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P. Morrison · SciRah

Researcher profile · Semantic Scholar

P. Morrison

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P. Morrison — researcher profile on SciRah

h-index: 46
Works: 287
Citations: 7,598

Most-cited papers

Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial
J. Burn, H. Sheth, F. Elliott, Linda Reed +30 more
2020The Lancet331 citations Open access
Semantic Scholar
Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD
Katrina A. Andrews, D. Ascher, Douglas E. V. Pires, D. Barnes +33 more
2018Journal of Medical Genetics216 citations Open access
Semantic Scholar
Germline FH mutations presenting with pheochromocytoma.
Graeme Clark, M. Sciacovelli, E. Gaude, D. Walsh +9 more
2014Journal of Clinical Endocrinology and Metabolism174 citations Open access
Semantic Scholar
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
A. Osorio, R. Milne, Karoline B. Kuchenbaecker, Tereza Vaclová +193 more
2014PLoS Genetics123 citations Open access
Semantic Scholar
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study.
M. Movahedi, D. Bishop, F. Macrae, J. Mecklin +21 more
2015Journal of Clinical Oncology114 citations Open access
Semantic Scholar
Clinical and genetic characterization of leukoencephalopathies in adults
David S. Lynch, Anderson Rodrigues Brandão de Paiva, Wei Zhang, E. Bugiardini +25 more
2017Brain : a journal of neurology87 citations Open access
Semantic Scholar
Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative effects
F. Hannan, S. Howles, A. Rogers, T. Cranston +32 more
2015Human Molecular Genetics86 citations Open access
Semantic Scholar
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
L. Schottlaender, R. Abeti, Z. Jaunmuktane, C. Macmillan +83 more
2020American Journal of Human Genetics79 citations Open access
Semantic Scholar
Variation in the Risk of Colorectal Cancer for Lynch Syndrome: A retrospective family cohort study
Aung Ko Win, J. Dowty, J. Reece, Grant Lee +208 more
2021The Lancet Oncology64 citations Open access
Semantic Scholar
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
Karoline B. Kuchenbaecker, S. Neuhausen, M. Robson, D. Barrowdale +206 more
2014Breast Cancer Research63 citations Open access
Semantic Scholar
Clinical experience in the screening and management of a large kindred with familial isolated pituitary adenoma due to an aryl hydrocarbon receptor interacting protein (AIP) mutation.
F. Williams, S. Hunter, L. Bradley, H. Chahal +9 more
2014Journal of Clinical Endocrinology and Metabolism59 citations
Semantic Scholar
Significant Benefits of AIP Testing and Clinical Screening in Familial Isolated and Young-onset Pituitary Tumors
P. Marques, F. Caimari, Laura C. Hernández-Ramírez, D. Collier +279 more
2020Journal of Clinical Endocrinology and Metabolism58 citations Open access
Semantic Scholar
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing.
P. Salpea, A. Horvath, E. London, F. Faucz +16 more
2014Journal of Clinical Endocrinology and Metabolism56 citations Open access
Semantic Scholar
The Impact of Neurofibromatosis Type 1 on the Health and Wellbeing of Australian Adults
H. Crawford, Belinda Barton, M. Wilson, Y. Berman +3 more
2015Journal of Genetic Counseling54 citations Open access
Semantic Scholar
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
P. Møller, T. Seppälä, J. Dowty, Saskia Haupt +153 more
2022Hereditary Cancer in Clinical Practice53 citations Open access
Semantic Scholar
Epidemiology, clinical features, and genetics of multiple endocrine neoplasia type 2B in a complete population.
A. Znaczko, D. Donnelly, P. Morrison
2014The Oncologist44 citations Open access
Semantic Scholar
Cancer Prevention with Resistant Starch in Lynch syndrome patients in the CAPP2 Randomised Placebo Controlled Trial: planned 10-year follow-up
J. Mathers, F. Elliott, F. Macrae, J. Mecklin +18 more
2022Cancer Prevention Research42 citations Open access
Semantic Scholar
Spinocerebellar ataxias.
B. Soong, P. Morrison
2018Handbook of Clinical Neurology39 citations
Semantic Scholar
Two recurrent mutations are associated with GNE myopathy in the North of Britain
A. Chaouch, K. Brennan, J. Hudson, C. Longman +19 more
2014Journal of Neurology Neurosurgery & Psychiatry38 citations Open access
Semantic Scholar
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M. M. Lakeman, A. J. van den Broek, J. A. Vos, D. Barnes +210 more
2021Genetics in Medicine37 citations Open access
Semantic Scholar
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, M. Lush, J. Beesley, T. O'Mara +388 more
2021Nature Communications37 citations Open access
Semantic Scholar
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores
D. Barnes, Valentina Silvestri, Goska Leslie, L. McGuffog +160 more
2021Journal of the National Cancer Institute36 citations Open access
Semantic Scholar
The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations
M. Terry, Yu-Yan Liao, K. Kast, A. Antoniou +51 more
2018JNCI Cancer Spectrum35 citations Open access
Semantic Scholar
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
S. Blein, C. Bardel, Vincent Danjean, L. McGuffog +202 more
2015Breast Cancer Research33 citations Open access
Semantic Scholar
Germline ESR2 mutation predisposes to medullary thyroid carcinoma and causes up-regulation of RET expression.
J. Smith, Martin L Read, J. Hoffman, Rachel M. Brown +24 more
2016Human Molecular Genetics32 citations Open access
