Peter Miny

3.1k total citations
88 papers, 1.5k citations indexed

About

Peter Miny is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Peter Miny has authored 88 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Pediatrics, Perinatology and Child Health, 46 papers in Genetics and 17 papers in Molecular Biology. Recurrent topics in Peter Miny's work include Prenatal Screening and Diagnostics (54 papers), Genomic variations and chromosomal abnormalities (29 papers) and Fetal and Pediatric Neurological Disorders (14 papers). Peter Miny is often cited by papers focused on Prenatal Screening and Diagnostics (54 papers), Genomic variations and chromosomal abnormalities (29 papers) and Fetal and Pediatric Neurological Disorders (14 papers). Peter Miny collaborates with scholars based in Germany, Switzerland and United States. Peter Miny's co-authors include Wolfgang Holzgreve, Isabel Filges, Sevgi Tercanli, Dorothee Gänshirt-Ahlert, Karl Heinimann, Jürgen Horst, Henk Garritsen, Benno Röthlisberger, J. Horst and Friedel Wenzel and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and PEDIATRICS.

In The Last Decade

Peter Miny

85 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter Miny Germany	21	844	629	437	203	187	88	1.5k
Erik Iwarsson Sweden	21	614 0.7×	516 0.8×	507 1.2×	150 0.7×	65 0.3×	49	1.4k
Svetlana Rechitsky United States	28	1.4k 1.7×	669 1.1×	637 1.5×	387 1.9×	318 1.7×	100	2.1k
Isabel Lorda‐Sánchez Spain	23	689 0.8×	759 1.2×	558 1.3×	130 0.6×	164 0.9×	67	1.4k
Arabella Smith Australia	22	591 0.7×	1.2k 1.8×	605 1.4×	182 0.9×	31 0.2×	119	1.8k
Sioban SenGupta United Kingdom	23	1.1k 1.3×	471 0.7×	494 1.1×	203 1.0×	113 0.6×	49	1.8k
Marta Rodríguez de Alba Spain	19	566 0.7×	316 0.5×	285 0.7×	64 0.3×	231 1.2×	42	889
Nicolette S. den Hollander Netherlands	21	409 0.5×	499 0.8×	510 1.2×	183 0.9×	66 0.4×	43	1.6k
Hutton M. Kearney United States	21	1.0k 1.2×	2.2k 3.4×	1.1k 2.6×	175 0.9×	91 0.5×	40	3.2k
Suzanna G.M. Frints Netherlands	21	416 0.5×	1.1k 1.7×	878 2.0×	95 0.5×	77 0.4×	39	1.9k
Philippos C. Patsalis Cyprus	27	705 0.8×	1.2k 1.9×	1.0k 2.4×	79 0.4×	114 0.6×	100	2.0k

Countries citing papers authored by Peter Miny

Since Specialization

Citations

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

Fields of papers citing papers by Peter Miny

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Miny

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

All Works

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20 of 20 papers shown

Filges, Isabel, Peter Miny, Wolfgang Holzgreve, & Sevgi Tercanli. (2021). How genomics is changing the practice of prenatal testing. Journal of Perinatal Medicine. 49(8). 1003–1010. 5 indexed citations

Zhang, Hong, et al.. (2014). Gene Expression Profiles of Similarly Derived Human Embryonic Stem Cell Lines Correlate with Their Distinct Propensity to Exit Stemness and Their Different Differentiation Behavior in Culture. Cellular Reprogramming. 16(3). 185–195. 2 indexed citations

Hoeller, Sylvia, Michel Bihl, Alexandar Tzankov, et al.. (2014). Morphologic and GATA1 sequencing analysis of hematopoiesis in fetuses with trisomy 21. Human Pathology. 45(5). 1003–1009. 5 indexed citations

Dettmer, Matthias S., Peter Itin, Peter Miny, et al.. (2011). Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome?. Diagnostic Pathology. 6(1). 75–75. 10 indexed citations

