H. Reinwein

1.1k citations
54 papers · 782 indexed · h-index 13
Topics
Genomic variations and chromosomal abnormalities (24 papers)Chromosomal and Genetic Variations (11 papers)Prenatal Screening and Diagnostics (6 papers)
Partner nations
GermanyNorwayDenmark

In The Last Decade

H. Reinwein

49 papers receiving 708 citations

Peers

H. Reinwein
Comparison fields: 5 of 66
  • Genetics 640
  • Molecular Biology 377
  • Plant Science 216
  • Pediatrics, Perinatology and Child Health 174
  • Developmental Biology 85
Replace R. A. Pfeiffer with:
R. A. Pfeiffer Germany
R. A. Pfeiffer Germany
Elke Back Germany
Frederick W. Luthardt United States
Ernest Lieber United States
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H. Reinwein relative to R. A. Pfeiffer Germany R. A. Pfeiffer's profile →
Citations per field
00.5×
R. A. Pfeiffer · 1×
Citations per year

Countries citing papers authored by H. Reinwein

Since Specialization
Citations

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

Fields of papers citing papers by H. Reinwein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Reinwein

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

All Works

20 of 20 papers shown
#WorkIndexed citations
1 143
2
[Chlamydia pneumonia in early infancy (author's transl)].
0
3 15
4
[Congenital goitre--diagnosis, therapy and prognosis (author's transl)].
2
5 2
6 31
7 17
8 10
9
Radiological examinations of patients with autosomal aberrations.
3
10
[Report of 3 mosaic cases with G-1 trisomy (mongolism)].
2
11 8
12 16
13 11
14 2
15
[Recognition and evaluation of massive upper gastrointestinal hemorrhage].
0
16
[Clinical aspects of gout, the so-called forgotten disease].
1
17
[Concordant occurrence of liver cirrhosis and diabetes mellitus (hemochromatosis) in twins].
2
18
[Clinical aspects of porphyria cutanea tarda (hematoporphyria chronica Günther)].
3
19
[The post-cholecystectomy syndrome].
1
20
[Diabetes mellitus and ariboflavinosis].
2

About H. Reinwein

H. Reinwein is a scholar working on Developmental Biology, Genetics and Clinical Biochemistry, having authored 54 papers that have together received 782 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Chromosomal and Genetic Variations (11 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Developmental Biology (85 citations), Genetics (640 citations) and Pediatrics, Perinatology and Child Health (174 citations). H. Reinwein has collaborated with scholars based in Germany, Norway and Denmark. Frequent co-authors include U. Wolf, Helmut Baitsch, Wolfgang Engel, Walther Vogel, Holger Hoehn, Ola Didrik Saugstad, Roland Toder, Ola H. Skjeldal, Carll Goodpasture and Per Guldberg. Their work appears in journals such as The Lancet, Nature Genetics and Human Genetics.

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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