Rebecca C. Pollitt

2.5k citations

20 papers · 309 indexed · h-index 11

Genetics top 10%
- Connective tissue disorders research 18
- Dermatological and Skeletal Disorders 3
- Chronic Lymphocytic Leukemia Research 2
Rheumatology top 10%
- Bone and Dental Protein Studies 7
Genetics
- Connective tissue disorders research 18
- Dermatological and Skeletal Disorders 3
- Chronic Lymphocytic Leukemia Research 2
Cancer Research
Hematology
Oncology
- Bone health and treatments 3
Molecular Biology
- Ubiquitin and proteasome pathways 3
- Cancer-related gene regulation 3
Public Health, Environmental and Occupational Health
- Acute Lymphoblastic Leukemia research 2

Co-authors: Nicholas Bishop Ann Dalton Meena Balasubramanian Janice Nunn Robert McMahon Paul Arundel M. Zulf Mughal Amaka C Offiah
Cited by: Genetics Rheumatology Cancer Research
Journals: British Journal of Haematology (2 papers)Human Mutation (1 paper)Gene (1 paper)
Partner nations: United Kingdom Austria Denmark

In The Last Decade

Rebecca C. Pollitt

20 papers receiving 301 citations

Peers

Countries citing papers authored by Rebecca C. Pollitt

Since Specialization

Citations

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

Fields of papers citing papers by Rebecca C. Pollitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rebecca C. Pollitt. 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 Rebecca C. Pollitt. The network helps show where Rebecca C. Pollitt may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Absence of Collagen Flowers on Electron Microscopy and Identification of (Likely) Pathogenic COL5A1 Variants in Two Patients Genes ·Lyazzat Kulzhabayeva,Angela F. Brady,Marina Colombi,David Ferguson,Rebecca C. Pollitt,F. Michael Pope,Marco Ritelli,Sofie Symoens,Neeti Ghali,Fleur S. van Dijk	2019	11
2	Bilateral giant retinal tears in Osteogenesis Imperfecta BMC Medical Genetics ·Paolo Scollo,Martin P. Snead,Allan J. Richards,Rebecca C. Pollitt,Catherine DeVile	2018	11
3	Novel PLS3 variants in X‐linked osteoporosis: Exploring bone material properties American Journal of Medical Genetics Part A ·Meena Balasubramanian,Nadja Fratzl‐Zelman,Ming-Xing Yang,Suliman Kharashi,Nicola Peel,Rebecca C. Pollitt,А.В. Пищова,Elizabeth Milne,Kath Smith,Paul Roschger,Klaus Klaushofer,Nicholas Bishop	2018	23
4	A novel COL1A1 mutation causing a variant of osteogenesis imperfecta Clinical Dysmorphology ·Nesterenko Dk,Avril Mason,Rebecca C. Pollitt,S. Faisal Ahmed,Esther Kinning	2017	1
5	P4HB recurrent missense mutation causing Cole-Carpenter syndrome Journal of Medical Genetics ·Meena Balasubramanian,Raja Padidela,Rebecca C. Pollitt,Nicholas Bishop,M. Zulf Mughal,Amaka C Offiah,Bart Wagner,Janine McCaughey,David Stephens	2017	17
6	Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations American Journal of Medical Genetics Part A ·Rebecca C. Pollitt,Vrinda Saraff,Ann Dalton,Emma Webb,Nick J. Shaw,Glenda Sobey,M. Zulf Mughal,Emma Hobson,Тетяна Нескородєва,Nicholas Bishop,Paul Arundel,Wolfgang Högler,Meena Balasubramanian	2016	27
7	A novel homozygous variant in SERPINH1 associated with a severe, lethal presentation of osteogenesis imperfecta with hydranencephaly Gene ·Charlotte J. Marshall,G. Guipert,Orlando César Antunes Gonçalves,Rebecca C. Pollitt,Meena Balasubramanian	2016	15
8	Compound heterozygous variants in NBAS as a cause of atypical osteogenesis imperfecta Bone ·Meena Balasubramanian,Jane A. Hurst,Stephen Brown,Nick Bishop,Paul Arundel,Catherine DeVile,Rebecca C. Pollitt,Lucy Crooks,Dáša Longman,Javier F. Cáceres,Fiona Shackley,Sally Connolly,Jeanette H. Payne,Amaka C Offiah,David J. Hughes,Michael Parker,(unknown),Timothy M. Skerry	2016	37
9	Diagnostic conundrums in antenatal presentation of a skeletal dysplasia with description of a heterozygous C‐propeptide mutation in COL1A1 associated with a severe presentation of osteogenesis imperfecta American Journal of Medical Genetics Part A ·Charlotte J. Marshall,Paul Arundel,Talat Mushtaq,Amaka C Offiah,Rebecca C. Pollitt,Nicholas Bishop,Meena Balasubramanian	2016	3
