Birgit Weiß
Impact in
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- Sexual Differentiation and Disorders
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
-
- Genomics and Chromatin Dynamics 5
- Retinoids in leukemia and cellular processes 2
- Genetics 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Gudrun Rappold (22 shared papers)Stefan Kirsch (4 shared papers)Beate Niesler (2 shared papers)Maki Fukami (3 shared papers)Tsutomu Ogata (3 shared papers)Gerhard Binder (2 shared papers)Gabriele Nordsiek (1 shared paper)Koji Muroya (1 shared paper)
- Journals
- Nature Genetics (3 papers)Frontiers in Endocrinology (2 papers)Genomics (2 papers)Frontiers in Genetics (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Birgit Weiß
24 papers receiving 1.7k citations
Birgit Weiß's Hit Papers
Peers
Comparison fields: 5 of 87
- Genetics 1.1k
- Molecular Biology 935
- Cognitive Neuroscience 257
- Gender Studies 116
- Developmental Biology 24
Countries citing papers authored by Birgit Weiß
This map shows the geographic impact of Birgit Weiß'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 Birgit Weiß with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Weiß more than expected).
Fields of papers citing papers by Birgit Weiß
This network shows the impact of papers produced by Birgit Weiß. 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 Birgit Weiß. The network helps show where Birgit Weiß may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgit Weiß, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome Hit paper breakdown → | 1997 | 764 |
| 2 | 2010 | 439 | |
| 3 | 1993 | 75 | |
| 4 | 1994 | 66 | |
| 5 | 2001 | 56 | |
| 6 | 2007 | 51 | |
| 7 | 2016 | 40 | |
| 8 | 2003 | 38 | |
| 9 | 1994 | 33 | |
| 10 | 2017 | 31 | |
| 11 | 2005 | 28 | |
| 12 | 2019 | 20 | |
| 13 | 1995 | 19 | |
| 14 | 2016 | 19 | |
| 15 | 2004 | 18 | |
| 16 | 2017 | 17 | |
| 17 | The definition of the Y chromosome growth-control gene (GCY) critical region: relevance of terminal and interstitial deletions. | 2002 | 13 |
| 18 | 2020 | 12 | |
| 19 | 2018 | 11 | |
| 20 | 2021 | 5 |
About Birgit Weiß
Birgit Weiß is a scholar working on Molecular Biology, Genetics, Endocrinology, Diabetes and Metabolism, Immunology and Cellular and Molecular Neuroscience, having authored 24 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genomics and Chromatin Dynamics (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Retinoids in leukemia and cellular processes (2 papers), interferon and immune responses (2 papers), Thyroid Disorders and Treatments (2 papers) and Autism Spectrum Disorder Research (2 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (935 citations), Cognitive Neuroscience (257 citations), Gender Studies (116 citations) and Developmental Biology (24 citations). Birgit Weiß has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Gudrun Rappold, Stefan Kirsch, Beate Niesler, Maki Fukami, Tsutomu Ogata, Gerhard Binder, Gabriele Nordsiek, Koji Muroya, Michael B. Ranke and Ercole Rao. Their work appears in journals such as Nature Genetics, Frontiers in Endocrinology, Genomics, Frontiers in Genetics and Human Molecular Genetics.
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.