Semantic Scholar
Association of prolactin receptor (PRLR) variants with prolactinomas
C. Gorvin, P. Newey, A. Rogers, V. Stokes +11 more
2018Human Molecular Genetics29 citations Open access
Semantic Scholar
Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
P. Peterlongo, J. Chang-Claude, K. Moysich, A. Rudolph +197 more
2014Cancer Epidemiology, Biomarkers and Prevention29 citations Open access
Semantic Scholar
Increased Population Risk of AIP‐Related Acromegaly and Gigantism in Ireland
S. Radian, Y. Diekmann, P. Gabrovska, B. Holland +44 more
2016Human Mutation26 citations Open access
Semantic Scholar
Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated Care
Nicholas M. P. Annear, R. Appleton, Zahabiyah Bassi, R. Bhatt +20 more
2019Frontiers in Neurology25 citations Open access
Semantic Scholar
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders
Fatima Abdelfattah, A. Kariminejad, Anne-Karin Kahlert, P. Morrison +25 more
2020Human Mutation21 citations Open access
Semantic Scholar
Interventions to improve psychosocial well-being in female BRCA-mutation carriers following risk-reducing surgery.
L. Jeffers, J. Reid, D. Fitzsimons, P. Morrison +1 more
2017Cochrane Database of Systematic Reviews21 citations Open access
Semantic Scholar
MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism
V. Chelban, M. Carecchio, Gillian Rea, A. Bowirrat +22 more
2020Neurology: Genetics20 citations Open access
Semantic Scholar
Multifocal breast cancers are more prevalent in BRCA2 versus BRCA1 mutation carriers
A. McCrorie, Susannah Ashfield, A. Begley, C. Mcilmunn +9 more
2019medRxiv19 citations Open access
Semantic Scholar
A quick reference guide for rare disease: supporting rare disease management in general practice.
A. Crowe, H. McAneney, P. Morrison, M. Cupples +1 more
2020The British journal of general practice : the journal of the Royal College of General Practitioners18 citations Open access
Semantic Scholar
Risks of breast or ovarian cancer in BRCA1 or BRCA2 predictive test negatives: findings from the EMBRACE study
F. Girardi, D. Barnes, D. Barrowdale, D. Frost +30 more
2018Genetics in Medicine18 citations Open access
Semantic Scholar
Epigenotype–genotype–phenotype correlations in SETD1A and SETD2 chromatin disorders
S. Lee, Lara Menzies, Eleanor M. Hay, Eguzkine Ochoa +19 more
2023Human Molecular Genetics17 citations Open access
Semantic Scholar
Incidence, puberty, and fertility in 45,X/47,XXX mosaicism: Report of a patient and a literature review
Richard Martin, Geoff Smith, J. Hughes, P. Morrison
2018American Journal of Medical Genetics. Part A17 citations
Semantic Scholar
Lymphocyte telomere length is long in BRCA1 and BRCA2 mutation carriers regardless of cancer-affected status
K. Pooley, L. McGuffog, D. Barrowdale, D. Frost +32 more
2014Cancer Epidemiology, Biomarkers and Prevention17 citations Open access
Semantic Scholar
Maximising survival: the main concern of women with hereditary breast and ovarian cancer who undergo genetic testing for BRCA1/2.
L. Jeffers, P. Morrison, E. McCaughan, D. Fitzsimons
2014European Journal of Oncology Nursing16 citations
Semantic Scholar
Cantú syndrome with coexisting familial pituitary adenoma
P. Marques, Rupert Spencer, P. Morrison, I. Carr +4 more
2018Endocrine15 citations Open access
Semantic Scholar
Characterization of renal cell carcinoma‐associated constitutional chromosome abnormalities by genome sequencing
Philip S. Smith, James Whitworth, Hannah D. West, J. Cook +9 more
2020Genes, Chromosomes and Cancer14 citations Open access
Semantic Scholar
Uptake of health monitoring and disease self‐management in Australian adults with neurofibromatosis type 1: strategies to improve care
H. Crawford, B. Barton, M. Wilson, Y. Berman +3 more
2016Clinical Genetics14 citations
Semantic Scholar
Genetic defects are common in myopathies with tubular aggregates
Q. Gang, C. Bettencourt, S. Brady, J. Holton +16 more
2021Annals of Clinical and Translational Neurology13 citations Open access
Semantic Scholar
The frequency of spinocerebellar ataxia type 23 in a UK population
K. Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, Sherif Hamed +11 more
2013Journal of Neurology13 citations
Semantic Scholar
SDHC phaeochromocytoma and paraganglioma: A UK‐wide case series
Sophie T. Williams, P. Chatzikyriakou, P. Carroll, B. McGowan +33 more
2021Clinical Endocrinology12 citations Open access
Semantic Scholar
Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral Palsy
Gillian Rea, S. Tirupathi, Jonathan Williams, P. Clouston +1 more
2019Cerebellum12 citations Open access
Semantic Scholar
Hereditary Gigantism-the biblical giant Goliath and his brothers
D. Donnelly, P. Morrison
2014Ulster medical journal12 citations
Semantic Scholar
Prostate Cancer Risk by BRCA2 Genomic Regions
T. Nyberg, D. Frost, D. Barrowdale, D. Evans +29 more
2020European Urology11 citations Open access
Semantic Scholar
Utility of genome sequencing and group-enrichment to support splice variant interpretation in Marfan syndrome
Susan Walker, D. Bunyan, H. Thomas, Yesim Kesim +43 more
2025medRxiv5 citations Open access
Semantic Scholar
Sebaceous Carcinoma Arising in Ovarian Teratoma: First Report Associated With Germline Mismatch Repair Gene Mutation.
Jacinta M. Murray, P. Mcilwaine, P. Morrison, W. McCluggage
2021International Journal of Gynecological Pathology5 citations
Semantic Scholar

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