Amanda Collins

4.6k total citations
36 papers, 1.6k citations indexed

About

Amanda Collins is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Amanda Collins has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 14 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Amanda Collins's work include Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Chromosomal and Genetic Variations (4 papers). Amanda Collins is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Chromosomal and Genetic Variations (4 papers). Amanda Collins collaborates with scholars based in United Kingdom, United States and Netherlands. Amanda Collins's co-authors include Patrick F. Sullivan, N R Dennis, Alfredo Orrico, Anita Rauch, Christiane Zweier, Lilian Bomme Ousager, André Reis, Merel A.W. Oortveld, Annette Schenck and Emilia K. Bijlsma and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Amanda Collins

36 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amanda Collins United Kingdom 18 944 824 209 135 130 36 1.6k
Anne Moncla France 24 1.3k 1.4× 1.1k 1.3× 343 1.6× 52 0.4× 89 0.7× 38 1.9k
Jobst Meyer Germany 19 1.3k 1.4× 1.2k 1.5× 120 0.6× 79 0.6× 155 1.2× 48 2.3k
Eli Hatchwell United States 24 984 1.0× 1.2k 1.4× 534 2.6× 128 0.9× 129 1.0× 52 2.1k
Jorge Saraiva Portugal 20 866 0.9× 690 0.8× 118 0.6× 84 0.6× 81 0.6× 73 1.6k
Bronwyn Kerr United Kingdom 32 1.3k 1.4× 1.6k 1.9× 436 2.1× 49 0.4× 153 1.2× 67 3.2k
Christopher T. Gordon France 20 531 0.6× 594 0.7× 325 1.6× 133 1.0× 39 0.3× 58 1.4k
Philippe Demougin Switzerland 25 432 0.5× 1.1k 1.3× 110 0.5× 50 0.4× 107 0.8× 49 2.0k
Donatella Milani Italy 24 994 1.1× 1.3k 1.5× 183 0.9× 30 0.2× 59 0.5× 118 2.1k
C. T. R. M. Schrander‐Stumpel Netherlands 24 1.4k 1.5× 671 0.8× 209 1.0× 61 0.5× 160 1.2× 86 2.1k
Nancy J. Carpenter United States 24 1.2k 1.3× 1.0k 1.2× 325 1.6× 60 0.4× 184 1.4× 72 2.2k

Countries citing papers authored by Amanda Collins

Since Specialization
Citations

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

Fields of papers citing papers by Amanda Collins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Collins

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Collins. A scholar is included among the top collaborators of Amanda Collins 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 Amanda Collins. Amanda Collins 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.
Collins, Amanda, Joanna Maselko, Ashley Hagaman, et al.. (2024). Disability severity and risk of new or recurrent intimate partner violence – Evidence from a cohort study in rural Pakistan. Disability and health journal. 18(1). 101673–101673. 2 indexed citations
2.
Kharbanda, Mira, Mark S. Bateman, David Hunt, et al.. (2020). Directly Transmitted 12.3-Mb Deletion with a Consistent Phenotype in the Variable 11q21q22.3 Region. Cytogenetic and Genome Research. 160(4). 185–192. 1 indexed citations
3.
Bateman, Mark S., Morag N. Collinson, David J. Bunyan, et al.. (2017). Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities. American Journal of Medical Genetics Part A. 176(2). 319–329. 5 indexed citations
4.
Pengelly, Reuben J., Rosanna Upstill‐Goddard, Julio Martínez, et al.. (2014). Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole‐exome sequencing. Clinical Genetics. 88(5). 441–449. 15 indexed citations
5.
Collins, Amanda, et al.. (2014). Transcriptional targets of the schizophrenia risk gene MIR137. Translational Psychiatry. 4(7). e404–e404. 40 indexed citations
6.
Collins, Amanda, Young-Jae Kim, Pamela Sklar, Michael O’Donovan, & Patrick F. Sullivan. (2011). Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results. Psychological Medicine. 42(3). 607–616. 71 indexed citations
7.
Tan, Tiong Yang, Amanda Collins, Paul A. James, et al.. (2011). Phenotypic variability of distal 22q11.2 copy number abnormalities. American Journal of Medical Genetics Part A. 155(7). 1623–1633. 54 indexed citations
8.
Barber, John, Shuwen Huang, Mark S. Bateman, & Amanda Collins. (2011). Transmitted deletions of medial 5p and learning difficulties; Does the cadherin cluster only become penetrant when flanking genes are deleted?. American Journal of Medical Genetics Part A. 155(11). 2807–2815. 6 indexed citations
9.
Zweier, Christiane, Eiko K. de Jong, Markus Zweier, et al.. (2009). CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila. The American Journal of Human Genetics. 85(5). 655–666. 244 indexed citations
10.
Balasubramanian, Meena & Amanda Collins. (2009). Aplasia cutis congenita, terminal limb defects and periventricular leukomalacia in one sibling with minor findings in the other-probable autosomal recessive Adams-Oliver Syndrome. European Journal of Medical Genetics. 52(4). 234–238. 11 indexed citations
11.
Züchner, Stephan, Jens R. Wendland, Allison E. Ashley‐Koch, et al.. (2008). Multiple rare SAPAP3 missense variants in trichotillomania and OCD. Molecular Psychiatry. 14(1). 6–9. 132 indexed citations
12.
Collins, Amanda & Janet Holmshaw. (2008). Early detection: a survey of secondary school teachers' knowledge about psychosis. Early Intervention in Psychiatry. 2(2). 90–97. 21 indexed citations
13.
Bunyan, David J., Emma Ashton, Julie Sillibourne, et al.. (2007). Simultaneous MLPA-based multiplex point mutation and deletion analysis of the Dystrophin gene. Molecular Biotechnology. 35(2). 135–140. 22 indexed citations
14.
Barber, John, Shuai Zhang, Amanda Collins, et al.. (2006). Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenetic and Genome Research. 114(3-4). 351–358. 18 indexed citations
15.
Willatt, Lionel, James J. Cox, John Barber, et al.. (2005). 3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome. The American Journal of Human Genetics. 77(1). 154–160. 166 indexed citations
16.
Goodman, Frances R., Frank Majewski, Amanda Collins, & Peter Scambler. (2002). A 117-kb Microdeletion Removing HOXD9–HOXD13 and EVX2 Causes Synpolydactyly. The American Journal of Human Genetics. 70(2). 547–555. 77 indexed citations
17.
Collins, Amanda. (2002). Greater than Emperor. University of Michigan Press eBooks. 2 indexed citations
18.
Collins, Amanda, et al.. (1995). Crossover analysis in a British family suggests that Coffin‐Lowry syndrome maps to a 3.4‐cM interval in Xp22. American Journal of Medical Genetics. 59(4). 512–516. 12 indexed citations
19.
Collins, Amanda, N R Dennis, Neville P. Clarke, & F M Pope. (1995). A mother and three daughters with congenital dislocation of the hip and a characteristic facial appearance: a new syndrome?. Clinical Dysmorphology. 4(4). 277–282. 1 indexed citations
20.
Collins, Amanda, et al.. (1988). Skin rash associated with Candida guilliermondii. Medical and Pediatric Oncology. 16(4). 295–296. 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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