Erwin Petek

2.7k total citations
60 papers, 1.5k citations indexed

About

Erwin Petek is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Erwin Petek has authored 60 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 24 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Erwin Petek's work include Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (12 papers) and Autism Spectrum Disorder Research (9 papers). Erwin Petek is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Prenatal Screening and Diagnostics (12 papers) and Autism Spectrum Disorder Research (9 papers). Erwin Petek collaborates with scholars based in Austria, Canada and Germany. Erwin Petek's co-authors include Christian Windpassinger, Klaus Wagner, Peter M. Kroisel, Stephen W. Scherer, Thomas Schwarzbraun, Joseph Cheung, Omar Shebl, Michaela Auer‐Grumbach, Thomas Ebner and John B. Vincent and has published in prestigious journals such as Nature Genetics, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Erwin Petek

59 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Erwin Petek Austria 21 669 469 242 229 187 60 1.5k
Kimberly A. Aldinger United States 25 1.3k 1.9× 613 1.3× 344 1.4× 365 1.6× 104 0.6× 48 2.3k
Myriam Srour Canada 20 703 1.1× 653 1.4× 320 1.3× 197 0.9× 118 0.6× 88 1.9k
Meral Topçu Türkiye 24 1.4k 2.1× 718 1.5× 399 1.6× 195 0.9× 306 1.6× 85 2.5k
Martin Begemann Germany 23 1.2k 1.7× 339 0.7× 168 0.7× 140 0.6× 147 0.8× 54 2.3k
Bert van der Zwaag Netherlands 23 1.2k 1.8× 704 1.5× 372 1.5× 200 0.9× 316 1.7× 44 2.2k
Amanda Mitchell United States 23 1.3k 2.0× 591 1.3× 248 1.0× 341 1.5× 46 0.2× 59 2.3k
Jeff M. Milunsky United States 22 704 1.1× 822 1.8× 145 0.6× 252 1.1× 122 0.7× 70 1.7k
Sabrina Buoni Italy 20 611 0.9× 745 1.6× 165 0.7× 312 1.4× 60 0.3× 56 1.4k
Vinodh Narayanan United States 25 1.2k 1.7× 749 1.6× 418 1.7× 398 1.7× 158 0.8× 67 2.3k
Carlos Cardoso France 24 1.2k 1.8× 871 1.9× 302 1.2× 211 0.9× 286 1.5× 37 2.0k

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-authorship network of co-authors of Erwin Petek

This figure shows the co-authorship network connecting the top 25 collaborators of Erwin Petek. A scholar is included among the top collaborators of Erwin Petek 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 Erwin Petek. Erwin Petek is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ahmed, Rizwan Raheem, Christian Windpassinger, Muhammad Salim, et al.. (2019). Genetic Study of Khyber-Pukhtunkhwa Resident Pakistani Families Presenting Primary Microcephaly With Intellectual Disability. Journal of the Pakistan Medical Association. 69(0). 1–1. 5 indexed citations
2.
3.
Bengesser, Susanne, Eva Z. Reininghaus, Nina Lackner, et al.. (2016). Is the molecular clock ticking differently in bipolar disorder? Methylation analysis of the clock gene ARNTL. The World Journal of Biological Psychiatry. 19(sup2). S21–S29. 32 indexed citations
4.
Ebner, Thomas, Richard Bernhard Mayer, Peter Oppelt, et al.. (2015). Quantitative and qualitative trophectoderm grading allows for prediction of live birth and gender. Journal of Assisted Reproduction and Genetics. 33(1). 49–57. 58 indexed citations
5.
Ebner, Thomas, Omar Shebl, Peter Oppelt, et al.. (2014). Viability of cumulus cells is associated with basal AMH levels in assisted reproduction. European Journal of Obstetrics & Gynecology and Reproductive Biology. 183. 59–63. 5 indexed citations
6.
Zung, Amnon, et al.. (2011). MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome. American Journal of Medical Genetics Part A. 155(10). 2469–2472. 15 indexed citations
7.
Kroneis, Thomas, Michaele Hartmann, Petra Hartmann, et al.. (2009). Automatic retrieval of single microchimeric cells and verification of identity by on‐chip multiplex PCR. Journal of Cellular and Molecular Medicine. 14(4). 954–969. 18 indexed citations
8.
Schwarzbraun, Thomas, Reinhard Ullmann, Christian Windpassinger, et al.. (2006). Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development. Cytogenetic and Genome Research. 115(1). 84–89. 6 indexed citations
9.
Varon, Raymonda, Klaus Wagner, Erwin Petek, et al.. (2006). Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8. American Journal of Medical Genetics Part A. 143A(1). 92–94. 7 indexed citations
10.
Petek, Erwin, Thomas Schwarzbraun, Abdul Noor, et al.. (2006). Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome. Molecular Genetics and Genomics. 277(1). 71–81. 46 indexed citations
11.
Singer, Georg, Johannes Schalamon, Herwig Ainoedhofer, et al.. (2005). Williams-Beuren syndrome associated with caudal regression syndrome and coagulopathy—a case report. Journal of Pediatric Surgery. 40(11). e47–e50. 4 indexed citations
12.
Schwarzbraun, Thomas, John B. Vincent, Axel Schumacher, et al.. (2004). Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue. Genomics. 84(3). 577–586. 20 indexed citations
13.
Hennerbichler, Simone, Erwin Petek, Peter M. Kroisel, et al.. (2002). Detection and relocation of cord blood nucleated red blood cells by laser scanning cytometry. Cytometry. 48(2). 87–92. 5 indexed citations
14.
Windpassinger, Christian, Peter M. Kroisel, Klaus Wagner, & Erwin Petek. (2002). The human γ-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression. Gene. 292(1-2). 25–31. 53 indexed citations
15.
Behmel, A., et al.. (2001). Chronic myeloid leukemia with a rare variant Philadelphia translocation. Cancer Genetics and Cytogenetics. 129(1). 76–79. 10 indexed citations
16.
Cheung, Joseph, Erwin Petek, Kazuhiko Nakabayashi, et al.. (2001). Identification of the Human Cortactin-Binding Protein-2 Gene from the Autism Candidate Region at 7q31. Genomics. 78(1-2). 7–11. 46 indexed citations
17.
Petek, Erwin, Christian Windpassinger, Joseph Cheung, et al.. (2001). Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome. The American Journal of Human Genetics. 68(4). 848–858. 130 indexed citations
18.
19.
Petek, Erwin, et al.. (2000). Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH. Clinical Dysmorphology. 9(1). 55–57. 7 indexed citations
20.
Petek, Erwin & Klaus Wagner. (1999). A rapid and efficient PCR approach for the generation of direct-labeled DNA probes for FISH analysis. 4(1). 45–47. 1 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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