Mary O’Driscoll

1.7k citations

20 papers · 390 indexed · h-index 10

Co-authors: Graeme C. Black William B. Dobyns Elliott H. Sherr Jill Clayton‐Smith Eamonn R. Maher Patrick S. Parfrey Jane Green Peter J. Bridge
Topics: Fetal and Pediatric Neurological Disorders (4 papers)Mitochondrial Function and Pathology (3 papers)Genetic Neurodegenerative Diseases (3 papers)
Cited by: Neurology Pediatrics, Perinatology and Child Health Genetics
Journals: The American Journal of Human Genetics Diseases of the Colon & Rectum Medical Education
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Mary O’Driscoll

18 papers receiving 381 citations

Peers

Countries citing papers authored by Mary O’Driscoll

Since Specialization

Citations

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

Fields of papers citing papers by Mary O’Driscoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary O’Driscoll. 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 Mary O’Driscoll. The network helps show where Mary O’Driscoll may publish in the future.

Co-authorship network of co-authors of Mary O’Driscoll

This figure shows the co-authorship network connecting the top 25 collaborators of Mary O’Driscoll. A scholar is included among the top collaborators of Mary O’Driscoll 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 Mary O’Driscoll. Mary O’Driscoll 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	Myoclonus-dystonia due to novel mutation in the guanine nucleotide-binding protein (GNB1) gene 2025 ·Parkinsonism & Related Disorders ·Duncan Street,(unknown),Teodora Georgieva,(unknown),Suzanne Broadgate,Penny Clouston,Mary O’Driscoll	0
2	Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL 2021 ·Brain Communications ·Neil V. Morgan,Bryndís Yngvadóttir,Mary O’Driscoll,Graeme R. Clark,(unknown),Jose‐Ezequiel Martín,Louise Tee,Evan Reid,Hannah Titheradge,Eamonn R. Maher	11
3	Late-onset ataxia plus syndromes 2020 ·Neurology Clinical Practice ·Duncan Street,Mary O’Driscoll,A. Malcolm R. Taylor,David Nicholl	0
4	27 years of prenatal diagnosis for Huntington disease in the United Kingdom 2018 ·Genetics in Medicine ·Raúl E. Piña-Aguilar,Sheila A Simpson,(unknown),Angus Clarke,David Craufurd,Huw Dorkins,(unknown),Nayana Lahiri,Alison Lashwood,(unknown),Claire Miller,(unknown),Mary O’Driscoll,Oliver Quarrell,D. O. Rae,Mark Strong,(unknown),Peter D. Turnpenny,Zosia Miedzybrodzka	9
5	Comprehensive molecular screening strategy of OCLN in band‐like calcification with simplified gyration and polymicrogyria 2017 ·Clinical Genetics ·Emma M. Jenkinson,John H. Livingston,Mary O’Driscoll,Isabelle Desguerre,Rima Nabbout,Nathalie Boddaert,Gabriela Soares,(unknown),Stefano D’Arrigo,Gillian Rice,Yanick J. Crow	8
6	Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences 2017 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Oliver Quarrell,Angus Clarke,Cecilia Compton,(unknown),Alan Fryer,(unknown),Nayana Lahiri,Rhona MacLeod,Zosia Miedzybrodzka,Patrick J. Morrison,Hannah Musgrave,Mary O’Driscoll,Mark Strong,Martine J. van Belzen,Sascha Vermeer,Corien C. Verschuuren‐Bemelmans,Emilia K. Bijlsma	1
7	Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis 2016 ·The American Journal of Human Genetics ·(unknown),Markus Storbeck,Raoul Heller,Irmgard Hölker,Malavika Hebbar,Anju Shukla,Ólafur Þ. Magnússon,Sebahattin Çırak,Katta M. Girisha,Mary O’Driscoll,Bart Loeys,Brunhilde Wirth	72
8	Contralateral breast cancer in high-risk patients: Identification of risk factors to guide recommendations for contralateral prophylactic mastectomy – A 30-year experience 2013 ·European Journal of Surgical Oncology ·(unknown),Mary O’Driscoll,Munaza Ahmed,Sarah Ingham,Anthony Howell,Fiona Lalloo,D. Gareth Evans	1
