Peter D. Turnpenny

11.0k total citations
109 papers, 4.0k citations indexed

About

Peter D. Turnpenny is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Peter D. Turnpenny has authored 109 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 43 papers in Molecular Biology and 26 papers in Surgery. Recurrent topics in Peter D. Turnpenny's work include Connective tissue disorders research (14 papers), Pediatric Hepatobiliary Diseases and Treatments (13 papers) and Genomics and Rare Diseases (12 papers). Peter D. Turnpenny is often cited by papers focused on Connective tissue disorders research (14 papers), Pediatric Hepatobiliary Diseases and Treatments (13 papers) and Genomics and Rare Diseases (12 papers). Peter D. Turnpenny collaborates with scholars based in United Kingdom, United States and Australia. Peter D. Turnpenny's co-authors include Sian Ellard, Kenro Kusumi, Sally L. Dunwoodie, Neil V. Whittock, Timothy H.J. Goodship, Judith A. Goodship, Paul Warwicker, Duncan B. Sparrow, Rosemary L. Donne and Yves Pirson and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Nature Reviews Genetics.

In The Last Decade

Peter D. Turnpenny

108 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter D. Turnpenny United Kingdom 35 1.7k 1.4k 892 503 486 109 4.0k
Mustafa Tekin United States 42 3.0k 1.7× 1.5k 1.0× 438 0.5× 669 1.3× 274 0.6× 219 5.5k
Philippe Duquesnoy France 37 2.1k 1.2× 1.3k 0.9× 393 0.4× 735 1.5× 237 0.5× 71 4.0k
Andrew Read United Kingdom 38 3.0k 1.8× 1.7k 1.2× 819 0.9× 379 0.8× 554 1.1× 124 6.1k
Marco Seri Italy 38 2.3k 1.3× 1.4k 1.0× 1.1k 1.2× 488 1.0× 202 0.4× 193 5.3k
Mordechai Shohat Israel 25 1.6k 1.0× 699 0.5× 470 0.5× 551 1.1× 270 0.6× 106 2.9k
John R.W. Yates United Kingdom 33 2.2k 1.3× 1.5k 1.0× 494 0.6× 427 0.8× 513 1.1× 82 5.4k
Reijo Norio Finland 36 1.1k 0.7× 1.8k 1.2× 337 0.4× 447 0.9× 401 0.8× 69 3.6k
Catherine Dodé France 36 2.8k 1.6× 1.3k 0.9× 304 0.3× 846 1.7× 189 0.4× 92 4.7k
Joël Zlotogora Israel 35 1.9k 1.1× 2.0k 1.4× 381 0.4× 234 0.5× 690 1.4× 170 5.0k
Gen Nishimura Japan 41 3.6k 2.1× 3.7k 2.6× 781 0.9× 384 0.8× 541 1.1× 344 7.1k

Countries citing papers authored by Peter D. Turnpenny

Since Specialization
Citations

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

Fields of papers citing papers by Peter D. Turnpenny

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter D. Turnpenny. 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 Peter D. Turnpenny. The network helps show where Peter D. Turnpenny may publish in the future.

Co-authorship network of co-authors of Peter D. Turnpenny

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

All Works

20 of 20 papers shown
1.
Clayton‐Smith, Jill, Penny A. Cook, Christopher M. Morris, et al.. (2023). Neurodevelopmental outcomes in children and adults with Fetal Valproate Spectrum Disorder: A contribution from the ConcePTION project. Neurotoxicology and Teratology. 100. 107292–107292. 6 indexed citations
2.
Kumar, Ajith, Angela F. Brady, Tessa Homfray, et al.. (2022). Expanding the phenotype of TAB2 variants and literature review. American Journal of Medical Genetics Part A. 188(11). 3331–3342. 6 indexed citations
3.
Hadden, Robert D. M., et al.. (2019). Amniotic band sequence in paternal half‐siblings with vascular Ehlers–Danlos syndrome. American Journal of Medical Genetics Part A. 182(3). 553–556. 5 indexed citations
4.
Piña-Aguilar, Raúl E., Sheila A Simpson, Angus Clarke, et al.. (2018). 27 years of prenatal diagnosis for Huntington disease in the United Kingdom. Genetics in Medicine. 21(7). 1639–1643. 9 indexed citations
5.
Giampietro, Philip F., Olivier Pourquié, Shiro Ikegawa, et al.. (2017). Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16–18, 2017, Dallas, Texas. American Journal of Medical Genetics Part A. 176(1). 253–256. 5 indexed citations
6.
Carrieri, Daniele, Anneke Lucassen, Angus Clarke, et al.. (2016). Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom. Genetics in Medicine. 18(9). 876–881. 40 indexed citations
7.
Campeau, Philippe M., Guy M. Lenk, Yangjin Bae, et al.. (2013). Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase. The American Journal of Human Genetics. 92(5). 781–791. 115 indexed citations
8.
Donnelly, Deirdre E., Peter D. Turnpenny, & Vivienne McConnell. (2011). Phenotypic variability in a three-generation Northern Irish family with Sotos syndrome. Clinical Dysmorphology. 20(4). 175–181. 5 indexed citations
9.
Gucev, Zoran, Velibor Tasić, Nada Pop‐Jordanova, et al.. (2010). Autosomal dominant spondylocostal dysostosis in three generations of a Macedonian family: Negative mutation analysis of DLL3, MESP2, HES7, and LFNG. American Journal of Medical Genetics Part A. 152A(6). 1378–1382. 18 indexed citations
10.
Turnpenny, Peter D.. (2008). Defective Somitogenesis and Abnormal Vertebral Segmentation in Man. Advances in experimental medicine and biology. 638. 164–189. 5 indexed citations
11.
Williams, Justin H. G., et al.. (2007). Characteristics of fetal anticonvulsant syndrome associated autistic disorder. Developmental Medicine & Child Neurology. 47(8). 551–555. 31 indexed citations
12.
Kusumi, Kenro & Peter D. Turnpenny. (2007). Formation Errors of the Vertebral Column. Journal of Bone and Joint Surgery. 89(suppl_1). 64–71. 21 indexed citations
13.
14.
Irving, Melita, Helen Hanson, Peter D. Turnpenny, et al.. (2003). Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases. American Journal of Medical Genetics Part A. 123A(2). 153–163. 53 indexed citations
15.
Turnpenny, Peter D., Michael Bulman, Timothy M. Frayling, et al.. (1999). A Gene for Autosomal Recessive Spondylocostal Dysostosis Maps to 19q13.1-q13.3. The American Journal of Human Genetics. 65(1). 175–182. 57 indexed citations
16.
Warwicker, Paul, Timothy H.J. Goodship, Rosemary L. Donne, et al.. (1998). Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney International. 53(4). 836–844. 373 indexed citations
17.
Turnpenny, Peter D., et al.. (1995). A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?. Clinical Dysmorphology. 4(4). 324–333. 5 indexed citations
18.
Turnpenny, Peter D. & Alastair F. Nimmo. (1993). Fractured clavicle of the newborn in a population with a high prevalence of grand‐multiparity: analysis of 78 consecutive cases. BJOG An International Journal of Obstetrics & Gynaecology. 100(4). 338–341. 26 indexed citations
19.
Turnpenny, Peter D., et al.. (1993). Adoption, genetic disease, and DNA.. Archives of Disease in Childhood. 69(4). 411–413. 4 indexed citations
20.
Turnpenny, Peter D., et al.. (1992). Recurrent miscarriage, cystic hygroma and incontinentia pigmenti. BJOG An International Journal of Obstetrics & Gynaecology. 99(11). 920–930. 2 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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