F.F. Brockschmidt

563 total citations
8 papers, 225 citations indexed

About

F.F. Brockschmidt is a scholar working on Urology, Molecular Biology and Dermatology. According to data from OpenAlex, F.F. Brockschmidt has authored 8 papers receiving a total of 225 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Urology, 4 papers in Molecular Biology and 2 papers in Dermatology. Recurrent topics in F.F. Brockschmidt's work include Hair Growth and Disorders (5 papers), RNA regulation and disease (3 papers) and Dermatology and Skin Diseases (2 papers). F.F. Brockschmidt is often cited by papers focused on Hair Growth and Disorders (5 papers), RNA regulation and disease (3 papers) and Dermatology and Skin Diseases (2 papers). F.F. Brockschmidt collaborates with scholars based in Germany, Belgium and United Kingdom. F.F. Brockschmidt's co-authors include Markus M. Nöthen, Axel M. Hillmer, Tim Becker, Kerstin U. Ludwig, Roland Kruse, Helmut Remschmidt, Gerd Schulte‐Körne, Bertram Müller‐Myhsok, Christine Herold and Nina Neuhoff and has published in prestigious journals such as Molecular Psychiatry, British Journal of Dermatology and Journal of Molecular Endocrinology.

In The Last Decade

F.F. Brockschmidt

8 papers receiving 218 citations

Peers

F.F. Brockschmidt

UROLO

MB

GENET

DEP

CB

Nadine Kluck Germany

J.‐P. Ernst Germany

Maria Antonietta Palmas Italy

Marianna Yusupova United States

Joanna Tan Singapore

Sher Alam Khan Pakistan

JC Oosterwijk Netherlands

Aline Petrin United States

Hyun Ji Noh United States

Nadine Kluck Germany

F.F. Brockschmidt

31 ×0.3

UROLO

94 ×1.3

MB

166 ×2.7

GENET

140 ×2.5

DEP

19 ×0.4

CB

Citations per year, relative to F.F. Brockschmidt F.F. Brockschmidt (= 1×) peers Nadine Kluck

Countries citing papers authored by F.F. Brockschmidt

Since Specialization

Citations

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

Fields of papers citing papers by F.F. Brockschmidt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F.F. Brockschmidt

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Zink, Alexander M., Eva Wohlleber, Hartmut Engels, et al.. (2014). Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies. Molecular Syndromology. 5(2). 65–75. 6 indexed citations

2.

Heilmann‐Heimbach, Stefanie, Dale R. Nyholt, F.F. Brockschmidt, et al.. (2013). No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia. Queensland's institutional digital repository (The University of Queensland). 2 indexed citations

3.

Heilmann‐Heimbach, Stefanie, F.F. Brockschmidt, Axel M. Hillmer, et al.. (2013). Evidence for a polygenic contribution to androgenetic alopecia. British Journal of Dermatology. 169(4). 927–930. 30 indexed citations

4.

Redler, Silke, F.F. Brockschmidt, Christine Herold, et al.. (2012). Investigation of selected cytokine genes suggests that IL2RA and the TNF / LTA locus are risk factors for severe alopecia areata. British Journal of Dermatology. 167(6). 1360–1365. 32 indexed citations

5.

Redler, Silke, F.F. Brockschmidt, Rachid Tazi‐Ahnini, et al.. (2012). Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss. British Journal of Dermatology. 166(6). 1314–1318. 36 indexed citations

6.

Roeske, Darina, Kerstin U. Ludwig, Nina Neuhoff, et al.. (2009). First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. Molecular Psychiatry. 16(1). 97–107. 77 indexed citations

7.

Redler, Silke, F.F. Brockschmidt, Kathrin Giehl, et al.. (2009). The TRAF1/C5 locus confers risk for familial and severe alopecia areata. British Journal of Dermatology. 162(4). 866–869. 16 indexed citations

8.

Brockschmidt, F.F., Markus M. Nöthen, & Axel M. Hillmer. (2007). The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function. Journal of Molecular Endocrinology. 39(1). 1–8. 26 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.

Explore authors with similar magnitude of impact