9	Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene 2011 ·American Journal of Medical Genetics Part A ·Nathan Osbun,Li Jiang,Mary O’Driscoll,Zoe Strominger,Mari Wakahiro,(unknown),Polina Bukshpun,(unknown),Cailyn H. Spurrell,Wendy Schackwitz,L Pennacchio,William B. Dobyns,Graeme C. Black,Elliott H. Sherr	29
10	Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria 2010 ·The American Journal of Human Genetics ·Mary O’Driscoll,Sarah B. Daly,Jill Urquhart,Graeme C. Black,Daniela T. Pilz,Knut Brockmann,Meriel McEntagart,Ghada M. H. Abdel‐Salam,Maha S. Zaki,Nicole I. Wolf,Roger L. Ladda,Susan L. Sell,Stefano D’Arrigo,Waney Squier,William B. Dobyns,John H. Livingston,Yanick J. Crow	92
11	Cerebellar hypoplasia and Cohen syndrome: A confirmed association 2010 ·American Journal of Medical Genetics Part A ·(unknown),Mirja Somer,Mary O’Driscoll,Kathleen J. Millen,Forbes Manson,Kate Chandler	10
12	Agenesis of the corpus callosum and congenital lymphedema: A novel recognizable syndrome? 2010 ·American Journal of Medical Genetics Part A ·Mary O’Driscoll,Kim Jenny,Sulagna C. Saitta,William B. Dobyns,Karen W. Gripp	2
13	Identification of genomic loci contributing to agenesis of the corpus callosum 2010 ·American Journal of Medical Genetics Part A ·Mary O’Driscoll,Graeme C. Black,Jill Clayton‐Smith,Elliott H. Sherr,William B. Dobyns	53
14	Bilateral camptodactyly and recurrent patellar dislocation: a new sign of 22q11 deletions or an independent dominant disorder? 2008 ·Clinical Dysmorphology ·Mary O’Driscoll,Jill Clayton‐Smith	3
15	Four limb syndactyly, constriction rings and skin tags; amniotic bands or disorganization-like syndrome 2008 ·Clinical Dysmorphology ·Mary O’Driscoll,(unknown),Bronwyn Kerr	12
16	Impact of Gender and Parent of Origin on the Phenotypic Expression of Hereditary Nonpolyposis Colorectal Cancer in a Large Newfoundland Kindred With a Common MSH2 Mutation 2002 ·Diseases of the Colon & Rectum ·Jane Green,Mary O’Driscoll,(unknown),Eamonn R. Maher,Peter J. Bridge,(unknown),Patrick S. Parfrey	47
17	Can medical students contribute to quality assurance programmes in day surgery? 1999 ·Medical Education ·Glenda E. Rudkin,Mary O’Driscoll,(unknown)	4
18	DOES A TEACHING PROGRAMME IN DAY SURGERY IMPACT ON EFFICIENCY AND QUALITY OF CARE? 1997 ·Australian and New Zealand Journal of Surgery ·Glenda E. Rudkin,Mary O’Driscoll,(unknown)	13
19	Observations on the Motor Development of Visually Impaired Children Interpretations from Video Recordings 1989 ·Physiotherapy ·(unknown),Mary O’Driscoll	15
20	A case of neonatal herpes simplex with pneumonia. 1983 ·PubMed ·(unknown),Mary O’Driscoll,(unknown),Stanley Read	8

About Mary O’Driscoll

Mary O’Driscoll is a scholar working on Developmental Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 20 papers that have together received 390 indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Neurology (47 citations), Pediatrics, Perinatology and Child Health (95 citations) and Genetics (87 citations). Mary O’Driscoll has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Graeme C. Black, William B. Dobyns, Elliott H. Sherr, Jill Clayton‐Smith, Eamonn R. Maher, Patrick S. Parfrey, Jane Green, Peter J. Bridge, Raoul Heller and Anju Shukla. Their work appears in journals such as The American Journal of Human Genetics, Diseases of the Colon & Rectum and Medical Education.

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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