Jonathan J. Waters

1.5k citations

32 papers · 1.0k indexed · h-index 17

Impact in

Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Genetics top 5%
- Genomic variations and chromosomal abnormalities

Papers in

Pediatrics, Perinatology and Child Health 14
- Prenatal Screening and Diagnostics 14
- Fetal and Pediatric Neurological Disorders 3
Genetics 16
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 3

Co-authors: Lyn S. Chitty Isabelle Lavenir E Nacheva Terence H. Rabbitts Thomas Boehm A. Förster Richard Baer Caroline Mackie Ogilvie
Journals: Prenatal Diagnosis (8 papers)The EMBO Journal (2 papers)British Journal of Haematology (1 paper)Journal of Cellular Biochemistry (1 paper)American Journal of Obstetrics and Gynecology (1 paper)
Partner nations: United Kingdom United States Australia

In The Last Decade

Jonathan J. Waters

32 papers receiving 955 citations

Peers

Countries citing papers authored by Jonathan J. Waters

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan J. Waters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan J. Waters. 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 Jonathan J. Waters. The network helps show where Jonathan J. Waters may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Jonathan J. Waters, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jonathan J. Waters Line = papers co-authored together Jonathan J. Waters links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation Frontiers in Cellular Neuroscience ·Thomas Parzefall, 慎一郎西田, Maude Chenevard, Gehad Osama Fawzy Sayed, Franco Laccone, Julia Eckl‐Dorna, Jonathan J. Waters, Markus Schreiner, Sami S. Amr, Emma Ashton, Marie-Caline Z Abadjian, Wolfgang Gstœttner, Klemens Frei, Trevor Lucas	2020	5
2	Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy Molecular Syndromology ·Antonietta Coppola, Deborah Morrogh, Madison A. Hooper, Simona Balestrini, Laura Hernández-Hernández, S. Krithika, Josemir W. Sander, Jonathan J. Waters, Sanjay M. Sisodiya	2017	4
3	Trisomy 21 Mid-Trimester Amniotic Fluid Induced Pluripotent Stem Cells Maintain Genetic Signatures During Reprogramming: Implications for Disease Modeling and Cryobanking Cellular Reprogramming ·Caterina Pipino, Sayandip Mukherjee, Anna L. David, Michael P. Blundell, Steven W. Shaw, H.H.K. Alcantara, Panicos Shangaris, Jonathan J. Waters, Nur Ania Fitrianti, Marina Cavazzana, Gustavo Mostoslavsky, Assunta Pandolfi, Agostino Pierro, Pascale V. Guillot, Adrian J. Thrasher, Paolo De Coppi	2014	10
4	The idic(15) syndrome: Expanding the phenotype American Journal of Medical Genetics Part A ·Anna Prancheva, Rodger Palmer, Jonathan J. Waters, Matthias J. Koepp, Raoul C. M. Hennekam, Sanjay M. Sisodiya	2012	3
5	Array comparative genomic hybridization: Results from an adult population with drug-resistant epilepsy and co-morbidities European Journal of Medical Genetics ·Anna Prancheva, Phan, Rodger Palmer, Jonathan J. Waters, Nicholas Lench, Caroline Mackie Ogilvie, Dalia Kasperavičiūtė, Lina Nashef, Sanjay M. Sisodiya	2012	24
6	Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome Pediatric Nephrology ·Janna Kenny, Melissa Lees, Susan Drury, Angela Barnicoat, William van’t Hoff, Rodger Palmer, Deborah Morrogh, Jonathan J. Waters, Nicholas Lench, Detlef Böckenhauer	2011	24
7	QF‐PCR as a stand‐alone test for prenatal samples: the first 2 years' experience in the London region Prenatal Diagnosis ·Alison Hills, Celia Donaghue, Jonathan J. Waters, Vânia Filipe Magalhães, Caroline Sullivan, Abhijit Kulkarni, Zoe Docherty, Kathy Mann, Caroline Mackie Ogilvie	2010	57
8	Complete discrepancy between QF‐PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS Prenatal Diagnosis ·Jonathan J. Waters, Kathy Mann, Беспалова Екатерина Викторовна, Caroline Mackie Ogilvie, Celia Donaghue, Xue Jiansheng, Alison Hills, Tracey L. Adams, Samantha R. Gardner	2007	27
