Elisabeth Rosser

7.0k total citations
35 papers, 1.1k citations indexed

About

Elisabeth Rosser is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Elisabeth Rosser has authored 35 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 18 papers in Genetics and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Elisabeth Rosser's work include Genomics and Rare Diseases (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Elisabeth Rosser is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetic Neurodegenerative Diseases (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Elisabeth Rosser collaborates with scholars based in United Kingdom, Netherlands and United States. Elisabeth Rosser's co-authors include David Craufurd, Gail Norbury, Jayne Leggo, David C. Rubinsztein, Mathias Chiano, Neil V. Morgan, Jane A. Hurst, Jenny E.V. Morton, Lesley MacPherson and Christian J. Hendriksz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neurology.

In The Last Decade

Elisabeth Rosser

34 papers receiving 1.1k citations

Peers

Countries citing papers authored by Elisabeth Rosser

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth Rosser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Rosser

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Contribution of retrotransposition to developmental disorders 2019 ·Nature Communications ·Eugene J. Gardner, Elena Prigmore, Giuseppe Gallone, Petr Danecek, Kaitlin E. Samocha, (unknown), Sebastian S. Gerety, Holly Ironfield, Patrick Short, Alejandro Sifrim, Tarjinder Singh, Kate Chandler, Emma Clement, Katherine Lachlan, Katrina Prescott, Elisabeth Rosser, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles	39
2	Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders 2017 ·European Journal of Human Genetics ·(unknown), Alistair T. Pagnamenta, Yoshiko Murakami, John Taylor, Consuelo Anzilotti, Malcolm F. Howard, (unknown), Diana Johnson, (unknown), Sahar Mansour, I. Karen Temple, (unknown), Elisabeth Rosser, Rachel Harrison, (unknown), Niko Popitsch, Taroh Kinoshita, Jenny C. Taylor, Usha Kini	48
3	22 Years of predictive testing for Huntington’s disease: the experience of the UK Huntington’s Prediction Consortium 2016 ·European Journal of Human Genetics ·Sheharyar Baig, Mark Strong, Elisabeth Rosser, Nicola V. Taverner, (unknown), Zosia Miedzybrodzka, Angus Clarke, David Craufurd, Oliver Quarrell	57
4	Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1 2015 ·European Journal of Human Genetics ·Lemuel Racacho, (unknown), H. Robson MacDonald, Helen J. Dranse, Sarah M. Nikkel, Judith Allanson, Elisabeth Rosser, T. Michael Underhill, Dennis E. Bulman	18
5	The use of whole-exome sequencing to disentangle complex phenotypes 2015 ·European Journal of Human Genetics ·(unknown), Hywel Williams, John R. Hurst, Louise Ocaka, Chela James, C. Pao, Estelle Chanudet, Francesco Lescai, Horia Stanescu, Robert Kleta, Elisabeth Rosser, Chiara Bacchelli, Philip L. Beales	11
6	Mutations in CDK 5 RAP 2 cause Seckel syndrome 2015 ·Molecular Genetics & Genomic Medicine ·Gökhan Yigit, Karen E. Brown, Hülya Kayserili, Esther Pohl, Almuth Caliebe, (unknown), Elisabeth Rosser, Nina Bögershausen, Zehra Oya Uyguner, Umut Altunoğlu, Gudrun Nürnberg, Peter Nürnberg, Anita Rauch, Yun Li, Christian T. Thiel, Bernd Wollnik	44
7	K06 Uptake of Predictive Tests for Huntington's Disease (HD) in the UK 1993-2012 2014 ·Journal of Neurology Neurosurgery & Psychiatry ·Oliver Quarrell, Elisabeth Rosser, Nicola V. Taverner, Zosia Miedzybrodzka, Angus Clarke, David Craufurd, Mark Strong	1
