Peter M. Kroisel

3.5k citations

55 papers · 2.8k · 1 hit paper · h-index 23

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Molecular Biology top 10%
- Epigenetics and DNA Methylation
- Congenital heart defects research

Papers in

Genetics 25
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 6
- Congenital Ear and Nasal Anomalies 3
Pediatrics, Perinatology and Child Health 8
- Prenatal Screening and Diagnostics 5

Co-authors: Hiroaki Shizuya (1 shared paper)Jeffrey A. Garnes (1 shared paper)Mark A. Batzer (1 shared paper)Chris T. Amemiya (1 shared paper)Pieter J. de Jong (2 shared papers)Klaus Wagner (21 shared papers)Erwin Petek (23 shared papers)Christian Windpassinger (14 shared papers)
Journals: Nature Genetics (4 papers)Journal of Medical Genetics (3 papers)The American Journal of Human Genetics (2 papers)Prenatal Diagnosis (2 papers)Human Mutation (2 papers)
Partner nations: Austria United States Germany

In The Last Decade

Peter M. Kroisel

54 papers receiving 2.6k citations

Peter M. Kroisel's Hit Papers

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A new bacteriophage P1–derived vector for the propagation of large human DNA fragments 1994 · 689 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

1994 Nature Genetics

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

Showing the 20 most-cited of 55 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A new bacteriophage P1–derived vector for the propagation of large human DNA fragments Nature Genetics ·P.A. loannou, Chris T. Amemiya, Jeffrey A. Garnes, Peter M. Kroisel, Hiroaki Shizuya, Chira Chen, Mark A. Batzer, Pieter J. de Jong Hit paper breakdown →	1994	689
2	Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Nature ·Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G. Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen	2011	372
3	The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies Nature Genetics ·Claire E. Redin, Harrison Brand, Ryan L. Collins, Tammy Kammin, Elyse B. Mitchell, Jennelle C. Hodge, Carrie Hanscom, Vamsee K. Pillalamarri	2016	240
4	Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy Nature Genetics ·Thomas Cullup, Ay Lin Kho, Carlo Dionisi-Vici, Birgit Brandmeier, Frances J.D. Smith, Zoë L. Urry, Michael A. Simpson, Shu Yau	2012	234
5	Maternal methylation imprints on human chromosome 15 are established during or after fertilization Nature Genetics ·Osman El‐Maarri, Karin Buiting, Edwin G. Peery, Peter M. Kroisel, Başak Balaban, Klaus Wagner, Bülent Urman, Julia Heyd	2001	169
6	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	78
7	Cold Air Challenge of Airway Hyperreactivity in Children: Practical Application and Theoretical Aspects Pediatric Research ·M Zach, George Polgar, H Kump, Peter M. Kroisel	1984	61
8	Mutations in Endothelin 1 Cause Recessive Auriculocondylar Syndrome and Dominant Isolated Question-Mark Ears The American Journal of Human Genetics ·Christopher T. Gordon, Florence Petit, Peter M. Kroisel, Linda Plovmand Jakobsen, Roseli Maria Zechi‐Ceide, Myriam Oufadem, Christine Bôle‐Feysot, Solenn Pruvost	2013	61
9	High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one‐third of probands are minors Molecular Genetics & Genomic Medicine ·Stefanie Spiegler, Juliane Najm, Jian Liu, Stephanie Gkalympoudis, W. Schröder, Guntram Borck, Knut Brockmann, Miriam Elbracht	2014	57
10	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	55
11	CLMP Is Required for Intestinal Development, and Loss-of-Function Mutations Cause Congenital Short-Bowel Syndrome Gastroenterology ·Christine S. van der Werf, Tara D. Wabbersen, Nai‐Hua Hsiao, Joana Paredes, Heather Etchevers, Peter M. Kroisel, Dick Tibboel, Candice Babarit	2011	51
12	Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome Molecular Genetics and Genomics ·Erwin Petek, Thomas Schwarzbraun, Abdul Rahman Noor, Megha Patel, Kazuhiko Nakabayashi, Sanaa Choufani, Christian Windpassinger, Mara Stamenkovic	2006	51
13	Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome The American Journal of Human Genetics ·Huijun Wang, Aytaj Humbatova, Yuanxiang Liu, Wen Tao Qin, Ming-Yang Lee, Nicole Cesarato, Fanny Kortüm, Sheetal Kumar	2020	42
14	Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome Journal of Medical Genetics ·Christopher T. Gordon, Alice Vuillot, Sandrine Marlin, Erica H. Gerkes, Alex Henderson, Adila Al‐Kindy, Muriel Holder‐Espinasse, Sarah Park	2013	42
15	Phenotype of five patients with Greig syndrome and microdeletion of 7p13 American Journal of Medical Genetics ·Peter M. Kroisel, Erwin Petek, Klaus Wagner	2001	41
16	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	40
17	Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification Journal of Investigative Dermatology ·Robert W. Gruber, Clare Rogerson, Christian Windpassinger, Blerida Banushi, Anna A. Straatman-Iwanowska, Joanna Hanley, Federico Forneris, Robert Strohal	2016	37
18	AG‐exclusion zone revisited: Lessons to learn from 91 intronic NF1 3′ splice site mutations outside the canonical AG‐dinucleotides Human Mutation ·Katharina Wimmer, Esther Schamschula, Annekatrin Wernstedt, Pia Traunfellner, Albert Amberger, Johannes Zschocke, Peter M. Kroisel, Yunjia Chen	2020	26
19	New mutations in the ATM gene and clinical data of 25 AT patients Neurogenetics ·Ilja Demuth, Véronique Dutrannoy, Wilson Marques Jr, Heidemarie Neitzel, Detlev Schindler, Petja S. Dimova, Krystyńa Chrzańowska, Veneta Bojinova	2011	26
20	No evidence for mutagenic effects of ribavirin: report of two normal pregnancies The American Journal of Gastroenterology ·Karin Hegenbarth, Ute Maurer, Peter M. Kroisel, Peter Fickert, Michael Trauner, Rudolf E Stauber	2001	25

About Peter M. Kroisel

Peter M. Kroisel is a scholar working on Genetics, Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology and Cognitive Neuroscience, having authored 55 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (5 papers), Prenatal Screening and Diagnostics (5 papers), Hedgehog Signaling Pathway Studies (5 papers), RNA and protein synthesis mechanisms (4 papers), Congenital Ear and Nasal Anomalies (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.4k citations), Genetics (161 citations), Pediatrics, Perinatology and Child Health (232 citations) and Cell Biology (162 citations). Peter M. Kroisel has collaborated with scholars based in Austria, United States and Germany. Frequent co-authors include Hiroaki Shizuya, Jeffrey A. Garnes, Mark A. Batzer, Chris T. Amemiya, Pieter J. de Jong, Klaus Wagner, Erwin Petek, Christian Windpassinger, George Polgar and M Zach. Their work appears in journals such as Nature Genetics, Journal of Medical Genetics, The American Journal of Human Genetics, Prenatal Diagnosis and Human Mutation.

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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Peter M. Kroisel

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Peter M. Kroisel

Peter M. Kroisel's Hit Papers

Peers

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Fields of papers citing papers by Peter M. Kroisel

All Works

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