Filges, Isabel, Anjeung Kang, Friedel Wenzel, et al.. (2011). aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis. Prenatal Diagnosis. 31(5). 473–478. 26 indexed citations

Filges, Isabel, Benno Röthlisberger, Philippe Demougin, et al.. (2010). Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clinical Genetics. 79(1). 79–85. 36 indexed citations

Vogler, Christian, Leo Gschwind, Benno Röthlisberger, et al.. (2010). Microarray-Based Maps of Copy-Number Variant Regions in European and Sub-Saharan Populations. PLoS ONE. 5(12). e15246–e15246. 19 indexed citations

Langlois, Sylvie, Paul J. Yong, Siu Li Yong, et al.. (2006). Postnatal follow‐up of prenatally diagnosed trisomy 16 mosaicism. Prenatal Diagnosis. 26(6). 548–558. 53 indexed citations

Bärtsch, Christine, Peter Miny, Jürgen Horst, et al.. (2001). Duplication Dup(1)(q32q44) Detected by Comparative Genomic Hybridization (CGH): Further Delineation of Trisomies 1q. Fetal Diagnosis and Therapy. 16(5). 265–273. 24 indexed citations

10.

Held, K. R., B. Eiben, & Peter Miny. (2000). The long-term effect of external quality assessment on performance in service cytogenetics. Cytogenetic and Genome Research. 91(1-4). 124–127. 3 indexed citations

11.

Kececioglu, Deniz, et al.. (1997). Eine seltene Kombination einer partiellen Trisomie 9 mit einer Pulmonalatresie. Klinische Pädiatrie. 209(3). 127–129. 2 indexed citations

12.

Fuhrmann, Walter, Klaus Altland, Vesna Jovanović, et al.. (1993). First‐trimester alpha‐fetoprotein screening for Down syndrome. Prenatal Diagnosis. 13(3). 215–218. 13 indexed citations

13.

Holzgreve, Wolfgang, et al.. (1993). Prenatal diagnosis and management of fetal hydrocephaly and lissencephaly. Child s Nervous System. 9(7). 408–412. 23 indexed citations

14.

Holzgreve, Wolfgang, et al.. (1993). Immediate and Long- Term Applications of Technology. Clinical Obstetrics & Gynecology. 36(3). 476–484. 5 indexed citations

15.

Gänshirt-Ahlert, Dorothee, et al.. (1990). Ratio of fetal to maternal DNA is less than 1 in 5000 at different gestational ages in maternal blood. Clinical Genetics. 38(1). 38–43. 26 indexed citations

16.

Holzgreve, Wolfgang, et al.. (1990). ‘Late CVS’ international registry compilation of data from 24 centres. Prenatal Diagnosis. 10(3). 159–167. 13 indexed citations

17.

Fuhrmann, Walter, Klaus Altland, Wolfgang Holzgreve, et al.. (1988). Feto-maternal transfusion after chorionic villus sampling. Human Genetics. 78(1). 83–85. 17 indexed citations

18.

Holzgreve, Wolfgang, et al.. (1987). Erfahrungen mit der pränatalen Diagnostik von Sichelzellenanämie und Thalassämien im ersten Schwangerschaftstrimenon: Aspekte für den Frauenarzt. Geburtshilfe und Frauenheilkunde. 47(8). 533–536. 1 indexed citations

19.

Holzgreve, Wolfgang & Peter Miny. (1987). Chorionic villi sampling with an echogenic catheter: experiences of the first 500 cases. Journal of Perinatal Medicine. 15(3). 244–250. 7 indexed citations

20.

Holzgreve, Wolfgang, Peter Miny, Ralph J. Anderson, & M S Golbus. (1987). Experience with 8 Cases of Prenatally Diagnosed Sacrococcygeal Teratomas. Fetal Diagnosis and Therapy. 2(2). 88–94. 16 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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