8	Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature 2014 ·European Journal of Human Genetics ·Merel Klaassens, Deborah Morrogh, Elisabeth Rosser, Fatima Jaffer, Maaike Vreeburg, Levinus A. Bok, (unknown), (unknown), Rosaline C. M. Quinlivan, Ajith Kumar, Jane A. Hurst, Richard H. Scott	48
9	Developmental delay and connective tissue disorder in four patients sharing a common microdeletion at 6q13-14 2010 ·Journal of Medical Genetics ·Hilde Van Esch, Elisabeth Rosser, Sandra Janssens, (unknown), Bart Loeys, Björn Menten	16
10	Cutaneous Features Associated with Microcephalic Osteodysplastic Primordial Dwarfism Type II 2008 ·Pediatric Dermatology ·(unknown), Edel A. O’Toole, David G. Paige, Elisabeth Rosser	5
11	A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes 2008 ·Human Molecular Genetics ·Tuula Rinne, (unknown), Evert N. Lamme, Pascal H. G. Duijf, Emine Bolat, Rowdy Meijer, Hans Scheffer, Elisabeth Rosser, Tiong Yang Tan, John A. McGrath, Joost Schalkwijk, H.G. Brunner, Huiqing Zhou, Hans van Bokhoven	46
12	Mutation in Rab3 GTPase-Activating Protein (RAB3GAP) Noncatalytic Subunit in a Kindred with Martsolf Syndrome 2006 ·The American Journal of Human Genetics ·Irene A. Aligianis, Neil V. Morgan, Marina Mione, Colin A. Johnson, Elisabeth Rosser, Raoul C. M. Hennekam, Gill Adams, Richard C. Trembath, Daniela T. Pilz, Neil Stoodley, Anthony T. Moore, Steve Wilson, Eamonn R. Maher	78
13	Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination 2006 ·Neurogenetics ·Nicole I. Wolf, Maria Cundall, Paul Rutland, Elisabeth Rosser, Robert Surtees, Sarah Benton, W.K. Chong, Sue Malcolm, Friedrich Ebinger, Maria Bitner‐Glindzicz, Karen Woodward	33
14	Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation 2005 ·European Journal of Human Genetics ·David A. Koolen, William Reardon, Elisabeth Rosser, Didier Lacombe, Jane A. Hurst, (unknown), Ernie M.H.F. Bongers, Conny M.A. van Ravenswaaij‐Arts, M.A.R. Leisink, Ad Geurts van Kessel, Joris A. Veltman, Bert B.A. de Vries	38
15	Inherited cancer in children: practical/ethical problems and challenges 2004 ·European Journal of Cancer ·Marc Tischkowitz, Elisabeth Rosser	20
16	Medulloblastoma as a First Presentation of Fanconi Anemia 2003 ·Journal of Pediatric Hematology/Oncology ·Marc Tischkowitz, Julia Chisholm, Mark N. Gaze, Antony Michalski, Elisabeth Rosser	12
17	Lethal acrofacial dysostosis, pre- and post-axial defects of the hands, and bilateral renal agenesis 2002 ·Clinical Dysmorphology ·A.W. Bates, C. Michael Hall, H. R. Morgan, Elisabeth Rosser, Irene Scheimberg	6
18	Three patients with the osteochondrodysplasia and hypertrichosis syndrome - Cantu syndrome 1998 ·Clinical Dysmorphology ·Elisabeth Rosser, H Kääriäinen, Jane A. Hurst, M Baraitser, C. Michael Hall, Peter T. Clayton, James V. Leonard	25
19	Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease 1997 ·Proceedings of the National Academy of Sciences ·David C. Rubinsztein, Jayne Leggo, Mathias Chiano, (unknown), Gail Norbury, Elisabeth Rosser, David Craufurd	181
20	Serpentine fibula syndrome: expansion of the phenotype with three affected siblings 1996 ·Clinical Dysmorphology ·Elisabeth Rosser, Nick Mann, C. Michael Hall, R M Winter	15

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.

Explore authors with similar magnitude of impact