Peter M. Kroisel

942 total citations
18 papers, 500 citations indexed

About

Peter M. Kroisel is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Peter M. Kroisel has authored 18 papers receiving a total of 500 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Peter M. Kroisel's work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (5 papers). Peter M. Kroisel is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (5 papers). Peter M. Kroisel collaborates with scholars based in Austria, Germany and United Kingdom. Peter M. Kroisel's co-authors include Barbara Pertl, Susanne Kopp, Jon Sherlock, Lucia Tului, B. Brambati, Klaus Wagner, Matteo Adinolfí, W Rosenkranz, Klaus W. Wagner and Erwin Petek and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Obstetrics and Gynecology and Genomics.

In The Last Decade

Peter M. Kroisel

18 papers receiving 481 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter M. Kroisel Austria 14 381 248 231 59 33 18 500
Drew Duckett United Kingdom 9 249 0.7× 128 0.5× 142 0.6× 63 1.1× 12 0.4× 23 353
Catherine Metaxotou Greece 12 188 0.5× 140 0.6× 130 0.6× 66 1.1× 21 0.6× 35 334
Vikram Jaswaney United States 7 424 1.1× 154 0.6× 245 1.1× 51 0.9× 8 0.2× 12 489
Friedel Wenzel Switzerland 11 164 0.4× 145 0.6× 136 0.6× 24 0.4× 29 0.9× 21 341
Cindy Aknin France 9 293 0.8× 137 0.6× 426 1.8× 34 0.6× 19 0.6× 13 578
A Rinaldi Italy 12 191 0.5× 128 0.5× 215 0.9× 47 0.8× 10 0.3× 35 476
Chiara Palka Italy 10 210 0.6× 136 0.5× 255 1.1× 36 0.6× 24 0.7× 34 468
J. Britt Ravnan United States 12 811 2.1× 494 2.0× 408 1.8× 160 2.7× 39 1.2× 19 1.1k
Morag N. Collinson United Kingdom 14 381 1.0× 123 0.5× 210 0.9× 97 1.6× 4 0.1× 21 473
Fatimah Rahman United Kingdom 7 209 0.5× 132 0.5× 278 1.2× 19 0.3× 10 0.3× 9 439

Countries citing papers authored by Peter M. Kroisel

Since Specialization
Citations

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

Fields of papers citing papers by Peter M. Kroisel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter M. Kroisel. 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 Peter M. Kroisel. The network helps show where Peter M. Kroisel may publish in the future.

Co-authorship network of co-authors of Peter M. Kroisel

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

All Works

18 of 18 papers shown
1.
Meyer, Robert, Matthias Begemann, Alma Kuechler, et al.. (2021). One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver–Russell syndrome. Orphanet Journal of Rare Diseases. 16(1). 42–42. 17 indexed citations
2.
Hurst, Jane A., Pradeep Vasudevan, Maria Kirchhoff, et al.. (2011). Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3. European Journal of Human Genetics. 19(7). 757–762. 21 indexed citations
3.
Jakubiczka, Sibylle, Cornelis H. Schröder, Reinhard Ullmann, et al.. (2010). Translocation and Deletion around <i>SOX9</i> in a Patient with Acampomelic Campomelic Dysplasia and Sex Reversal. Sexual Development. 4(3). 143–149. 18 indexed citations
4.
Mignon‐Ravix, Cécile, D. Depétris, Judith Luciani, et al.. (2007). Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations. European Journal of Human Genetics. 15(4). 432–440. 38 indexed citations
5.
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
6.
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
7.
Kroisel, Peter M., et al.. (2005). Genetische Risikofaktoren für schizophrene Erkrankungen. PubMed. 73. 44–50. 1 indexed citations
8.
Varon, Raymonda, Denise Horn, Monika Cohen, et al.. (2004). SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. Human Genetics. 114(6). 553–561. 41 indexed citations
9.
Petek, Erwin, Christian Windpassinger, Burkhard Simma, et al.. (2003). Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies. Journal of Human Genetics. 48(6). 283–287. 18 indexed citations
10.
Holinski‐Feder, Elke, Edwin Reyniers, Sabine Uhrig, et al.. (2000). Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3). The American Journal of Human Genetics. 66(1). 16–25. 43 indexed citations
11.
Buiting, Karin, Peter M. Kroisel, Klaus Wagner, et al.. (2000). Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling. Clinical Genetics. 58(4). 284–290. 20 indexed citations
12.
Petek, Erwin, et al.. (1999). Mosaicism in a fragile X male including a de novo deletion in theFMR1 gene. American Journal of Medical Genetics. 84(3). 229–232. 25 indexed citations
13.
Pertl, Barbara, et al.. (1999). Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samples. Journal of Medical Genetics. 36(4). 300–303. 82 indexed citations
14.
Pertl, Barbara, et al.. (1997). Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sex. American Journal of Obstetrics and Gynecology. 177(4). 899–906. 51 indexed citations
15.
Pertl, Barbara, et al.. (1996). Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCR. Human Genetics. 98(1). 55–59. 67 indexed citations
16.
Wagner, Klaus W., Peter M. Kroisel, & W Rosenkranz. (1992). Localization of genes and anonymous DNA probes on the short arm of Chromosome 7. Mammalian Genome. 3(1). 39–41. 4 indexed citations
17.
Vortkamp, Andrea, Manfred Gessler, W Rosenkranz, et al.. (1991). A somatic cell hybrid panel and DNA probes for physical mapping of human chromosome 7p. Genomics. 11(3). 737–743. 16 indexed citations
18.
Wagner, Klaus W., Peter M. Kroisel, & W Rosenkranz. (1990). Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: Hemizygosity for PGAM2 and TCRG genes. Genomics. 8(3). 487–491. 25 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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