P. Renwick

665 total citations
14 papers, 464 citations indexed

About

P. Renwick is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Infectious Diseases. According to data from OpenAlex, P. Renwick has authored 14 papers receiving a total of 464 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Infectious Diseases. Recurrent topics in P. Renwick's work include Prenatal Screening and Diagnostics (4 papers), RNA modifications and cancer (2 papers) and Skin and Cellular Biology Research (2 papers). P. Renwick is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), RNA modifications and cancer (2 papers) and Skin and Cellular Biology Research (2 papers). P. Renwick collaborates with scholars based in United Kingdom, United States and Belgium. P. Renwick's co-authors include Paola Dal Cin, Christopher D.�M. Fletcher, Herman Van den Berghe, Céline Moutou, Joanne Traeger‐Synodinos, Edith Coonen, V. Goossens, Kamila Veselá, Martine De Rycke and S. SenGupta and has published in prestigious journals such as Nucleic Acids Research, Journal of Investigative Dermatology and Gene.

In The Last Decade

P. Renwick

14 papers receiving 441 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
P. Renwick United Kingdom	7	189	178	105	79	79	14	464
Jacqueline R. Batanian United States	15	92 0.5×	76 0.4×	206 2.0×	52 0.7×	186 2.4×	56	568
F. M. Fink Austria	11	103 0.5×	46 0.3×	125 1.2×	32 0.4×	41 0.5×	21	439
Jeffrey M. Cloutier United States	14	138 0.7×	40 0.2×	538 5.1×	96 1.2×	150 1.9×	46	798
Marga Schepens Netherlands	14	120 0.6×	185 1.0×	539 5.1×	30 0.4×	336 4.3×	20	779
Shari Baldinger United States	11	143 0.8×	95 0.5×	244 2.3×	19 0.2×	266 3.4×	16	642
Paola De Sanctis Italy	14	65 0.3×	120 0.7×	239 2.3×	11 0.1×	21 0.3×	22	589
Susanne Zahn Germany	12	70 0.4×	24 0.1×	215 2.0×	19 0.2×	82 1.0×	14	402
Mitzi L. Murray United States	10	55 0.3×	29 0.2×	130 1.2×	51 0.6×	314 4.0×	13	467
Ulrike Gamerdinger Germany	11	74 0.4×	44 0.2×	190 1.8×	25 0.3×	105 1.3×	20	398
Fengchang Qiao China	18	65 0.3×	210 1.2×	697 6.6×	23 0.3×	165 2.1×	51	995

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-authorship network of co-authors of P. Renwick

This figure shows the co-authorship network connecting the top 25 collaborators of P. Renwick. A scholar is included among the top collaborators of P. Renwick 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 P. Renwick. P. Renwick is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Renwick, P., et al.. (2019). 1. EVALUATION AND IMPLEMENTATION OF ONEPGT FOR MONOGENIC CONDITIONS. Reproductive BioMedicine Online. 39. e26–e27. 1 indexed citations

Moutou, Céline, V. Goossens, Edith Coonen, et al.. (2014). ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010. Human Reproduction. 29(5). 880–903. 62 indexed citations

Fassihi, Hiva, et al.. (2010). Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa. British Journal of Dermatology. 162(6). 1330–1336. 13 indexed citations

Harper, J, Edith Coonen, Martine De Rycke, et al.. (2010). What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee . Human Reproduction. 25(4). 821–823. 127 indexed citations

Smith, Bradley, Steve Bevan, Caroline Vance, et al.. (2009). 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. 75(5). 485–489. 18 indexed citations

Fassihi, Hiva, P. Renwick, Cheryl Black, et al.. (2006). Development and application of preimplantation genetic diagnosis for inherited skin disorders in the UK. Journal of Investigative Dermatology. 126. 35–35. 1 indexed citations

Fassihi, Hiva, P. Renwick, Cheryl Black, & John A. McGrath. (2006). 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. 42(3). 241–248. 11 indexed citations

Renwick, P., A. J. Birley, & M.A. Hultén. (1997). Study of Alu sequences at the hypoxanthine phosphoribosyltransferase (hprt) encoding region of man. Gene. 184(2). 155–162. 4 indexed citations

Renwick, P., et al.. (1995). Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch‐Nyhan syndrome. Clinical Genetics. 48(2). 80–84. 6 indexed citations

10.

Renwick, P., B.R. Reeves, Paola Dal Cin, et al.. (1995). 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. 70(1-2). 58–63. 53 indexed citations

11.

Renwick, P., et al.. (1995). Physical linkage of the cdc2-related gene (PCTK1) and the ubiquitin-activating enzyme E1 gene (UBE1) on human Xp11.3. Cytogenetic and Genome Research. 71(2). 155–157. 5 indexed citations

12.

Renwick, P., et al.. (1995). Translocation t(12;16)(q13;p11) in myxoid liposarcoma and round cell liposarcoma: molecular and cytogenetic analysis.. PubMed. 55(1). 24–7. 156 indexed citations

13.

Renwick, P., et al.. (1992). AHinfI polymorphism in the human elastin gene (ELN). Nucleic Acids Research. 20(5). 1168–1168. 6 indexed citations

14.

Renwick, P., et al.. (1991). A Taql RFLP in the region of the HPRT locus. Nucleic Acids Research. 19(16). 4576–4576. 1 indexed citations

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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