Sally Ann Lynch

14.3k total citations
146 papers, 3.7k citations indexed

About

Sally Ann Lynch is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sally Ann Lynch has authored 146 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Genetics, 59 papers in Molecular Biology and 21 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sally Ann Lynch's work include Genomics and Rare Diseases (30 papers), Genomic variations and chromosomal abnormalities (26 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Sally Ann Lynch is often cited by papers focused on Genomics and Rare Diseases (30 papers), Genomic variations and chromosomal abnormalities (26 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Sally Ann Lynch collaborates with scholars based in Ireland, United Kingdom and United States. Sally Ann Lynch's co-authors include Sean Ennis, John Burn, Judith Conroy, David Fitzpatrick, Mary D. King, Jillian P. Casey, Veronica van Heyningen, Kathy Williamson, Judy Fantes and Patricia N. Howard‐Peebles and has published in prestigious journals such as Science, Circulation and Nature Genetics.

In The Last Decade

Sally Ann Lynch

136 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sally Ann Lynch Ireland 34 1.6k 1.4k 744 379 282 146 3.7k
Peter D. Turnpenny United Kingdom 35 1.7k 1.1× 1.4k 1.0× 892 1.2× 486 1.3× 271 1.0× 109 4.0k
Arthur S. Aylsworth United States 32 1.8k 1.1× 1.9k 1.3× 575 0.8× 596 1.6× 191 0.7× 93 3.8k
Kenjiro Kosaki Japan 35 2.7k 1.7× 1.8k 1.3× 623 0.8× 591 1.6× 464 1.6× 363 5.2k
Bronwyn Kerr United Kingdom 32 1.6k 1.0× 1.3k 0.9× 480 0.6× 399 1.1× 170 0.6× 67 3.2k
Hülya Kayserili Türkiye 35 2.8k 1.7× 1.7k 1.2× 331 0.4× 473 1.2× 285 1.0× 152 4.4k
Stephen P. Robertson New Zealand 38 2.8k 1.8× 2.2k 1.6× 547 0.7× 496 1.3× 329 1.2× 152 5.3k
Domenico Coviello Italy 32 1.2k 0.7× 795 0.6× 550 0.7× 418 1.1× 207 0.7× 175 3.4k
Alan Fryer United Kingdom 33 1.5k 0.9× 1.4k 1.0× 338 0.5× 581 1.5× 194 0.7× 103 4.5k
Marwan Shinawi United States 32 2.4k 1.5× 1.5k 1.1× 336 0.5× 375 1.0× 165 0.6× 137 4.3k
Marco Seri Italy 38 2.3k 1.4× 1.4k 1.0× 1.1k 1.4× 202 0.5× 318 1.1× 193 5.3k

Countries citing papers authored by Sally Ann Lynch

Since Specialization
Citations

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

Fields of papers citing papers by Sally Ann Lynch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sally Ann Lynch. 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 Sally Ann Lynch. The network helps show where Sally Ann Lynch may publish in the future.

