Lyn S. Chitty

20.5k total citations · 3 hit papers
309 papers, 12.1k citations indexed

About

Lyn S. Chitty is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases. According to data from OpenAlex, Lyn S. Chitty has authored 309 papers receiving a total of 12.1k indexed citations (citations by other indexed papers that have themselves been cited), including 212 papers in Pediatrics, Perinatology and Child Health, 91 papers in Genetics and 59 papers in Infectious Diseases. Recurrent topics in Lyn S. Chitty's work include Prenatal Screening and Diagnostics (185 papers), Fetal and Pediatric Neurological Disorders (88 papers) and Parvovirus B19 Infection Studies (59 papers). Lyn S. Chitty is often cited by papers focused on Prenatal Screening and Diagnostics (185 papers), Fetal and Pediatric Neurological Disorders (88 papers) and Parvovirus B19 Infection Studies (59 papers). Lyn S. Chitty collaborates with scholars based in United Kingdom, United States and India. Lyn S. Chitty's co-authors include Douglas G. Altman, Melissa Hill, Celine Lewis, Charles H. Rodeck, S. Campbell, Angela N. Barrett, Neil J. Sebire, Nicholas Wald, Jocelyn Walters and Allan Hackshaw and has published in prestigious journals such as The Lancet, Circulation and SHILAP Revista de lepidopterología.

In The Last Decade

Lyn S. Chitty

302 papers receiving 11.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Spina bifida

2015 395 citations Lyn S. Chitty et al. profile →
Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis

2022 118 citations Rhiannon Mellis, Elizabeth Scotchman et al. Prenatal Diagnosis profile →
Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies

2023 58 citations Lisa Hui, Lyn S. Chitty et al. Prenatal Diagnosis profile →

Peers

Countries citing papers authored by Lyn S. Chitty

Since Specialization

Citations

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

Fields of papers citing papers by Lyn S. Chitty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lyn S. Chitty. 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 Lyn S. Chitty. The network helps show where Lyn S. Chitty may publish in the future.