9	Complete discrepancy between abnormal fetal karyotypes predicted by QF‐PCR rapid testing and karyotyped cultured cells in a first‐trimester CVS Prenatal Diagnosis ·Jonathan J. Waters, 亜由美伊坂, Lisa J. Levett, Stuart Liddle, Joschua Wüthrich	2006	14
10	Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational study BMJ ·Lyn S. Chitty, Karl Oliver Kagan, Francisca S. Molina, Jonathan J. Waters, K. H. Nicolaides	2006	53
11	The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing BJOG An International Journal of Obstetrics & Gynaecology ·Caroline Mackie Ogilvie, Alison Lashwood, Lyn S. Chitty, Jonathan J. Waters, Paul N. Scriven, Frances Flinter	2005	51
12	Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second‐trimester amniocenteses Prenatal Diagnosis ·Wing Cheong Leung, Jonathan J. Waters, Lyn S. Chitty	2004	39
13	Prenatal screening for Down syndrome in England and Wales and population-based birth outcomes American Journal of Obstetrics and Gynecology ·Rebecca Smith‐Bindman, Philip Chu, Peter Bacchetti, Jonathan J. Waters, David Mutton, Eva Alberman	2003	19
14	The sequential analysis of trisomy 12 in B‐cell chronic lymphocytic leukaemia British Journal of Haematology ·Ελεονώρα Θλιβίτου, Nicola Bienz, Jeffrey R. Neilson, Renylda Reta, Jonathan J. Waters, D Milligan, Chris Fegan	1999	11
15	Chapter 24 Hippocampal grafts derived from embryonic trisomy 16 mice exhibit amyloid (A4) and neurofibrillary pathology Progress in brain research ·Sarah‐Jane Richards, Jonathan J. Waters, Derek C. Rogers, Fran L. Martel, Dennis R. Sparkman, Charles L. White, Konrad Beyreuther, Colin L. Masters, Stephen B. Dunnett	1990	12
16	Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratio Prenatal Diagnosis ·Jonathan J. Waters, Malcolm Ferguson-Smith, KF Kreitner, Gupt., SV Hodgson	1990	3
17	Trisomy 20q caused by der (X)t(X;20)(q28;q11.2) American Journal of Medical Genetics ·Jonathan J. Waters, Svetlana V. Keschtova, David A. Aitken, B C Davison	1990	12
18	Frequency and extent of allelic loss in the short arm of chromosome 3 in nonsmall‐cell lung cancer Genes Chromosomes and Cancer ·Pamela Rabbitts, Jenny Douglas, Maria C. Daly, Vasi Sundaresan, Sınan Sabit Kocabeyoğlu, M R Zivari, Frank C. Wells, Donna G. Albertson, Jonathan J. Waters, Jonas Bergh	1989	51
19	Cytogenetic abnormalities in human small cell lung carcinoma: Cell lines characterized for myc gene amplification Cancer Genetics and Cytogenetics ·Jonathan J. Waters, Myriam Nait Ajjou, P R Twentyman, N M Bleehen, Pamela Rabbitts	1988	29
20	A scanning electron microscopy study of double minutes from a human tumour cell line Cytogenetic and Genome Research ·R. Pizzatto, Jonathan J. Waters, Christine J. Harrison	1987	10

About Jonathan J. Waters

Jonathan J. Waters is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Infectious Diseases, Developmental Neuroscience and Molecular Biology, having authored 32 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (14 papers), Parvovirus B19 Infection Studies (5 papers), Congenital heart defects research (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Chromosomal and Genetic Variations (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (410 citations), Genetics (439 citations), Hematology (127 citations), Genetics (58 citations) and Molecular Biology (362 citations). Jonathan J. Waters has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Lyn S. Chitty, Isabelle Lavenir, E Nacheva, Terence H. Rabbitts, Thomas Boehm, A. Förster, Richard Baer, Caroline Mackie Ogilvie, Pamela Rabbitts and John A. Crolla. Their work appears in journals such as Prenatal Diagnosis, The EMBO Journal, British Journal of Haematology, Journal of Cellular Biochemistry and American Journal of Obstetrics and Gynecology.

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