P. Renwick

665 citations

14 papers · 464 indexed · h-index 7

Impact in

Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
Pulmonary and Respiratory Medicine
- Sarcoma Diagnosis and Treatment

Papers in ⓘ

Molecular Biology 5
- Biochemical and Molecular Research 2
- RNA modifications and cancer 2
Pediatrics, Perinatology and Child Health 5
- Prenatal Screening and Diagnostics 4

Co-authors: Paola Dal Cin (2 shared papers)Christopher D.�M. Fletcher (2 shared papers)Herman Van den Berghe (1 shared paper)V. Goossens (2 shared papers)Joanne Traeger‐Synodinos (2 shared papers)Martine De Rycke (2 shared papers)Kamila Veselá (2 shared papers)Céline Moutou (2 shared papers)
Journals: Clinical Genetics (2 papers)Nucleic Acids Research (2 papers)Cytogenetic and Genome Research (2 papers)Human Reproduction (2 papers)Gene (1 paper)
Partner nations: United Kingdom United States Belgium

In The Last Decade

P. Renwick

14 papers receiving 441 citations

Peers

Countries citing papers authored by P. Renwick

Since Specialization

Citations

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

Fields of papers citing papers by P. Renwick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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14 of 14 papers shown

#	Work
1	Translocation t(12;16)(q13;p11) in myxoid liposarcoma and round cell liposarcoma: molecular and cytogenetic analysis. PubMed ·JC Knight, P. Renwick, Paola Dal Cin, Herman Van den Berghe, Christopher D.�M. Fletcher	1995	156
2	What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee Human Reproduction ·J Harper, Edith Coonen, Martine De Rycke, Francesco Fiorentino, Joep Geraedts, V. Goossens, G. Harton, Céline Moutou, T. Pehlivan Budak, P. Renwick, S. SenGupta, Joanne Traeger‐Synodinos, Kamila Veselá	2010	127
3	ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010 Human Reproduction ·Céline Moutou, V. Goossens, Edith Coonen, Martine De Rycke, Georgia Kokkali, P. Renwick, Sioban SenGupta, Kamila Veselá, Joanne Traeger‐Synodinos	2014	62
4	Two categories of synovial sarcoma defined by divergent chromosome translocation breakpoints in Xp11.2, with implications for the histologic sub-classification of synovial sarcoma Cytogenetic and Genome Research ·P. Renwick, B.R. Reeves, Paola Dal Cin, Christopher D.�M. Fletcher, Helena Kempski, Raf Sciot, Bernd Kazmierczak, K. Jani, H Sonobe, J.C. Knight	1995	53
5	Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra‐familial variability in age of onset and complex phenotype Clinical Genetics ·Bradley Smith, Steve Bevan, Caroline Vance, P. Renwick, Philip A. Wilkinson, Christos Proukakis, Ferdinando Squitieri, Alfredo Berardelli, Thomas T. Warner, Evan Reid, Christopher E. Shaw	2009	18
6	Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa British Journal of Dermatology ·Hiva Fassihi, Lanhui Liu, P. Renwick, PR Braude, John A. McGrath	2010	13
7	Single cell PCR amplification of microsatellites flanking the COL7A1 gene and suitability for preimplantation genetic diagnosis of Hallopeau–Siemens recessive dystrophic epidermolysis bullosa Journal of Dermatological Science ·Hiva Fassihi, P. Renwick, Cheryl Black, John A. McGrath	2006	11
8	Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch‐Nyhan syndrome Clinical Genetics ·P. Renwick, A. J. Birley, Carole M. E. McKeown, M.A. Hultén	1995	6
9	AHinfI polymorphism in the human elastin gene (ELN) Nucleic Acids Research ·M. C. Raybould, P. Renwick, A. Biriey, M. Hulteén	1992	6
10	Physical linkage of the cdc2-related gene (PCTK1) and the ubiquitin-activating enzyme E1 gene (UBE1) on human Xp11.3 Cytogenetic and Genome Research ·J.C. Knight, P. Renwick, James R. Downing, Tsukasa Okuda	1995	5
11	Study of Alu sequences at the hypoxanthine phosphoribosyltransferase (hprt) encoding region of man Gene ·P. Renwick, A. J. Birley, M.A. Hultén	1997	4
12	Development and application of preimplantation genetic diagnosis for inherited skin disorders in the UK Journal of Investigative Dermatology ·Hiva Fassihi, P. Renwick, Cheryl Black, Susan J. Pickering, Peter Braude, John A. McGrath	2006	1
13	A Taql RFLP in the region of the HPRT locus Nucleic Acids Research ·P. Renwick, M. C. Raybould, A. J. Birley, M. Hullén	1991	1
14	1. EVALUATION AND IMPLEMENTATION OF ONEPGT FOR MONOGENIC CONDITIONS Reproductive BioMedicine Online ·P. Renwick, Josefa González, Heema Hewitson	2019	1

About P. Renwick

P. Renwick is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Infectious Diseases, Genetics and Pathology and Forensic Medicine, having authored 14 papers that have together received 464 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Biochemical and Molecular Research (2 papers), Parvovirus B19 Infection Studies (2 papers), Skin and Cellular Biology Research (2 papers), RNA modifications and cancer (2 papers), Cardiac tumors and thrombi (2 papers), Genetic and rare skin diseases. (2 papers) and Sarcoma Diagnosis and Treatment (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (178 citations), Pulmonary and Respiratory Medicine (189 citations), Rheumatology (79 citations), Reproductive Medicine (43 citations) and Pathology and Forensic Medicine (61 citations). P. Renwick has collaborated with scholars based in United Kingdom, United States and Belgium. Frequent co-authors include Paola Dal Cin, Christopher D.�M. Fletcher, Herman Van den Berghe, V. Goossens, Joanne Traeger‐Synodinos, Martine De Rycke, Kamila Veselá, Céline Moutou, Edith Coonen and Francesco Fiorentino. Their work appears in journals such as Clinical Genetics, Nucleic Acids Research, Cytogenetic and Genome Research, Human Reproduction and Gene.

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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