Jacqueline Ramsay

1.1k total citations
6 papers, 316 citations indexed

About

Jacqueline Ramsay is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jacqueline Ramsay has authored 6 papers receiving a total of 316 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jacqueline Ramsay's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (2 papers) and Prenatal Screening and Diagnostics (2 papers). Jacqueline Ramsay is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (2 papers) and Prenatal Screening and Diagnostics (2 papers). Jacqueline Ramsay collaborates with scholars based in United Kingdom, Netherlands and Switzerland. Jacqueline Ramsay's co-authors include David Fitzpatrick, Dian Donnai, R. Frank Kooy, Arie P.T. Smits, Birgitta Winnepenninckx, Dominique Smeets, Dorothy Trump, Howard Martin, Kate Walker and Charles Shaw‐Smith and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Medical Genetics Part A and European Journal of Medical Genetics.

In The Last Decade

Jacqueline Ramsay

6 papers receiving 313 citations

Peers

Countries citing papers authored by Jacqueline Ramsay

Since Specialization

Citations

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

Fields of papers citing papers by Jacqueline Ramsay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Ramsay

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Sonic hedgehog mutations are an uncommon cause of developmental eye anomalies 2010 ·American Journal of Medical Genetics Part A ·Preeti Bakrania, Sı̇bel Aylı̇n Uğur İşerı̇, Alexander W. Wyatt, (unknown), Wayne Lam, Alison Salt, Jacqueline Ramsay, David Robinson, Nicola Ragge	21
2	FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality 2008 ·The American Journal of Human Genetics ·Judith A. Fantes, (unknown), Jacqueline Ramsay, Dian Donnai, Miranda Splitt, Judith A. Goodship, Helen Stewart, Margo Whiteford, Philippe Gautier, Louise Harewood, Susan M. Holloway, Freddie H. Sharkey, E.R. Maher, Veronica van Heyningen, Jill Clayton‐Smith, David Fitzpatrick, Graeme C. Black	31
3	CGG-Repeat Expansion in the DIP2B Gene Is Associated with the Fragile Site FRA12A on Chromosome 12q13.1 2007 ·The American Journal of Human Genetics ·Birgitta Winnepenninckx, (unknown), Jacqueline Ramsay, Dominique Smeets, Arie P.T. Smits, David Fitzpatrick, R. Frank Kooy	72
4	Using BAC clones to characterize unbalanced chromosome abnormalities in interphase cells 2005 ·European Journal of Medical Genetics ·(unknown), E.R. Maher, Judith A. Fantes, Jacqueline Ramsay, Roxani Angelopoulou	2
5	3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome 2005 ·The American Journal of Human Genetics ·Lionel Willatt, James J. Cox, John Barber, Elisabet Dachs Cabanas, Amanda Collins, Dian Donnai, David Fitzpatrick, (unknown), Howard Martin, (unknown), (unknown), Jacqueline Ramsay, Charles Shaw‐Smith, Erik A. Sistermans, (unknown), Dorothy Trump, Bert B.A. de Vries, Kate Walker, F. Lucy Raymond	166
6	Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3 2004 ·American Journal of Medical Genetics Part A ·Sixto García‐Miñaúr, Jacqueline Ramsay, Elizabeth Grace, Robert A. Minns, Lynn Myles, David Fitzpatrick	24

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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