Eberhard Passarge

7.0k total citations
158 papers, 4.1k citations indexed

About

Eberhard Passarge is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eberhard Passarge has authored 158 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Genetics, 66 papers in Molecular Biology and 27 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eberhard Passarge's work include Genomic variations and chromosomal abnormalities (21 papers), DNA Repair Mechanisms (18 papers) and Prenatal Screening and Diagnostics (18 papers). Eberhard Passarge is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), DNA Repair Mechanisms (18 papers) and Prenatal Screening and Diagnostics (18 papers). Eberhard Passarge collaborates with scholars based in Germany, United States and United Kingdom. Eberhard Passarge's co-authors include Bernhard Horsthemke, James German, Valerie Greger, Elmar P. Messmer, Dietmar Lohmann, A. James McAdams, David C. Bloom, W. Lenz, Claus R. Bartram and W Höpping and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Eberhard Passarge

147 papers receiving 3.8k citations

Peers

Countries citing papers authored by Eberhard Passarge

Since Specialization

Citations

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

Fields of papers citing papers by Eberhard Passarge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eberhard Passarge

This figure shows the co-authorship network connecting the top 25 collaborators of Eberhard Passarge. A scholar is included among the top collaborators of Eberhard Passarge 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 Eberhard Passarge. Eberhard Passarge 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

#	Work	Indexed citations
1	The early years of the ESHG leading to the reform of 1988 and the spirit of the Sestri Levante school 2017 ·European Journal of Human Genetics ·G. Cara Romeo, Eberhard Passarge, Albert de la Chapelle	1
2	Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perception 2008 ·European Journal of Medical Genetics ·Martin Poot, Ruben van’t Slot, (unknown), Vera Beyer, Eberhard Passarge, Thomas Haaf	13
3	Genetische Grundlagen des Morbus Hirschsprung 2007 ·Der Pathologe ·Eberhard Passarge, Elisabeth Bruder	5
4	Prenatally detected trisomy 4 and 6 mosaicism—cytogenetic results and clinical phenotype 2003 ·Prenatal Diagnosis ·Dagmar Wieczorek, (unknown), Wendy P. Robinson, Eberhard Passarge, Gabriele Gillessen‐Kaesbach	23
5	Molekulare Genetik und Diagnostik des Retinoblastoms : Bedeutung für die Ophthalmologische Praxis 1997 ·Der Ophthalmologe ·(unknown), Burkhard Brandt, Eberhard Passarge, Bernhard Horsthemke	1
6	Molekulare Genetik und Diagnostik des Retinoblastoms 1997 ·Der Ophthalmologe ·(unknown), Burkhard Brandt, Eberhard Passarge, Bernhard Horsthemke	3
7	Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma 1994 ·Human Genetics ·(unknown), (unknown), (unknown), Eberhard Passarge, Bernhard Horsthemke	100
8	Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma 1994 ·Human Genetics ·Valerie Greger, (unknown), Dietmar Lohmann, (unknown), Eberhard Passarge, Bernhard Horsthemke	131
9	Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families 1993 ·Human Genetics ·Peter Steinbach, (unknown), Gholamali Tariverdian, Ingo Kennerknecht, Gotthold Barbi, (unknown), H. Enders, (unknown), H. Heilbronner, (unknown), Renate Kircheisen, F. Majewski, Peter Meinecke, Eberhard Passarge, A. Schmidt, Heide Seidel, G. Wolff, (unknown)	12
10	Somatic mosaicism in a patient with bilateral retinoblastoma. 1990 ·PubMed ·Valerie Greger, Eberhard Passarge, Bernhard Horsthemke	29
11	Use of the RB1 cDNA as a diagnostic probe in retinoblastoma families 1990 ·Clinical Genetics ·Audrey D. Goddard, Robert Phillips, Valerie Greger, Eberhard Passarge, W Höpping, Xiaoping Zhu, Brenda L. Gallie, Bernhard Horsthemke	15
12	No difference in expression of chromosomal fragile sites in patients with solid malignant tumours and normal controls 1990 ·Genes Chromosomes and Cancer ·(unknown), Angela Schmidt, Hugo W. Rüdiger, (unknown), Eberhard Passarge	7
13	Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma 1989 ·Human Genetics ·Valerie Greger, Eberhard Passarge, (unknown), Elmar P. Messmer, Bernhard Horsthemke	387
14	HLA‐A,B,C,DR typing and 17‐OHP determination for second trimester prenatal diagnosis of 21‐hydroxylase deficient CAH 1988 ·Prenatal Diagnosis ·H. Grosse‐Wilde, Elizabeth Valentine‐Thon, (unknown), Eberhard Passarge, F Lorenzen, Wolfgang G. Sippell, F. Bidlingmaier, Dietrich Knorr	8
15	Fragile site xq 27 clinical and cyto genetic manifestation in hemi zygotes and hetero zygotes 1981 ·Clinical Genetics ·A. Schmidt, Eberhard Passarge	1
16	Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts. 1980 ·Europe PMC (PubMed Central) ·Hugo W. Rüdiger, Claus R. Bartram, Wilhelm Harder, Eberhard Passarge	26
17	Cerebro-hepato-renal syndrome 1967 ·The Journal of Pediatrics ·Eberhard Passarge, A. James McAdams	97
18	Malformations of the central nervous system in trisomy 18 syndrome 1966 ·The Journal of Pediatrics ·Eberhard Passarge, (unknown), (unknown), (unknown), (unknown)	42
19	Epidermolysis bullosa hereditaria simplex 1965 ·The Journal of Pediatrics ·Eberhard Passarge	6
20	Endocardial Fibroelastosis 1964 ·BMJ ·Eberhard Passarge	1

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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