter E. Kaufmann, Florian B. Pokorny, Tobias Großmann, Christian Windpassinger, Erwin Petek, Christa Einspieler	2013	21
20	Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue Genomics ·Thomas Schwarzbraun, John B. Vincent, Axel Schumacher, Daniel H. Geschwind, João Ricardo Mendes de Oliveira, Christian Windpassinger, Lisa Ofner, Michael K. Ledinegg, Peter M. Kroisel, Klaus Wagner, Erwin Petek	2004	20

About Erwin Petek

Erwin Petek is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Cell Biology, having authored 60 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (12 papers), Autism Spectrum Disorder Research (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Chromosomal and Genetic Variations (6 papers), Hedgehog Signaling Pathway Studies (5 papers), Reproductive Biology and Fertility (5 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Genetics (469 citations), Neurology (111 citations), Cellular and Molecular Neuroscience (242 citations), Genetics (132 citations) and Reproductive Medicine (104 citations). Erwin Petek has collaborated with scholars based in Austria, Canada and Germany. Frequent co-authors include Christian Windpassinger, Klaus Wagner, Peter M. Kroisel, Stephen W. Scherer, Thomas Schwarzbraun, Joseph Cheung, Michaela Auer‐Grumbach, Omar Shebl, Thomas Ebner and John B. Vincent. Their work appears in journals such as Cytogenetic and Genome Research, Genomics, Clinical Genetics, The American Journal of Human Genetics and Gene.

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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