B Wittwer

883 total citations
6 papers, 514 citations indexed

About

B Wittwer is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, B Wittwer has authored 6 papers receiving a total of 514 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Oncology. Recurrent topics in B Wittwer's work include Retinal Development and Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and RNA regulation and disease (2 papers). B Wittwer is often cited by papers focused on Retinal Development and Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and RNA regulation and disease (2 papers). B Wittwer collaborates with scholars based in Germany, Italy and United Kingdom. B Wittwer's co-authors include Maria Raquel Santos Carvalho, Thomas Meitinger, Birgit Lorenz, Helene Achatz, Katherine L. Dry, Michele D’Urso, Heide Hellebrand, Eberhart Zrenner, Forbes Manson and Alan F. Wright and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

B Wittwer

6 papers receiving 506 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B Wittwer Germany	5	468	156	128	113	61	6	514
Katherine L. Dry United Kingdom	10	528 1.1×	164 1.1×	143 1.1×	117 1.0×	69 1.1×	13	592
Carmela Migliaccio Italy	5	415 0.9×	150 1.0×	126 1.0×	104 0.9×	53 0.9×	8	494
Leen Abu Safieh Saudi Arabia	11	428 0.9×	197 1.3×	144 1.1×	67 0.6×	54 0.9×	21	527
Leen Abu‐Safieh Saudi Arabia	9	544 1.2×	117 0.8×	168 1.3×	71 0.6×	59 1.0×	16	621
Brian W. Rigatti United States	10	290 0.6×	82 0.5×	127 1.0×	173 1.5×	23 0.4×	13	401
Anna M. Siemiatkowska Netherlands	14	392 0.8×	126 0.8×	216 1.7×	64 0.6×	54 0.9×	24	461
Konstantinos Nikopoulos Switzerland	12	623 1.3×	214 1.4×	143 1.1×	106 0.9×	60 1.0×	20	802
Béatrice Bocquet France	16	527 1.1×	80 0.5×	264 2.1×	90 0.8×	87 1.4×	37	607
Roberta Tammaro Italy	11	515 1.1×	180 1.2×	87 0.7×	91 0.8×	70 1.1×	12	615

Countries citing papers authored by B Wittwer

Since Specialization

Citations

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

Fields of papers citing papers by B Wittwer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Wittwer

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

All Works

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6 of 6 papers shown

1.

Herrmann, Martin, et al.. (2000). Clinical presentation and mutation identification in the NBS1 gene in a boy with Nijmegen breakage syndrome. Clinical Genetics. 57(5). 384–387. 9 indexed citations

2.

Gaudenz, Karin, Erich Roessler, Nandita Quaderi, et al.. (1998). Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain. The American Journal of Human Genetics. 63(3). 703–710. 57 indexed citations

3.

Meindl, A, Katherine L. Dry, Karin A. Herrmann, et al.. (1996). A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3). Nature Genetics. 13(1). 35–42. 391 indexed citations

4.

Wittwer, B, et al.. (1996). New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3. American Journal of Medical Genetics. 64(1). 42–49. 7 indexed citations

5.

Meindl, Alfons, Maria Raquel Santos Carvalho, Klaus M. Herrmann, et al.. (1995). A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa. Human Molecular Genetics. 4(12). 2339–2346. 49 indexed citations

6.

Wittwer, B, et al.. (1994). Gene of a new X-linked syndrome with multiple congenital anomalies and severe mental retardation maps in Xp22-pter. The American Journal of Human Genetics. 55. 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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