Dominic McMullan

5.9k citations

41 papers · 1.7k indexed · h-index 21

Genetics top 2%
Pediatrics, Perinatology and Child Health top 1%
Molecular Biology
Pulmonary and Respiratory Medicine top 10%
Surgery

Co-authors: Mark D. Kilby Eamonn R. Maher Sarah Hillman Arri Coomarasamy Denise Williams Fiona S. Togneri S. Pretlove E. V. Davison
Topics: Genomic variations and chromosomal abnormalities (22 papers)Prenatal Screening and Diagnostics (17 papers)Fetal and Pediatric Neurological Disorders (9 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Cancer Research
Journals: SHILAP Revista de lepidopterologíaHuman Molecular Genetics European Journal of Cancer
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 of co-authors of Dominic McMullan

This figure shows the co-authorship network connecting the top 25 collaborators of Dominic McMullan. A scholar is included among the top collaborators of Dominic McMullan 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 Dominic McMullan. Dominic McMullan 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	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 2023 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Derek Lim,Dominic McMullan,Michael Wright,I. Karen Temple,Justin H. Davies,Deborah Mackay	1
2	Exome Sequencing for Prenatal Detection of Genetic Abnormalities in Fetal Ultrasound Anomalies: An Economic Evaluation 2020 ·Fetal Diagnosis and Therapy ·(unknown),E Quinlan-Jones,Dominic McMullan,Eamonn R. Maher,Matthew E. Hurles,Pelham Barton,Mark D. Kilby	13
3	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
4	Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies 2018 ·Genetics in Medicine ·E Quinlan-Jones,Jenny Lord,Denise Williams,(unknown),Tamás Marton,Ruth Y. Eberhardt,Gabriele Rinck,Elena Prigmore,Rebecca Keelagher,Dominic McMullan,Eamonn R. Maher,Matthew E. Hurles,Mark D. Kilby	41
5	Genomic complexity of urothelial bladder cancer revealed in urinary cfDNA 2016 ·European Journal of Human Genetics ·Fiona S. Togneri,Douglas G. Ward,Joseph Foster,Adam Devall,(unknown),(unknown),(unknown),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	100
6	Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders 2016 ·Human Genetics ·Richard Holt,Sı̇bel Aylı̇n Uğur İşerı̇,(unknown),Dorine A. Bax,(unknown),(unknown),Suzanne Broadgate,R. C. Dunn,(unknown),Yvonne Wallis,Dominic McMullan,Caroline Mackie Ogilvie,Dianne Gerrelli,(unknown),Nicola Ragge	9
7	Cross-laboratory validation of the OncoScan® FFPE Assay, a multiplex tool for whole genome tumour profiling 2015 ·BMC Medical Genomics ·Joseph Foster,Assa Oumie,Fiona S. Togneri,(unknown),(unknown),Morag Taylor,Emma Tinkler‐Hundal,Katie Southward,(unknown),(unknown),Iris Halfpenny,Dominic McMullan,Philip Quirke,Katherine E. Keating,Mike Griffiths,Karen G. Spink,Fiona Brew	71
8	Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound 2014 ·Human Molecular Genetics ·Keren Carss,Sarah Hillman,Vijaya Parthiban,Dominic McMullan,Eamonn R. Maher,Mark D. Kilby,(unknown)	128
9	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
10	How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings? 2013 ·The Journal of Maternal-Fetal & Neonatal Medicine ·Sarah Hillman,Dominic McMullan,Lee Silcock,Eamonn R. Maher,Mark D. Kilby	19
11	TBX5 intragenic duplication: a family with an atypical Holt–Oram syndrome phenotype 2012 ·European Journal of Human Genetics ·Chirag Patel,Lee Silcock,Dominic McMullan,Louise Brueton,Helen Cox	39
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	Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome 2011 ·European Journal of Human Genetics ·Chirag Patel,Lisa Cooper‐Charles,Dominic McMullan,(unknown),Val Davison,Jenny Morton	59
14	Copy number profiling in von hippel‐lindau disease renal cell carcinoma 2011 ·Genes Chromosomes and Cancer ·Salwati Shuib,Wenbin Wei,(unknown),Mark R. Morris,Dominic McMullan,Eleanor Rattenberry,Esther Meyer,Patrick H. Maxwell,Takeshi Kishida,Masahiro Yao,Farida Latif,Eamonn R. Maher	14
15	Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta‐analysis 2010 ·Ultrasound in Obstetrics and Gynecology ·Sarah Hillman,S. Pretlove,Arri Coomarasamy,Dominic McMullan,E. V. Davison,Eamonn R. Maher,Mark D. Kilby	176
16	Molecular characterisation of a recurrent, semi‐cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia 2010 ·British Journal of Haematology ·Nicola Foster,Kajsa Paulsson,Mark Sales,Joan Cunningham,Michael J. Groves,(unknown),(unknown),(unknown),Dominic McMullan,Mike Griffiths,Norman Pratt,Sudhir Tauro	19
17	Design and validation of a metabolic disorder resequencing microarray (BRUM1) 2010 ·Human Mutation ·Christopher K Bruce,(unknown),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	13
18	Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome) 2009 ·American Journal of Medical Genetics Part A ·Salwati Shuib,Dominic McMullan,Eleanor Rattenberry,(unknown),Fatimah Rahman,Malgorzata Zatyka,Cyril Chapman,Fiona MacDonald,Farida Latif,Val Davison,Eamonn R. Maher	76
19	Multilocus loss of heterozygosity allelotypes identify a genetic pathway associated with progression from low to high stage disease in neuroblastoma 2006 ·European Journal of Cancer ·Shaheen Chughtai,(unknown),Pramila Ramani,Sara Dyer,(unknown),Dominic McMullan,Val Davison,Carmel McConville	3
20	Molecular cytogenetic characterization of two non-MYCN amplified neuroblastoma cell lines with complex t(11;17) 2001 ·Cancer Genetics and Cytogenetics ·Carmel McConville,Sara Dyer,(unknown),M E Oude Luttikhuis,Dominic McMullan,(unknown),Pramila Ramani,(unknown),Bruce Morland	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) and Fetal and Pediatric Neurological Disorders (9 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. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and European Journal of Cancer.

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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