Peter M. Kroisel

3.5k citations

38 papers · 1.5k indexed · 1 hit paper · h-index 16

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 10%
- Epigenetics and DNA Methylation
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics

Papers in

Genetics 18
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 5
- Chronic Lymphocytic Leukemia Research 2
Developmental Biology 1

Co-authors: Pieter J. de Jong Chris T. Amemiya Hiroaki Shizuya Mark A. Batzer Jeffrey Garnes Klaus Wagner Erwin Petek Christian Windpassinger
Journals: American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Prenatal Diagnosis (2 papers)Nature Genetics (2 papers)Cytogenetic and Genome Research (2 papers)Molecular Genetics and Genomics (1 paper)
Partner nations: Austria United States Canada

In The Last Decade

Peter M. Kroisel

38 papers receiving 1.4k citations

Hit Papers

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A new bacteriophage P1–derived vector for the propagation of large human DNA fragments 1994 · 681 citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2 American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Peter J. Gianakopoulos, Yuzhi Zhang, Nela Pencea, M Orlic-Milacic, Kirti Mittal, Christian Windpassinger, S.W. White, Peter M. Kroisel, Eva W.C. Chow, Carol Saunders, Berge A. Minassian, John B. Vincent	2011	21
2	Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close toSH3TC2,ADRB2, andHTR4on 5q, and within the desmocollin gene cluster on 18q American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·John B. Vincent, Abdul Noor, Christian Windpassinger, Peter J. Gianakopoulos, Thomas Schwarzbraun, Simon E. Alfred, P Wilkinson, Stephen W. Scherer, Wendy Roberts, Klaus Wagner, Peter M. Kroisel, Erwin Petek	2008	11
3	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
4	Williams-Beuren syndrome associated with caudal regression syndrome and coagulopathy—a case report Journal of Pediatric Surgery ·Georg Singer, Johannes Schalamon, Herwig Ainoedhofer, Erwin Petek, Peter M. Kroisel, Michael E. Höllwarth	2005	4
5	Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene Journal of Human Genetics ·심재구, Jochen Raedle, Christian Windpassinger, Thomas Schwarzbraun, Peter M. Kroisel, Klaus Wagner, Erwin Petek	2005	10
6	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, 심재구, A. Fahmi Abdullah, Peter M. Kroisel, Klaus Wagner, Erwin Petek	2004	20
7	Fetal nucleated red blood cells in peripheral blood of pregnant women: detection and determination of location on a slide using laser‐scanning cytometry Prenatal Diagnosis ·Simone Hennerbichler, Peter M. Kroisel, A Tiguli・saimaiti, Barbara Pertl, Reinhold Wintersteiger, Gottfried Dohr, Peter Sedlmayr	2003	13
8	Detection and relocation of cord blood nucleated red blood cells by laser scanning cytometry Cytometry ·Simone Hennerbichler, Nicholas Haraus, Erwin Petek, Peter M. Kroisel, Barbara Pertl, Beate Tiran, Gottfried Dohr, Reinhold Wintersteiger, Peter Sedlmayr	2002	5
9	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
10	Molecular characterization of a 12q22‐q24 deletion associated with congenital deafness: Confirmation and refinement of the DFNA25 locus American Journal of Medical Genetics Part A ·Erwin Petek, Christian Windpassinger, Nora R. Eibergen, Yan Tszaikhuei, Stephen W. Scherer, Klaus Wagner, Peter M. Kroisel	2002	18
11	Simultaneous occurrence of retinoblastoma and neurofibromatosis I in a young child Medical and Pediatric Oncology ·Martin Köestenberger, Peter M. Kroisel, Helmut Lackner, Christian Urban	2002	3
12	Chronic myeloid leukemia with a rare variant Philadelphia translocation Cancer Genetics and Cytogenetics ·Tong Jiang, A. Behmel, Yong Asm, H. L. Seewann, Erwin Petek, Peter M. Kroisel, Klaus Wagner	2001	10
13	Maternal methylation imprints on human chromosome 15 are established during or after fertilization Nature Genetics ·Osman El‐Maarri, Karin Buiting, 雅士泉, Peter M. Kroisel, Başak Balaban, Klaus Wagner, Bülent Urman, 陽一金森, Christina Lich, Camilynn I. Brannan, Jörn Walter, Bernhard Horsthemke	2001	159
14	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
15	Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome American Journal of Medical Genetics ·Tong Jiang, Erwin Petek, Peter M. Kroisel, A Tiguli・saimaiti, Klaus Wagner	2001	12
16	Prenatal diagnosis of partial trisomy 4q26-qter and monosomy for the Wolf-Hirschhorn critical region in a fetus with split hand malformation Prenatal Diagnosis ·Erwin Petek, Klaus Wagner, H. Steiner, H. Schaffer, Peter M. Kroisel	2000	14
17	Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH Clinical Dysmorphology ·Erwin Petek, A. F. Abu-Sarra, I Mutz, 晓娟姚, Peter M. Kroisel	2000	7
18	PCR probes for chromosome in situ hybridization of large-insert bacterial recombinants Cytogenetic and Genome Research ·Peter M. Kroisel, Griselda Abril Costas, Pieter J. de Jong	1994	15
19	TXK, a novel human tyrosine kinase expressed in T cells shares sequence identity with Tec family kinases and maps to 4p12 Human Molecular Genetics ·Robert N. Haire, Yuko Ohta, Janet E. Lewis, Shu Man Fu, Peter M. Kroisel, Gary W. Litman	1994	74
20	A Taql RFLP detected by the probe TN157 (D7S145) at the human chromosome region 7p13 – 14.2 Nucleic Acids Research ·Klaus Wagner, Peter M. Kroisel, W Rosenkranz	1991	3

About Peter M. Kroisel

Peter M. Kroisel is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Genetics and Hematology, having authored 38 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Autism Spectrum Disorder Research (4 papers), Fetal and Pediatric Neurological Disorders (4 papers), RNA and protein synthesis mechanisms (3 papers), Hedgehog Signaling Pathway Studies (3 papers) and Chronic Lymphocytic Leukemia Research (2 papers). The work is most often cited by research in Genetics (658 citations), Molecular Biology (935 citations), Genetics (109 citations), Pediatrics, Perinatology and Child Health (148 citations) and Developmental Biology (14 citations). Peter M. Kroisel has collaborated with scholars based in Austria, United States and Canada. Frequent co-authors include Pieter J. de Jong, Chris T. Amemiya, Hiroaki Shizuya, Mark A. Batzer, Jeffrey Garnes, Klaus Wagner, Erwin Petek, Christian Windpassinger, M Zach and George Polgar. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Prenatal Diagnosis, Nature Genetics, Cytogenetic and Genome Research and Molecular Genetics and Genomics.

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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