Co-authorship network of co-authors of Sally Ann Lynch

This figure shows the co-authorship network connecting the top 25 collaborators of Sally Ann Lynch. A scholar is included among the top collaborators of Sally Ann Lynch 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 Sally Ann Lynch. Sally Ann Lynch 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.
Lambert, Deborah M., Helen Stewart, Marta Bertoli, et al.. (2025). What is risk in clinical genetics? Designing and piloting tools to evaluate risk in clinical genetics using failure modes and effects analysis. European Journal of Human Genetics.
2.
Ochoa, Eguzkine, Magdalena Badura‐Stronka, Deirdre Donnelly, et al.. (2023). Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. European Journal of Human Genetics. 31(9). 1040–1047. 5 indexed citations
3.
Douzgou, Sofia, Hui Liang, Kay Metcalfe, et al.. (2019). The clinical presentation caused by truncating CHD8 variants. Clinical Genetics. 96(1). 72–84. 26 indexed citations
4.
Ree, Rasmus, Pernille Mathiesen Tørring, Kristina P. Sørensen, et al.. (2019). A novel NAA10 p.(R83H) variant with impaired acetyltransferase activity identified in two boys with ID and microcephaly. BMC Medical Genetics. 20(1). 101–101. 18 indexed citations
5.
Forman, Eva, et al.. (2019). X-linked infantile spinal muscular atrophy (SMAX2) caused by novel c.1681G>A substitution in the UBA1 gene, expanding the phenotype. Neuromuscular Disorders. 30(1). 35–37. 5 indexed citations
6.
7.
Casey, Jillian P., Chihiro Hisatsune, Bryan Lynch, et al.. (2017). A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca2+ signal patterns. Journal of Neurology. 264(7). 1444–1453. 23 indexed citations
8.
Lynch, Sally Ann & Isabella Borg. (2015). Wide disparity of clinical genetics services and EU rare disease research funding across Europe. Journal of Community Genetics. 7(2). 119–126. 19 indexed citations
9.
Casey, Jillian P., Svein I. Støve, Catherine McGorrian, et al.. (2015). NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment. Scientific Reports. 5(1). 16022–16022. 56 indexed citations
10.
Zweier, Christiane, Olaf Rittinger, Ingrid Bader, et al.. (2014). Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 290–301. 20 indexed citations
11.
Casey, Jillian P., Riki Kawaguchi, Hui Sun, et al.. (2011). First implication ofSTRA6mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to theSTRA6phenotype. Human Mutation. 32(12). 1417–1426. 64 indexed citations
12.
Lynch, Sally Ann, et al.. (2011). Case report: Unusual dental morphology in a child with ankyioblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome. European Archives of Paediatric Dentistry. 12(4). 219–223.
13.
Lynch, Sally Ann, et al.. (2008). A Novel Constellation of Cardiac Findings for Kabuki Syndrome: Hypoplastic Left Heart Syndrome and Partial Anomalous Pulmonary Venous Drainage. Pediatric Cardiology. 29(4). 820–822. 13 indexed citations
14.
Mcdonnell, Sharon & Sally Ann Lynch. (2004). Who supports the support workers? Cross-sectional survey of support workers’ experience and views. European Journal of Human Genetics. 12(3). 251–254.
15.
Haniffa, Muzlifah, S. Leech, Sally Ann Lynch, & N. B. Simpson. (2004). NBCCS secondary to an interstitial chromosome 9q deletion. Clinical and Experimental Dermatology. 29(5). 542–544. 15 indexed citations
16.
Ross, Andrew S., et al.. (2000). Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene (vol 66, pg 1504, 2000). UCL Discovery (University College London). 1 indexed citations
17.
Lynch, Sally Ann, et al.. (2000). Autosomal dominant sacral agenesis: Currarino syndrome. Journal of Medical Genetics. 37(8). 561–566. 146 indexed citations
18.
Loughlin, John, Catherine Irven, Zehra Mustafa, et al.. (1998). Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia. Human Mutation. 11(S1). S10–S17. 35 indexed citations
19.
Goodship, JA, Sally Ann Lynch, & Jill M. Brown. (1994). Comparison of facial features of DiGeorge syndrome (DGS) due to deletion 10p13-10pter with DGS due to 22q11 deletion. The American Journal of Human Genetics. 55. 4 indexed citations
20.
Lynch, Sally Ann, et al.. (1991). Antigens of melanocytes and melanoma. Cancer and Metastasis Reviews. 10(2). 141–150. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Peter D. Turnpenny Breakdown of academic impact, for papers by Arthur S. Aylsworth Breakdown of academic impact, for papers by Kenjiro Kosaki Breakdown of academic impact, for papers by Bronwyn Kerr Breakdown of academic impact, for papers by Hülya Kayserili Breakdown of academic impact, for papers by Stephen P. Robertson Breakdown of academic impact, for papers by Domenico Coviello Breakdown of academic impact, for papers by Alan Fryer Breakdown of academic impact, for papers by Marwan Shinawi Breakdown of academic impact, for papers by Marco Seri
Rankless by CCL
2026