Antje Brockschmidt

480 total citations
6 papers, 290 citations indexed

About

Antje Brockschmidt is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Antje Brockschmidt has authored 6 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Surgery. Recurrent topics in Antje Brockschmidt's work include Congenital heart defects research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Antje Brockschmidt is often cited by papers focused on Congenital heart defects research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Antje Brockschmidt collaborates with scholars based in Germany, United Kingdom and Poland. Antje Brockschmidt's co-authors include Ruthild G. Weber, Alexander Hoischen, Hartmut Engels, Peter Lichter, Bernhard Radlwimmer, Christina Landwehr, Wolfgang Driever, Christian Kubisch, Soojin Ryu and Stefanie Birnbaum and has published in prestigious journals such as Neurology, Human Molecular Genetics and British Journal of Cancer.

In The Last Decade

Antje Brockschmidt

6 papers receiving 274 citations

Peers

Antje Brockschmidt

GENET

MB

CN

PPCH

SURGE

Frédérique Sloan‐Béna Switzerland

Chad Haldeman‐Englert United States

Erica H. Gerkes Netherlands

Elham Sadighi Akha United Kingdom

Dalit Ben‐Yosef Israel

Val Davison United Kingdom

Lee Turnpenny United Kingdom

Claudia Ciaccio Italy

Stefanie Birnbaum Germany

Eleni Katzaki Italy

Frédérique Sloan‐Béna Switzerland

Antje Brockschmidt

87 ×0.4

GENET

123 ×0.7

MB

24 ×0.7

CN

30 ×0.9

PPCH

15 ×0.6

SURGE

Citations per year, relative to Antje Brockschmidt Antje Brockschmidt (= 1×) peers Frédérique Sloan‐Béna

Countries citing papers authored by Antje Brockschmidt

Since Specialization

Citations

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

Fields of papers citing papers by Antje Brockschmidt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antje Brockschmidt

This figure shows the co-authorship network connecting the top 25 collaborators of Antje Brockschmidt. A scholar is included among the top collaborators of Antje 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 Antje Brockschmidt. Antje 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:

6 of 6 papers shown

1.

Tomczak, Aurelie, Christoph Springfeld, Michael T. Dill, et al.. (2022). Precision oncology for intrahepatic cholangiocarcinoma in clinical practice. British Journal of Cancer. 127(9). 1701–1708. 19 indexed citations

2.

Engels, Hartmut, Herdit M. Schüler, Alexander M. Zink, et al.. (2012). A phenotype map for 14q32.3 terminal deletions. American Journal of Medical Genetics Part A. 158A(4). 695–706. 24 indexed citations

3.

Brockschmidt, Antje, Alida Filippi, Peter Charbel Issa, et al.. (2011). Neurologic and ocular phenotype in Pitt–Hopkins syndrome and a zebrafish model. Human Genetics. 130(5). 645–655. 25 indexed citations

4.

Brockschmidt, Antje, Byung Ha Chung, Stefanie Weber, et al.. (2011). CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrology Dialysis Transplantation. 27(6). 2355–2364. 28 indexed citations

5.

Brockschmidt, Antje, Unda Todt, Soojin Ryu, et al.. (2007). Severe mental retardation with breathing abnormalities (Pitt–Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4. Human Molecular Genetics. 16(12). 1488–1494. 121 indexed citations

6.

Engels, Hartmut, Antje Brockschmidt, Alexander Hoischen, et al.. (2007). DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation. Neurology. 68(10). 743–750. 73 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