Astrid Golla

1.1k total citations
25 papers, 806 citations indexed

About

Astrid Golla is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Astrid Golla has authored 25 papers receiving a total of 806 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Molecular Biology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Astrid Golla's work include Genetics and Neurodevelopmental Disorders (5 papers), Craniofacial Disorders and Treatments (4 papers) and Cystic Fibrosis Research Advances (4 papers). Astrid Golla is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Craniofacial Disorders and Treatments (4 papers) and Cystic Fibrosis Research Advances (4 papers). Astrid Golla collaborates with scholars based in Germany, United States and Austria. Astrid Golla's co-authors include Thomas Meitinger, Heide Hellebrand, Alfons Meindl, Simone Schuffenhauer, Juliane Ramser, R. Zahn, Bernd H. Belohradsky, Annette Jansson, Thomas Klockgether and Susanna Moskau and has published in prestigious journals such as Stroke, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Astrid Golla

25 papers receiving 780 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Astrid Golla Germany 15 333 317 143 117 105 25 806
N S Thomas United Kingdom 15 257 0.8× 580 1.8× 80 0.6× 48 0.4× 38 0.4× 31 768
B. Le Marec France 19 474 1.4× 506 1.6× 67 0.5× 23 0.2× 115 1.1× 67 1.0k
Lakshmi Mehta United States 16 348 1.0× 403 1.3× 59 0.4× 21 0.2× 96 0.9× 46 754
Silvia Majore Italy 16 319 1.0× 427 1.3× 63 0.4× 66 0.6× 42 0.4× 48 808
Ann Haskins Olney United States 19 716 2.2× 842 2.7× 63 0.4× 37 0.3× 169 1.6× 43 1.4k
Mark J. Stephan United States 15 263 0.8× 279 0.9× 40 0.3× 17 0.1× 230 2.2× 23 762
Yolande van Bever Netherlands 18 441 1.3× 297 0.9× 56 0.4× 12 0.1× 218 2.1× 46 871
Kouji Narahara Japan 18 500 1.5× 509 1.6× 41 0.3× 19 0.2× 50 0.5× 52 877
James V. Higgins United States 18 414 1.2× 332 1.0× 109 0.8× 11 0.1× 241 2.3× 39 927
T. Regalia Romania 12 44 0.1× 264 0.8× 33 0.2× 65 0.6× 216 2.1× 18 655

Countries citing papers authored by Astrid Golla

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Astrid Golla

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

All Works

20 of 20 papers shown
1.
Hillmer, Axel M., Antònia Flaquer, S. Hanneken, et al.. (2008). Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26. The American Journal of Human Genetics. 82(3). 737–743. 48 indexed citations
2.
Dufault, Michael R., Beate Betz, Barbara Wappenschmidt, et al.. (2004). Limited relevance of the CHEK2 gene in hereditary breast cancer. International Journal of Cancer. 110(3). 320–325. 70 indexed citations
3.
Jamra, Rami Abou, Johannes Schumacher, Astrid Golla, et al.. (2003). Family‐based association studies of α‐adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 126B(1). 79–81. 5 indexed citations
4.
Strauch, Konstantin, Astrid Golla, Marsha Wilcox, & Max P. Baur. (2003). Genetic analysis of phenotypes derived from longitudinal data: Presentation Group 1 of Genetic Analysis Workshop 13. Genetic Epidemiology. 25(S1). S5–S17. 6 indexed citations
5.
Golla, Astrid, Konstantin Strauch, Johannes Dietter, & Max P. Baur. (2003). Quantitative trait linkage analysis of longitudinal change in body weight. BMC Genetics. 4(Suppl 1). S7–S7. 8 indexed citations
6.
Golla, Astrid, et al.. (2002). MRX42: Two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation. American Journal of Medical Genetics. 107(1). 18–25. 2 indexed citations
7.
Golla, Astrid, Annette Jansson, Juliane Ramser, et al.. (2002). Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22. European Journal of Human Genetics. 10(3). 217–221. 130 indexed citations
8.
9.
Holinski‐Feder, Elke, Edwin Reyniers, Sabine Uhrig, et al.. (2000). Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3). The American Journal of Human Genetics. 66(1). 16–25. 43 indexed citations
10.
Holinski‐Feder, Elke, Olaf Rittinger, Kerry Baldwin Jedele, et al.. (1999). Nonsyndromic X-linked mental retardation: Mapping of MRX58 to the pericentromeric region. American Journal of Medical Genetics. 86(2). 102–106. 9 indexed citations
11.
Stuhrmann, Manfred, Thilo Dörk, Matthias Frühwirth, et al.. (1997). Detection of 100% of the CFTR mutations in 63 CF families from Tyrol. Clinical Genetics. 52(4). 240–246. 18 indexed citations
12.
Schindelhauer, Dirk, Michael Weiss, Heide Hellebrand, et al.. (1996). Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product. Human Genetics. 98(1). 68–76. 75 indexed citations
13.
Schuffenhauer, Simone, Astrid Golla, Peter Lichtner, et al.. (1996). Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p. American Journal of Medical Genetics. 63(1). 177–184. 14 indexed citations
14.
Holinski‐Feder, Elke, Astrid Golla, Imma Rost, et al.. (1996). Regional localization of two MRX genes to Xq28 (MRX28) and to Xp11.4-Xp22.12 (MRX33). American Journal of Medical Genetics. 64(1). 125–130. 18 indexed citations
15.
Golla, Astrid, et al.. (1995). An Evaluation of FASTMAP with Emphasis on Fine-Mapping. Human Heredity. 45(4). 199–205. 1 indexed citations
16.
17.
Meitinger, Thomas, et al.. (1993). In frame deletion (ΔF311) within a short trinucleotide repeat of the first transmembrane region of the cystic fibrosis gene. Human Molecular Genetics. 2(12). 2173–2174. 3 indexed citations
18.
19.
Deufel, Thomas, Astrid Golla, David Iles, et al.. (1992). Evidence for genetic heterogeneity of malignant hyperthermia susceptibility.. PubMed. 50(6). 1151–61. 60 indexed citations
20.
Meitinger, Thomas, Babett Heye, Christine Petit, et al.. (1990). Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232.. PubMed. 47(4). 664–9. 53 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.

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