Birgit Weiß

2.2k citations
22 papers · 1.8k · 1 hit paper · h-index 14

Impact in

  • Genetics top 2%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Connective tissue disorders research
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • Genomics and Rare Diseases 5
    • Connective tissue disorders research 4
    • Genomic variations and chromosomal abnormalities 2
    • Growth Hormone and Insulin-like Growth Factors 3
    • Thyroid Disorders and Treatments 2

Birgit Weiß

22 papers receiving 1.7k citations

Birgit Weiß's Hit Papers

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome 1997 · 771 citations
7710+9+19Years since publication250500750

Peers

Birgit Weiß
Comparison fields: 5 of 77
  • Genetics 1k
  • Developmental Biology 36
  • Endocrinology, Diabetes and Metabolism 274
  • Reproductive Medicine 116
  • Cognitive Neuroscience 221
Replace Ralph Roeth with:
Ralph Roeth Germany
Nobuhiro Harada Japan
Junzo Kato Japan
Adolfo D. Garnica United States
Susanne M. Cabrera United States
Antje Wiesener Germany
Mieczyslaw Michalkiewicz United States
Jaya Ganesh United States
Akie Yanai Japan
Maryvonne Warembourg France
Birgit Weiß relative to Ralph Roeth Germany Ralph Roeth's profile →
Citations per field
00.5×5×10×14.5×
Ralph Roeth · 1×
Citations per year

Countries citing papers authored by Birgit Weiß

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Birgit Weiß Line = papers co-authored together Birgit Weiß links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 22 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 →
1997771
2 2010459
3 199986
4 199373
5 200158
6 200753
7 201644
8 199433
9 201732
10 201924
11 201621
12 201720
13 199519
14 200418
15
The definition of the Y chromosome growth-control gene (GCY) critical region: relevance of terminal and interstitial deletions.
200213
16 202013
17 201811
18 20215
19 19943
20 20213

About Birgit Weiß

Birgit Weiß is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Reproductive Medicine, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 22 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 (6 papers), Genomics and Rare Diseases (5 papers), Connective tissue disorders research (4 papers), Growth Hormone and Insulin-like Growth Factors (3 papers), Thyroid Disorders and Treatments (2 papers), Schizophrenia research and treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Ion channel regulation and function (2 papers). The work is most often cited by research in Genetics (1k citations), Developmental Biology (36 citations), Endocrinology, Diabetes and Metabolism (274 citations), Reproductive Medicine (116 citations) and Cognitive Neuroscience (221 citations). Birgit Weiß has collaborated with scholars based in Germany, Netherlands and Japan. Frequent co-authors include Gudrun Rappold, Stefan Kirsch, Beate Niesler, Annelyse Mertz, Tsutomu Ogata, Maki Fukami, Gerhard Binder, Ercole Rao, M. Winkelmann and Michael B. Ranke. Their work appears in journals such as Nature Genetics, Genomics, Frontiers in Endocrinology, Genes and Journal of Medical 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.

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