Astrid Golla
Impact in
- Genetics top 5%
- Craniofacial Disorders and Treatments
- BRCA gene mutations in cancer
- Cleft Lip and Palate Research
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Rheumatology top 5%
- Osteomyelitis and Bone Disorders Research
Papers in
- Genetics 14
- Genetics and Neurodevelopmental Disorders 5
- Craniofacial Disorders and Treatments 4
- Cleft Lip and Palate Research 3
- Genetic Mapping and Diversity in Plants and Animals 3
- Genetic Associations and Epidemiology 3
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- RNA modifications and cancer 3
- dental development and anomalies 2
- Co-authors
- Thomas Meitinger (9 shared papers)Heide Hellebrand (2 shared papers)Alfons Meindl (2 shared papers)Simone Schuffenhauer (4 shared papers)Annette Jansson (1 shared paper)R. Zahn (1 shared paper)Juliane Ramser (1 shared paper)Bernd H. Belohradsky (1 shared paper)
- Journals
- Human Molecular Genetics (2 papers)Human Mutation (2 papers)Clinical Genetics (2 papers)Genetic Epidemiology (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- GermanyAustriaUnited States
In The Last Decade
Astrid Golla
25 papers receiving 784 citations
Peers
Comparison fields: 5 of 74
- Genetics 312
- Rheumatology 139
- Urology 46
- Immunology and Allergy 40
- Reproductive Medicine 38
Countries citing papers authored by Astrid Golla
This map shows the geographic impact of Astrid Golla'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 Astrid Golla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Astrid Golla more than expected).
Fields of papers citing papers by Astrid Golla
This network shows the impact of papers produced by Astrid Golla. 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 Astrid Golla. The network helps show where Astrid Golla may publish in the future.
Co-authors
The 25 scholars most cited alongside Astrid Golla, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 130 | |
| 2 | 2004 | 90 | |
| 3 | 1996 | 75 | |
| 4 | 2004 | 70 | |
| 5 | 2000 | 61 | |
| 6 | Evidence for genetic heterogeneity of malignant hyperthermia susceptibility. | 1992 | 60 |
| 7 | Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232. | 1990 | 53 |
| 8 | 2008 | 48 | |
| 9 | 2000 | 43 | |
| 10 | 1997 | 33 | |
| 11 | 1993 | 31 | |
| 12 | 1997 | 18 | |
| 13 | 1996 | 18 | |
| 14 | 2001 | 17 | |
| 15 | 1996 | 14 | |
| 16 | 1999 | 9 | |
| 17 | 2003 | 8 | |
| 18 | 1994 | 6 | |
| 19 | 2003 | 6 | |
| 20 | 2003 | 5 |
About Astrid Golla
Astrid Golla is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cardiology and Cardiovascular Medicine and Rheumatology, having authored 25 papers that have together received 807 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Craniofacial Disorders and Treatments (4 papers), Cystic Fibrosis Research Advances (4 papers), Cleft Lip and Palate Research (3 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers), Genetic Associations and Epidemiology (3 papers), RNA modifications and cancer (3 papers) and dental development and anomalies (2 papers). The work is most often cited by research in Genetics (312 citations), Rheumatology (139 citations), Urology (46 citations), Immunology and Allergy (40 citations) and Reproductive Medicine (38 citations). Astrid Golla has collaborated with scholars based in Germany, Austria and United States. Frequent co-authors include Thomas Meitinger, Heide Hellebrand, Alfons Meindl, Simone Schuffenhauer, Annette Jansson, R. Zahn, Juliane Ramser, Bernd H. Belohradsky, Thomas Klockgether and Dirk Schindelhauer. Their work appears in journals such as Human Molecular Genetics, Human Mutation, Clinical Genetics, Genetic Epidemiology and The American Journal of Human 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.