Astrid Weber

4.8k total citations
23 papers, 533 citations indexed

About

Astrid Weber is a scholar working on Genetics, Molecular Biology and Occupational Therapy. According to data from OpenAlex, Astrid Weber has authored 23 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Occupational Therapy. Recurrent topics in Astrid Weber's work include Erythropoietin and Anemia Treatment (3 papers), Craniofacial Disorders and Treatments (3 papers) and Cleft Lip and Palate Research (3 papers). Astrid Weber is often cited by papers focused on Erythropoietin and Anemia Treatment (3 papers), Craniofacial Disorders and Treatments (3 papers) and Cleft Lip and Palate Research (3 papers). Astrid Weber collaborates with scholars based in United Kingdom, United States and Germany. Astrid Weber's co-authors include Eric Corbett, Michael Obladen, Rolf F. Maier, Yu Zhong, Jeffrey P. Bigham, David B. Ascher, Mariam Jafri, N. Wake, Mark Dzietko and Eleanor Rattenberry and has published in prestigious journals such as Neurology, Brain Research and Human Molecular Genetics.

In The Last Decade

Astrid Weber

22 papers receiving 512 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Astrid Weber United Kingdom	11	201	109	84	67	64	23	533
Yiya Yang China	15	437 2.2×	84 0.8×	58 0.7×	13 0.2×	5 0.1×	39	731
David Franklin United States	16	84 0.4×	15 0.1×	58 0.7×	27 0.4×	24 0.4×	59	869
Michael Champion United Kingdom	12	199 1.0×	47 0.4×	17 0.2×	9 0.1×	17 0.3×	32	651
Shirong Wang United States	15	506 2.5×	33 0.3×	23 0.3×	218 3.3×	168 2.6×	45	1.1k
Kimberly Clark United States	16	273 1.4×	50 0.5×	15 0.2×	21 0.3×	8 0.1×	32	788
Alessandra Rufa Italy	19	424 2.1×	82 0.8×	4 0.0×	28 0.4×	12 0.2×	92	1.3k
Somnath Banerjee United Kingdom	16	126 0.6×	27 0.2×	30 0.4×	9 0.1×	9 0.1×	59	811
Kate Revill United States	16	504 2.5×	71 0.7×	12 0.1×	7 0.1×	11 0.2×	31	1.1k
Roxana Merino-Martinez Sweden	11	245 1.2×	108 1.0×	31 0.4×	25 0.4×	11 0.2×	21	587

Countries citing papers authored by Astrid Weber

Since Specialization

Citations

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

Fields of papers citing papers by Astrid Weber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Weber

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

All Works

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20 of 20 papers shown

McCann, Emma, Astrid Weber, Jenny E.V. Morton, et al.. (2024). Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis. Journal of Anatomy. 245(6). 874–878. 2 indexed citations

Calpena, Eduardo, et al.. (2023). Review of Recurrently Mutated Genes in Craniosynostosis Supports Expansion of Diagnostic Gene Panels. Genes. 14(3). 615–615. 3 indexed citations

Munteanu, Cosmin, Jenny Waycott, Robin Brewer, et al.. (2022). Alexa, Tell Me a Joke!: "Voice Interfaces are Truly Inclusive". CHI Conference on Human Factors in Computing Systems Extended Abstracts. 1–3. 4 indexed citations

Richardson, Ruth, et al.. (2018). SET de novo frameshift variants associated with developmental delay and intellectual disabilities. European Journal of Human Genetics. 26(9). 1306–1311. 6 indexed citations

Brewer, Robin, Leah Findlater, Joseph Kaye, et al.. (2018). Accessible Voice Interfaces. 441–446. 21 indexed citations

Balasubramanian, Meena, Josh Willoughby, Andrew E. Fry, et al.. (2017). Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature. Journal of Medical Genetics. 54(8). 537–543. 44 indexed citations

Kim, Sharon, Stephen R.F. Twigg, Aditi Chandra, et al.. (2017). Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans. Human Molecular Genetics. 26(11). 2118–2132. 18 indexed citations

Corbett, Eric & Astrid Weber. (2016). What can I say?. 72–82. 102 indexed citations

Benjamin, Caroline, et al.. (2015). A prospective cohort study assessing clinical referral management & workforce allocation within a UK regional medical genetics service. European Journal of Human Genetics. 23(8). 996–1003. 6 indexed citations

10.

Jedraszak, Guillaume, Bénédicte Demeer, Michèle Mathieu‐Dramard, et al.. (2015). Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients. American Journal of Medical Genetics Part A. 167(3). 504–511. 17 indexed citations

11.

Jafri, Mariam, N. Wake, David B. Ascher, et al.. (2015). Germline Mutations in theCDKN2BTumor Suppressor Gene Predispose to Renal Cell Carcinoma. Cancer Discovery. 5(7). 723–729. 77 indexed citations

12.

Giri, Dinesh, et al.. (2015). Multiple endocrine neoplasia syndromes 1 and 2: manifestations and management in childhood and adolescence. Archives of Disease in Childhood. 100(10). 994–999. 4 indexed citations

13.

Zhong, Yu, et al.. (2015). Enhancing Android accessibility for users with hand tremor by reducing fine pointing and steady tapping. 1–10. 33 indexed citations

14.

Donne, Adam J., et al.. (2014). Raine syndrome: a review and a report of metabolic bone disease as a new link. 1. 11 indexed citations

15.

Pinkney, Jonathan, et al.. (2010). Improvement in the care of multiple endocrine neoplasia Type 1 through a regional multidisciplinary clinic. QJM. 103(5). 337–345. 4 indexed citations

16.

Weber, Astrid, Mark Dzietko, Monika Berns, et al.. (2005). Neuronal damage after moderate hypoxia and erythropoietin. Neurobiology of Disease. 20(2). 594–600. 44 indexed citations

17.

Davies, Nigel P., Paola Imbrici, Doreen Fialho, et al.. (2005). Andersen–Tawil syndrome. Neurology. 65(7). 1083–1089. 79 indexed citations

18.

Hennermann, Julia B., A Loui, Astrid Weber, & E. Mönch. (2004). Hyperphenylalaninemia in a premature infant with heterozygosity for phenylketonuria. Journal of Perinatal Medicine. 32(4). 383–5. 6 indexed citations

19.

Weber, Astrid, Rolf F. Maier, Ulrike Hoffmann, et al.. (2002). Erythropoietin improves synaptic transmission during and following ischemia in rat hippocampal slice cultures. Brain Research. 958(2). 305–311. 46 indexed citations

20.

Weber, Astrid, et al.. (2001). Breast milk from mothers of very low birthweight infants: variability in fat and protein content. Acta Paediatrica. 90(7). 772–775. 4 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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