Andreas Gal

413 total citations
12 papers, 288 citations indexed

About

Andreas Gal is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Andreas Gal has authored 12 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Andreas Gal's work include Retinal Development and Disorders (3 papers), Photoreceptor and optogenetics research (2 papers) and Neurological diseases and metabolism (2 papers). Andreas Gal is often cited by papers focused on Retinal Development and Disorders (3 papers), Photoreceptor and optogenetics research (2 papers) and Neurological diseases and metabolism (2 papers). Andreas Gal collaborates with scholars based in Germany, Australia and Netherlands. Andreas Gal's co-authors include Dorien van de Pol, Hans‐Hilger Ropers, Alfons Meindl, Thomas Meitinger, Wolfgang Berger, Mette Warburg, Frans P.M. Cremers, Liesbeth M. Bleeker-Wagemakers, Ulrich Kellner and Sigrid Fuchs and has published in prestigious journals such as Human Molecular Genetics, Genomics and Human Mutation.

In The Last Decade

Andreas Gal

12 papers receiving 281 citations

Peers

Countries citing papers authored by Andreas Gal

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Gal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Gal

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Gittrige Hornhautdystrophie Typ I. Klinische und molekulargenetische Untersuchung in einer großen Familie 1998 ·Klinische Monatsblätter für Augenheilkunde ·Moritz Meins, (unknown), Gisbert Richard, Andreas Gal	6
2	Identification of 16 sulfamidase gene mutations including the common R74C in patients with mucopolysaccharidosis type IIIA (Sanfilippo A) 1997 ·Human Mutation ·Susanna Bunge, Hüseyin İnce, Cordula Steglich, (unknown), Michael Beck, Jacek Zaremba, Otto P. van Diggelen, Birgit Weber, (unknown), Andreas Gal	51
3	Norrie‐Warburg syndrome: Two novel mutations in patients with classical clinical phenotype 1996 ·Acta Ophthalmologica Scandinavica ·Andreas Gal, Andres Veske, (unknown), Barbara Grammatico, Bernd Huber, Sumin Gu, Giuseppe Del Porto, (unknown)	3
4	Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa 1996 ·Ophthalmic Genetics ·Marianne Haim, Kathrin Grundmann, Andreas Gal, Thomas Rosenberg	8
5	Missense mutation (Arg121Trp) in the norrie disease gene associated with X-linked exudative vitreoretinopathy 1995 ·Human Mutation ·Sigrid Fuchs, Ulrich Kellner, (unknown), Andreas Gal	27
6	Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,xxy male heterozygous for a missense point mutation 1994 ·Prenatal Diagnosis ·Susanna Bunge, Cordula Steglich, Peter Lorenz, Michael Beck, Suying Xu, John J. Hopwood, Andreas Gal	5
7	Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene 1992 ·Documenta Ophthalmologica ·(unknown), (unknown), Albert Schinzel, Andreas Gal	20
8	Mutations in the candidate gene for Norrie disease 1992 ·Human Molecular Genetics ·Wolfgang Berger, Dorien van de Pol, Mette Warburg, Andreas Gal, Liesbeth M. Bleeker-Wagemakers, (unknown), Alfons Meindl, Thomas Meitinger, Frans P.M. Cremers, Hans‐Hilger Ropers	102
9	No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian families 1991 ·Human Genetics ·(unknown), (unknown), (unknown), (unknown), J E Olsson, (unknown), Robert Buttery, Andreas Gal, M. J. Denton	7
10	Posthumous diagnosis of X-linked retinoschisis using DNA analysis 1990 ·Ophthalmic Paediatrics and Genetics ·Mary J. van Schooneveld, Elisabeth M. Bleeker‐Wagemakers, Ulrike Orth, M. Neugebauer, (unknown), Andreas Gal	1
11	Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity 1989 ·Clinical Genetics ·Andreas Gal, Brunhilde Wirth, Helena Kääriäinen, G Lucotte, Paul Landais, (unknown), Dirk E. Müller‐Wiefel, Klaus Zerres	21
12	Two different genes for X-linked retinitis pigmentosa 1988 ·Genomics ·Brunhilde Wirth, Michael J. Denton, (unknown), M. Neugebauer, (unknown), Mary van Schooneveld, Jennifer A. Donald, Elisabeth M. Bleeker‐Wagemakers, P. Pearson, Andreas Gal	37

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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