Germaine Pierre

687 total citations
16 papers, 187 citations indexed

About

Germaine Pierre is a scholar working on Clinical Biochemistry, Molecular Biology and Surgery. According to data from OpenAlex, Germaine Pierre has authored 16 papers receiving a total of 187 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Biochemistry, 7 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Germaine Pierre's work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (4 papers) and Pediatric Hepatobiliary Diseases and Treatments (3 papers). Germaine Pierre is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (4 papers) and Pediatric Hepatobiliary Diseases and Treatments (3 papers). Germaine Pierre collaborates with scholars based in United Kingdom, United States and Netherlands. Germaine Pierre's co-authors include Patrick McKiernan, Anupam Chakrapani, Kenneth D.R. Setchell, Mary Anne Preece, Carolyn L. Taylor, Hilary J. Vernon, Sarah Lawson, Geothy Chakupurakal, Christian J. Hendriksz and César H. Casale and has published in prestigious journals such as The Journal of Pediatrics, Archives of Disease in Childhood and European Journal of Human Genetics.

In The Last Decade

Germaine Pierre

13 papers receiving 181 citations

Peers

Germaine Pierre

SURGE

GENET

ONCOL

Said Al‐Yahyaee Oman

Mahshid S. Azamian United States

Sirisak Chanprasert United States

Helen Jiang United States

Christina Willenborg Germany

Kate Craig United Kingdom

Esmeralda Rodrigues Portugal

Michelina Sibilio Italy

Naomi Meeks United States

Anne Dieux‐Coëslier France

Said Al‐Yahyaee Oman

Germaine Pierre

84 ×0.8

32 ×0.6

56 ×1.4

SURGE

64 ×1.7

GENET

14 ×0.6

ONCOL

Citations per year, relative to Germaine Pierre Germaine Pierre (= 1×) peers Said Al‐Yahyaee

Countries citing papers authored by Germaine Pierre

Since Specialization

Citations

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

Fields of papers citing papers by Germaine Pierre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Germaine Pierre

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

All Works

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16 of 16 papers shown

Carling, Rachel S., Anupam Chakrapani, Patricia Hall, et al.. (2024). Retrospective Review of Positive Newborn Screening Results for Isovaleric Acidemia and Development of a Strategy to Improve the Efficacy of Newborn Screening in the UK. International Journal of Neonatal Screening. 10(1). 24–24.

Pierre, Germaine, et al.. (2023). Left ventricular noncompaction cardiomyopathy and short QT syndrome due to primary carnitine deficiency. Annals of Noninvasive Electrocardiology. 28(6). e13077–e13077. 1 indexed citations

Pierre, Germaine, et al.. (2023). Think hyperammonaemia: the importance of early clinical management in urea cycle disorders. Paediatrics and Child Health. 33(3). 57–64. 1 indexed citations

Pierre, Germaine, Peta Sharples, Seth Love, et al.. (2022). Severe Congenital Myopathy and Neuropathy with Congenital Cataracts due to GFER Variant: A Neuropathological Study. Journal of Pediatric Neurology. 22(1). 50–55.

Gripp, Karen W., Sarah Smithson, Ingrid Scurr, et al.. (2021). Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies. European Journal of Human Genetics. 29(9). 1384–1395. 25 indexed citations

Taylor, Carolyn L., et al.. (2021). Clinical presentation and natural history of Barth Syndrome: An overview. Journal of Inherited Metabolic Disease. 45(1). 7–16. 39 indexed citations

Alston, Charlotte L., Júlia Filardi Paim, Yi Shiau Ng, et al.. (2020). Early‐onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic COQ8A variants, including a large intragenic deletion. JIMD Reports. 54(1). 45–53. 8 indexed citations

Pierre, Germaine, Simon C Langton Hewer, Kayal Vijayakumar, et al.. (2019). A novel de novo ACTA1 variant in a patient with nemaline myopathy and mitochondrial Complex I deficiency. Neuromuscular Disorders. 30(2). 159–164. 7 indexed citations

Vara, Roshni, Anil Dhawan, Maesha Deheragoda, et al.. (2018). Liver transplantation for neonatal‐onset citrullinemia. Pediatric Transplantation. 22(4). e13191–e13191. 9 indexed citations

10.

Pierre, Germaine, et al.. (2018). P37 A single paediatric centre experience of l-carnitine supplementation in medium-chain acyl-coa dehydrogenase deficiency (mcadd). Archives of Disease in Childhood. 103(2). e2.41–e2.

11.

Broomfield, Alexander, Jean Mercer, Heather J. Church, et al.. (2017). Combined therapeutic approach to protein losing enteropathy complicating type 3 Gaucher disease using eliglustat. Molecular Genetics and Metabolism. 120(1-2). S32–S32. 1 indexed citations

12.

Pierre, Germaine, et al.. (2017). Metabolic disorders presenting as liver disease. Paediatrics and Child Health. 27(12). 533–539. 6 indexed citations

13.

Menao, Sebastián, María Arnedo, Beatriz Puisac, et al.. (2013). New case of mitochondrial HMG-CoA synthase deficiency. Functional analysis of eight mutations. European Journal of Medical Genetics. 56(8). 411–415. 24 indexed citations

14.

Pierre, Germaine, et al.. (2013). Metabolic disorders presenting as liver disease. Paediatrics and Child Health. 23(12). 509–515. 4 indexed citations

15.

Pierre, Germaine, Geothy Chakupurakal, Patrick McKiernan, et al.. (2008). Bone Marrow Transplantation in Glycogen Storage Disease Type 1b. The Journal of Pediatrics. 152(2). 286–288. 21 indexed citations

16.

Pierre, Germaine, et al.. (2008). Prospective treatment of cerebrotendinous xanthomatosis with cholic acid therapy. Journal of Inherited Metabolic Disease. 31(S2). 241–245. 41 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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