Dominic McMullan

5.9k citations

41 papers · 1.7k indexed · h-index 21

Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics 17
- Fetal and Pediatric Neurological Disorders 9
Genetics top 2%
- Genomic variations and chromosomal abnormalities 22
- Genomics and Rare Diseases 7
Cancer Research
- Cancer Genomics and Diagnostics 4
- Cancer, Hypoxia, and Metabolism 3
Hematology top 10%
Molecular Biology
- Congenital heart defects research 6
Neurology
- Neuroblastoma Research and Treatments 4

Co-authors: Mark D. Kilby Eamonn R. Maher Sarah Hillman Arri Coomarasamy Denise Williams Fiona S. Togneri S. Pretlove E. V. Davison
Cited by: Pediatrics, Perinatology and Child Health Genetics Cancer Research
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Dominic McMullan

41 papers receiving 1.7k citations

Peers

Countries citing papers authored by Dominic McMullan

Since Specialization

Citations

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

Fields of papers citing papers by Dominic McMullan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Dominic McMullan, 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 Dominic McMullan Line = papers co-authored together Dominic McMullan links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A case of mosaic deletion of paternally‐inherited PLAGL1 and two cases of upd(6)mat add to evidence for PLAGL1 under‐expression as a cause of growth restriction Ahmed Alhendi,Gabriella Gazdagh,Derek Lim,Dominic McMullan,Michael Wright,I. Karen Temple,Justin H. Davies,Deborah Mackay	2023	1
2	Exome Sequencing for Prenatal Detection of Genetic Abnormalities in Fetal Ultrasound Anomalies: An Economic Evaluation Shahela Kodabuckus,E Quinlan-Jones,Dominic McMullan,Eamonn R. Maher,Matthew E. Hurles,Pelham Barton,Mark D. Kilby	2020	13
3	Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases Hsu Phern Chong,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	2019	20
4	Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies E Quinlan-Jones,Jenny Lord,Denise Williams,S. Hamilton,Tamás Marton,Ruth Y. Eberhardt,Gabriele Rinck,Elena Prigmore,Rebecca Keelagher,Dominic McMullan,Eamonn R. Maher,Matthew E. Hurles,Mark D. Kilby	2018	41
5	Genomic complexity of urothelial bladder cancer revealed in urinary cfDNA Fiona S. Togneri,Douglas G. Ward,Joseph Foster,Adam Devall,Paula Wojtowicz,Sofia Alyas,Fabiana Ramos Vasques,Assa Oumie,Nicholas D. James,Kar Keung Cheng,Maurice P. Zeegers,Nayneeta Deshmukh,Brendan O’Sullivan,Philippe Tanière,Karen G. Spink,Dominic McMullan,Mike Griffiths,Richard T. Bryan	2016	100
6	Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders Richard Holt,Sı̇bel Aylı̇n Uğur İşerı̇,Alex Wyatt,Dorine A. Bax,D. Gold Diaz,C. Santos,Suzanne Broadgate,R. C. Dunn,Jonathan Bruty,Yvonne Wallis,Dominic McMullan,Caroline Mackie Ogilvie,Dianne Gerrelli,Y. Zhang,Nicola Ragge	2016	9
7	Cross-laboratory validation of the OncoScan® FFPE Assay, a multiplex tool for whole genome tumour profiling Joseph Foster,Assa Oumie,Fiona S. Togneri,Fabiana Ramos Vasques,Debra Hau,Morag Taylor,Emma Tinkler‐Hundal,Katie Southward,Paul Medlow,Keith McGreeghan-Crosby,Iris Halfpenny,Dominic McMullan,Philip Quirke,Katherine E. Keating,Mike Griffiths,Karen G. Spink,Fiona Brew	2015	71
8	Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound Keren Carss,Sarah Hillman,Vijaya Parthiban,Dominic McMullan,Eamonn R. Maher,Mark D. Kilby,M. E. Hurles	2014	128
9	Additional information from chromosomal microarray analysis ( CMA ) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta‐analysis RK Dhillon,Sarah Hillman,R. Katie Morris,Dominic McMullan,Denise Williams,Arri Coomarasamy,Mark D. Kilby	2013	80
10	How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings? Sarah Hillman,Dominic McMullan,Lee Silcock,Eamonn R. Maher,Mark D. Kilby	2013	19
11	TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype Chirag Patel,Lee Silcock,Dominic McMullan,Louise Brueton,Helen Cox	2012	39
12	Microarray comparative genomic hybridization in prenatal diagnosis: a review Sarah Hillman,Dominic McMullan,Denise Williams,Eamonn R. Maher,Mark D. Kilby	2012	23
13	Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome Chirag Patel,Lisa Cooper‐Charles,Dominic McMullan,Judith Walker,Val Davison,Jenny Morton	2011	59
14	Copy number profiling in von hippel‐lindau disease renal cell carcinoma Salwati Shuib,Wenbin Wei,Hariom Sur,Mark R. Morris,Dominic McMullan,Eleanor Rattenberry,Esther Meyer,Patrick H. Maxwell,Takeshi Kishida,Masahiro Yao,Farida Latif,Eamonn R. Maher	2011	14
15	Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta‐analysis Sarah Hillman,S. Pretlove,Arri Coomarasamy,Dominic McMullan,E. V. Davison,Eamonn R. Maher,Mark D. Kilby	2010	176
16	Molecular characterisation of a recurrent, semi‐cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia Nicola Foster,Kajsa Paulsson,Mark Sales,Joan Cunningham,Michael J. Groves,Nigel O’Connor,Suriya Begum,Tracy Stubbs,Dominic McMullan,Mike Griffiths,Norman Pratt,Sudhir Tauro	2010	19
17	Design and validation of a metabolic disorder resequencing microarray (BRUM1) Christopher K Bruce,Matthew Smith,Fatima Rahman,Zhifeng Liu,Dominic McMullan,Sarah Ball,Jane Hartley,Marian A. Kroos,Lesley Heptinstall,Arnold Reuser,Arndt Rolfs,Christian J. Hendriksz,Déirdre Kelly,Timothy Barrett,Fiona MacDonald,Eamonn R. Maher,Paul Gissen	2010	13
18	Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome) Salwati Shuib,Dominic McMullan,Eleanor Rattenberry,Richard M. Barber,Fatimah Rahman,Malgorzata Zatyka,Cyril Chapman,Fiona MacDonald,Farida Latif,Val Davison,Eamonn R. Maher	2009	76
19	Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma Shaheen Chughtai,Tracey Genus,Pramila Ramani,Sara Dyer,Judy E. Powell,Dominic McMullan,Val Davison,Carmel McConville	2006	3
20	Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17) Carmel McConville,Sara Dyer,S. A. Rees,M E Oude Luttikhuis,Dominic McMullan,Susan J. Vickers,Pramila Ramani,Darren Redfern,Bruce Morland	2001	8

About Dominic McMullan

Dominic McMullan is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 41 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (9 papers), Genomics and Rare Diseases (7 papers), Congenital heart defects research (6 papers), Neuroblastoma Research and Treatments (4 papers), Cancer Genomics and Diagnostics (4 papers) and Cancer, Hypoxia, and Metabolism (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (801 citations), Genetics (848 citations) and Cancer Research (157 citations). Dominic McMullan has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Mark D. Kilby, Eamonn R. Maher, Sarah Hillman, Arri Coomarasamy, Denise Williams, Fiona S. Togneri, S. Pretlove, E. V. Davison, Ronald J. Wapner and Pramila Ramani.

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