A. Schinzel

438 total citations
8 papers, 247 citations indexed

About

A. Schinzel is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Ophthalmology. According to data from OpenAlex, A. Schinzel has authored 8 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Ophthalmology. Recurrent topics in A. Schinzel's work include Retinal Development and Disorders (2 papers), Congenital heart defects research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). A. Schinzel is often cited by papers focused on Retinal Development and Disorders (2 papers), Congenital heart defects research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). A. Schinzel collaborates with scholars based in Switzerland, Germany and United States. A. Schinzel's co-authors include Claudio Castellan, Mariluce Riegel, Lukrecija Brečević, Damina Balmer, J Frézal, Maximilian Muenke, Lap‐Chee Tsui, Fiorella Gurrieri, D.J. Cockburn and Barbara J. Trask and has published in prestigious journals such as Nature Genetics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

A. Schinzel

8 papers receiving 245 citations

Peers

A. Schinzel

MB

GENET

PPCH

EPIDE

DB

Rowena S. James United Kingdom

Claudine Fear United Kingdom

Mahmoud Taleb Al‐Ali United Arab Emirates

F. Ammann Switzerland

Hubert Smeets Netherlands

Anna Wawrocka Poland

Marisol Mirabelli-Badenier Italy

M. Neugebauer Germany

Shams Anazi Saudi Arabia

Yukiko Kuroda Japan

Rowena S. James United Kingdom

A. Schinzel

91 ×0.5

MB

109 ×0.8

GENET

62 ×1.6

PPCH

17 ×0.8

EPIDE

7 ×0.4

DB

Citations per year, relative to A. Schinzel A. Schinzel (= 1×) peers Rowena S. James

Countries citing papers authored by A. Schinzel

Since Specialization

Citations

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

Fields of papers citing papers by A. Schinzel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Schinzel

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

All Works

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8 of 8 papers shown

1.

Reis, Linda M., Rebecca C. Tyler, Eric Weh, et al.. (2016). Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies. Clinical Genetics. 90(4). 378–382. 13 indexed citations

2.

Riegel, Mariluce, Claudio Castellan, Damina Balmer, Lukrecija Brečević, & A. Schinzel. (1999). Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromes. American Journal of Medical Genetics. 82(3). 249–253. 48 indexed citations

3.

Bonnet, Damien, Anna Pelet, Laurence Legeai‐Mallet, et al.. (1994). A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12. Nature Genetics. 6(4). 405–408. 33 indexed citations

4.

Gurrieri, Fiorella, Barbara J. Trask, Ger van den Engh, et al.. (1993). Physical mapping of the holoprosencephaly critical region on chromosome 7q36. Nature Genetics. 3(3). 247–251. 73 indexed citations

5.

Frézal, J, et al.. (1990). Report of the committee on clinical disorders and chromosomal deletion syndromes. Cytogenetic and Genome Research. 55(1-4). 321–357. 25 indexed citations

6.

Gal, Andreas, A. Schinzel, Ulrike Orth, et al.. (1989). Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp. Human Genetics. 81(4). 315–318. 35 indexed citations

7.

Boltshauser, Eugen, A. Schinzel, W. Wichmann, Dieter Haller, & Anton Valavanis. (1988). Pelizaeus-Merzbacher disease: identification of heterozygotes with magnetic resonance imaging?. Human Genetics. 80(4). 393–394. 19 indexed citations

8.

Frézal, J, et al.. (1988). Report of the committee on clinical disorders and chromosomal deletion syndromes. Cytogenetic and Genome Research. 49(1-3). 254–256. 1 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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