Denise Williams

4.7k total citations
38 papers, 1.6k citations indexed

About

Denise Williams is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Denise Williams has authored 38 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 18 papers in Pediatrics, Perinatology and Child Health and 11 papers in Molecular Biology. Recurrent topics in Denise Williams's work include Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (12 papers) and Genomic variations and chromosomal abnormalities (8 papers). Denise Williams is often cited by papers focused on Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (12 papers) and Genomic variations and chromosomal abnormalities (8 papers). Denise Williams collaborates with scholars based in United Kingdom, France and United States. Denise Williams's co-authors include Chiaki Mukai, A. Kuipers, Mark D. Kilby, Danielle I. Young, Marian F. Young, Dominic McMullan, Sarah Hillman, Eamonn R. Maher, Stephanie Allen and Fiona S. Togneri and has published in prestigious journals such as Diabetes, Journal of the American Society of Nephrology and The American Journal of Human Genetics.

In The Last Decade

Denise Williams

38 papers receiving 1.5k citations

Peers

Countries citing papers authored by Denise Williams

Since Specialization

Citations

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

Fields of papers citing papers by Denise Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denise Williams

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Molecular autopsy for fetal structural anomaly: diagnostic and clinical utility of multidisciplinary team approach 2024 ·Ultrasound in Obstetrics and Gynecology ·(unknown), (unknown), Fionnuala Mone, (unknown), (unknown), Stephanie Allen, (unknown), Tamás Marton, Denise Williams	2
2	Prenatal next-generation sequencing in the fetus with congenital malformations: how can we improve clinical utility? 2023 ·American Journal of Obstetrics & Gynecology MFM ·Mark D. Kilby, Siân Morgan, Fionnuala Mone, Denise Williams	5
3	Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation 2022 ·Genes ·(unknown), James Castleman, Stephanie Allen, Denise Williams, Esther Kinning, Mark D. Kilby	12
4	Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies 2021 ·BJOG An International Journal of Obstetrics & Gynaecology ·Fionnuala Mone, (unknown), Denise Williams, Lyn S. Chitty, ER Maher, Mark D. Kilby, (unknown)	29
5	Clinical Service Delivery of Noninvasive Prenatal Diagnosis by Relative Haplotype Dosage for Single-Gene Disorders 2020 ·Journal of Molecular Diagnostics ·Elizabeth Young, (unknown), Amy Gerrish, Michael Parks, (unknown), Samuel Clokie, (unknown), (unknown), Denise Williams, Trevor Cole, Stephanie Allen	18
6	Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases 2019 ·Prenatal Diagnosis ·(unknown), Susan Hamilton, Fionnuala Mone, Ka Wang Cheung, Fiona S. Togneri, R. Katie Morris, E Quinlan-Jones, Denise Williams, Stephanie Allen, Dominic McMullan, Mark D. Kilby	20
7	Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics Laboratory 2019 ·Genetics Research ·Fiona S. Togneri, Mark D. Kilby, Elizabeth Young, (unknown), Denise Williams, Mike Griffiths, Stephanie Allen	6
8	The first antenatal diagnosis of KBG syndrome: a microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD 11 associated with the disorder 2017 ·Clinical Case Reports ·Victoria Hodgetts Morton, E Quinlan-Jones, (unknown), Denise Williams, (unknown), Tamás Marton, R. Katie Morris	4
9	Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage 2017 ·European Journal of Human Genetics ·Michael Parks, (unknown), (unknown), Siobhán Cleary, Samuel Clokie, (unknown), Denise Williams, Trevor Cole, Fiona MacDonald, Mike Griffiths, Stephanie Allen	74
10	EVALUATION OF VISUAL FUNCTION AND NEEDS IN ADULT PATIENTS WITH BARDET–BIEDL SYNDROME 2014 ·Retina ·Alastair K. Denniston, Philip L. Beales, (unknown), Peter Good, (unknown), Lukas Foggensteiner, Denise Williams, Marie Tsaloumas	30
11	Additional information from chromosomal microarray analysis ( CMA ) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta‐analysis 2013 ·BJOG An International Journal of Obstetrics & Gynaecology ·(unknown), Sarah Hillman, R. Katie Morris, Dominic McMullan, Denise Williams, Arri Coomarasamy, Mark D. Kilby	80
12	Microarray comparative genomic hybridization in prenatal diagnosis: a review 2012 ·Ultrasound in Obstetrics and Gynecology ·Sarah Hillman, Dominic McMullan, Denise Williams, Eamonn R. Maher, Mark D. Kilby	23
13	Anti-Listeria bacteriocin-producing bacteria from raw ewe’s milk in northern Greece 2011 ·Journal of Applied Microbiology ·(unknown), Denise Williams	3
14	Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome) 2010 ·The American Journal of Human Genetics ·Esther Meyer, Christopher J. Ricketts, Neil V. Morgan, Mark R. Morris, Shanaz Pasha, Louise Tee, Fatimah Rahman, Anne Bazin, Bettina Bessières, Pierre Déchelotte, (unknown), Mudher Al‐Adnani, Tamás Marton, David Tannahill, Richard C. Trembath, Catherine Fallet‐Bianco, P. Cox, Denise Williams, Eamonn R. Maher	46
15	Anti-Listeria bacteriocin-producing bacteria from raw ewe’s milk in northern Greece 2010 ·Journal of Applied Microbiology ·(unknown), Denise Williams	18
16	Recurrent hydatidiform moles 2010 ·European Journal of Obstetrics & Gynecology and Reproductive Biology ·Denise Williams, Victoria Hodgetts Morton, Janesh Gupta	34
17	Acclimation during space flight: effects on human physiology 2009 ·Canadian Medical Association Journal ·Denise Williams, A. Kuipers, Chiaki Mukai, (unknown)	233
18	The space-flight environment: the International Space Station and beyond 2009 ·Canadian Medical Association Journal ·(unknown), A. Kuipers, Chiaki Mukai, Denise Williams	161
19	A Phenotypic Variant of Knobloch Syndrome 2008 ·Ophthalmic Genetics ·(unknown), G R Kirkby, Denise Williams, John R. Ainsworth	15
20	Conjugative plasmid transfer from Escherichia coli to Clostridium acetobutylicum 1990 ·Journal of General Microbiology ·Denise Williams, Danielle I. Young, Marian F. Young	135

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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