10	Clinical, structural, biochemical and X‐ray crystallographic correlates of pathogenicity for variants in the C‐propeptide region of the COL3A1 gene American Journal of Medical Genetics Part A ·Laurence Hauptman,Anthony M. Vandersteen,Neeti Ghali,Philip Sawle,Stephanie Wachs,Rebecca C. Pollitt,David Ferguson,Simon Holden,Frances Elmslie,Alex Henderson,David Hulmes,F M Pope	2015	7
11	CRTAPmutation in a patient with Cole‐Carpenter syndrome American Journal of Medical Genetics Part A ·Meena Balasubramanian,Rebecca C. Pollitt,Kate Chandler,M. Zulf Mughal,Michael Parker,Ann Dalton,Paul Arundel,Amaka C Offiah,Nicholas Bishop	2015	19
12	A combined vascular surgical and clinical genetics approach to diffuse aneurysmal disease Annals of The Royal College of Surgeons of England ·Kyle D. Lewis,Andrew M.T.L. Choong,Natalie Canham,Sophie Renton,Rebecca C. Pollitt,Stephanie Wachs,BRETT R. HORWITZ,Lily Islam,K.E. Guerman,Neeti Ghali,Anthony Vandersteen	2015	3
13	Palmoplantar contractures in childhood: a rare complication of vascular Ehlers-Danlos syndrome Clinical and Experimental Dermatology ·Amy Foulkes,Rebecca C. Pollitt,Glenda Sobey,Roberto Sánchez Medina,Aileen Taylor	2013	2
14	Four patients with Sillence type I osteogenesis imperfecta and mild bone fragility, complicated by left ventricular cardiac valvular disease and cardiac tissue fragility caused by type I collagen mutations American Journal of Medical Genetics Part A ·Anthony M. Vandersteen,Allan M. Lund,David Ferguson,Philip Sawle,Rebecca C. Pollitt,Susan Holder,Emma Wakeling,Neil Moat,F. Michael Pope	2013	12
15	Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta Endocrinology Diabetes and Metabolism Case Reports ·宮本啓二,EA Vessel,Nicholas Owen,Rebecca C. Pollitt,Alison L. Harte,Philip G. McTernan,Gyanendra Tripathi,Thomas M. Barber	2013	2
16	Femoral Artery Dissection in Vascular Type Ehlers–Danlos Syndrome; Leave Well Alone? European Journal of Vascular and Endovascular Surgery ·Michael Singh,Sapna Puppala,Rebecca C. Pollitt,Glenda Sobey,D J A Scott	2012	6
17	Type 1 collagenopathy presenting with a Russell–Silver phenotype American Journal of Medical Genetics Part A ·Michael Parker,유선나,Julia Rankin,Louise C. Wilson,Meena Balasubramanian,Christine M Hall,Bart Wagner,Rebecca C. Pollitt,Ann Dalton,Nicholas Bishop	2011	6
18	Mutation analysis ofCOL1A1andCOL1A2in patients diagnosed with osteogenesis imperfecta type I-IV Human Mutation ·Rebecca C. Pollitt,Robert McMahon,Janice Nunn,Jiaru Zeng,Y. Vargas-Luna,Nicholas Bishop,Ann Dalton	2006	77
19	Are aberrant BCR-ABL transcripts more common than previously thought? British Journal of Haematology ·G. A. Wilson,Elisabeth Vandenberghe,Rebecca C. Pollitt,David C. Rees,Anne Goodeve,I. R. Peake,John T. Reilly	2000	28
20	Are aberrant BCR–ABL transcripts more common than previously thought? British Journal of Haematology ·G. A. Wilson,Elisabeth Vandenberghe,Rebecca C. Pollitt,Douglas C. Rees,Anne Goodeve,I. R. Peake,John T. Reilly	2000	2

About Rebecca C. Pollitt

Rebecca C. Pollitt is a scholar working on Genetics, Rheumatology, Hematology, Genetics and Immunology and Allergy, having authored 20 papers that have together received 309 indexed citations. Recurring topics across this work include Connective tissue disorders research (18 papers), Bone and Dental Protein Studies (7 papers), Dermatological and Skeletal Disorders (3 papers), Bone health and treatments (3 papers), Ubiquitin and proteasome pathways (3 papers), Cancer-related gene regulation (3 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). The work is most often cited by research in Genetics (216 citations), Rheumatology (110 citations), Genetics (39 citations), Cancer Research (49 citations) and Hematology (34 citations). Rebecca C. Pollitt has collaborated with scholars based in United Kingdom, Austria and Denmark. Frequent co-authors include Nicholas Bishop, Ann Dalton, Meena Balasubramanian, Janice Nunn, Robert McMahon, Paul Arundel, M. Zulf Mughal, Amaka C Offiah, Michael Parker and John T. Reilly. Their work appears in journals such as British Journal of Haematology, Human Mutation, Gene, Clinical and Experimental Dermatology and Journal of Medical Genetics.

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