Co-authorship network of co-authors of Lyn S. Chitty

This figure shows the co-authorship network connecting the top 25 collaborators of Lyn S. Chitty. A scholar is included among the top collaborators of Lyn S. Chitty 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 Lyn S. Chitty. Lyn S. Chitty 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	Are People From Black Communities Proportionately Represented in UK and US Studies Examining Views on Screening and Diagnostic Genetic Testing in Pregnancy? A Scoping Review 2025 ·BJOG An International Journal of Obstetrics & Gynaecology ·Michelle Peter, (unknown), Celine Lewis, Lyn S. Chitty, Melissa Hill	1
2	Preferences for coordinated care for rare diseases: discrete choice experiment 2024 ·Orphanet Journal of Rare Diseases ·Stephen Morris, Holly Walton, Amy Simpson, (unknown), Lara Bloom, Amy Hunter, Angus I. G. Ramsay, Naomi Fulop, Lyn S. Chitty, Joe Kai, Alastair Sutcliffe, (unknown), Larissa Kerecuk, Christine A. Taylor, (unknown)	2
3	Evaluating the Implementation of the Rapid Prenatal Exome Sequencing Service in England 2024 ·Public Health Genomics ·Holly Walton, (unknown), Michelle Peter, (unknown), Rhiannon Mellis, Stephanie Allen, Naomi Fulop, Lyn S. Chitty, Melissa Hill	3
4	Parental Somatic Mosaicism Detected During Prenatal Diagnosis 2024 ·Prenatal Diagnosis ·Natalie Chandler, Elizabeth Scotchman, Fiona McKay, Vijaya Ramachandran, Lyn S. Chitty	0
5	Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals 2023 ·Orphanet Journal of Rare Diseases ·Holly Walton, (unknown), Amy Simpson, Lara Bloom, Lyn S. Chitty, Naomi Fulop, Amy Hunter, Jennifer Jones, Joe Kai, Larissa Kerecuk, (unknown), (unknown), (unknown), Angus I. G. Ramsay, Alastair Sutcliffe, Christine Taylor, Stephen Morris	6
6	Non‐invasive fetal genotyping for maternal alleles with droplet digital PCR: A comparative study of analytical approaches 2023 ·Prenatal Diagnosis ·Joseph Shaw, Elizabeth Scotchman, (unknown), (unknown), (unknown), (unknown), Tristan Snowsill, Lyn S. Chitty, Natalie Chandler	8
7	Co-ordinated care for people affected by rare diseases: the CONCORD mixed-methods study 2022 ·SHILAP Revista de lepidopterología ·Stephen Morris, Emma Hudson, Lara Bloom, Lyn S. Chitty, Naomi Fulop, Amy Hunter, Jennifer Jones, Joe Kai, Larissa Kerecuk, (unknown), (unknown), (unknown), (unknown), Angus I. G. Ramsay, Amy Simpson, Alastair Sutcliffe, Christine Taylor, Holly Walton	9
8	Right or wrong? Looking through the retrospectoscope to analyse predictions made a decade ago in prenatal diagnosis and fetal surgery 2020 ·Prenatal Diagnosis ·Lyn S. Chitty, Alessandro Ghidini, Jan Deprest, Tim Van Mieghem, Brynn Levy, Lisa Hui, Diana W. Bianchi	4
9	Development of a measure of genome sequencing knowledge for young people: The kids‐KOGS 2019 ·Clinical Genetics ·Celine Lewis, Bao Sheng Loe, Chris Sidey‐Gibbons, Christine Patch, Lyn S. Chitty, Saskia C. Sanderson	4
10	Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project 2019 ·BMJ Open ·Saskia C. Sanderson, Melissa Hill, Christine Patch, Beverly Searle, Celine Lewis, Lyn S. Chitty	29
11	Preferences for prenatal testing among pregnant women, partners and health professionals. 2018 ·PubMed ·Ida Charlotte Bay Lund, Naja Becher, Olav Bjørn Petersen, Melissa Hill, Lyn S. Chitty, Ida Vogel	15
12	Development of the Knowledge of Genome Sequencing (KOGS) questionnaire 2018 ·Patient Education and Counseling ·Saskia C. Sanderson, Bao Sheng Loe, (unknown), Camila Pires Cremasco Gabriel, Danielle C. Stevenson, Chris Sidey‐Gibbons, Lyn S. Chitty, Celine Lewis	14
13	Uptake, Outcomes, and Costs of Implementing Non-invasive Prenatal Testing for Down Syndrome Into NHS Maternity Care: Prospective Cohort Study in Eight Diverse Maternity Units 2016 ·Obstetrical & Gynecological Survey ·Lyn S. Chitty, D. Wright, Melissa Hill, Talitha I. Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, (unknown), (unknown), (unknown), Jane Fisher, Mark Kroese, Stephen Morris	5
14	Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons 2016 ·The American Journal of Human Genetics ·Brian Harding, (unknown), Séverine Drunat, Omar Soukarieh, Hélène Tubeuf, Lyn S. Chitty, Alain Verloès, Pierre Gressèns, Vincent El Ghouzzi, Sylvie Joriot, Ferdinando Di Cunto, Alexandra Martins, Sandrine Passemard, Stephanie Bielas	47
15	Non‐invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next‐generation sequencing allows for a safer, more accurate, and comprehensive approach 2015 ·Prenatal Diagnosis ·Lyn S. Chitty, Sarah Mason, Angela N. Barrett, Fiona McKay, Nicholas Lench, Rebecca Daley, Lucy Jenkins	112
16	Will the introduction of non-invasive prenatal testing for Down's syndrome undermine informed choice? 2015 ·UCL Discovery (University College London) ·(unknown), (unknown), Melissa Hill, Lyn S. Chitty	1
17	Non‐invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis 2015 ·Prenatal Diagnosis ·Melissa Hill, Philip Twiss, Talitha I. Verhoef, Suzanne Drury, Fiona McKay, Sarah Mason, Lucy Jenkins, Stephen Morris, Lyn S. Chitty	61
18	Diagnostic Accuracy of Routine Antenatal Determination of Fetal RHD Status Across Gestation 2015 ·Obstetrical & Gynecological Survey ·Lyn S. Chitty, Kirstin Finning, Angela Wade, Peter Soothill, Bill Martin, (unknown), Geoff Daniels, Edwin Massey	2
19	Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study (vol 382, pg 223, 2013) 2013 ·UCL Discovery (University College London) ·Sudhin Thayyil, Neil J. Sebire, Lyn S. Chitty	4
20	Prospective Register of Outcomes of Free-fetal DNA testing (PROOF) - results of the first year's audit 2007 ·UCL Discovery (University College London) ·Lyn S. Chitty, Geoff Daniels, K. Finning, (unknown), (unknown), Peter Martin, Christopher Meaney, Gail Norbury, (unknown)	11

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