William Craigen

1.0k total citations
13 papers, 443 citations indexed

About

William Craigen is a scholar working on Molecular Biology, Clinical Biochemistry and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, William Craigen has authored 13 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 3 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in William Craigen's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). William Craigen is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). William Craigen collaborates with scholars based in United States, Australia and China. William Craigen's co-authors include Victoria L. Harvey, Michelangelo Campanella, Jemma Gatliff, Peter J. Parker, Rosella Abeti, Daniel A. East, F. H. Bronson, Gail E. Herman, C. Jakobs and K. Michael Gibson and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

William Craigen

12 papers receiving 434 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William Craigen United States 9 290 114 81 53 52 13 443
M. Pineda Spain 13 285 1.0× 127 1.1× 118 1.5× 67 1.3× 48 0.9× 26 533
Alfonso Oyarzábal Spain 11 242 0.8× 156 1.4× 79 1.0× 72 1.4× 19 0.4× 18 452
Marjan E. Steenweg Netherlands 11 509 1.8× 160 1.4× 31 0.4× 88 1.7× 40 0.8× 16 621
Helene Bruhn Sweden 11 346 1.2× 127 1.1× 60 0.7× 19 0.4× 35 0.7× 19 433
Anthony S. Castanza United States 5 410 1.4× 121 1.1× 46 0.6× 111 2.1× 56 1.1× 5 534
Charlotte Thiels Germany 11 225 0.8× 40 0.4× 46 0.6× 66 1.2× 32 0.6× 25 399
I Klisak United States 13 405 1.4× 53 0.5× 124 1.5× 80 1.5× 21 0.4× 19 682
Simon Heales United Kingdom 7 274 0.9× 92 0.8× 23 0.3× 84 1.6× 98 1.9× 12 536
M. Barth France 12 217 0.7× 46 0.4× 140 1.7× 128 2.4× 58 1.1× 17 423
Anaïs Thouin United Kingdom 6 108 0.4× 52 0.5× 49 0.6× 70 1.3× 21 0.4× 7 281

Countries citing papers authored by William Craigen

Since Specialization
Citations

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

Fields of papers citing papers by William Craigen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William Craigen

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

All Works

13 of 13 papers shown
1.
Zhao, Sen, Shenglan Li, Jill A. Rosenfeld, et al.. (2025). The utility of ultra-deep RNA sequencing in Mendelian disorder diagnostics. The American Journal of Human Genetics. 112(11). 2578–2590.
2.
Caldovic, Ljubica, William Craigen, Annette Feigenbaum, et al.. (2023). CURATION OF SEQUENCE VARIANTS IN UREA CYCLE GENES. Molecular Genetics and Metabolism. 138(3). 107488–107488. 1 indexed citations
3.
Tremblay, Martine, Andrew Aldridge, Jill A. Rosenfeld, et al.. (2021). Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4. Human Molecular Genetics. 31(9). 1430–1442. 8 indexed citations
4.
Pillai, Nishitha R., Bridget M. Stroup, Brian J. Shayota, et al.. (2019). Liver transplantation in propionic and methylmalonic acidemia: A single center study with literature review. Molecular Genetics and Metabolism. 128(4). 431–443. 43 indexed citations
5.
Lauterwasser, Joachim, Franziska Todt, Ralf M. Zerbes, et al.. (2016). The porin VDAC2 is the mitochondrial platform for Bax retrotranslocation. Scientific Reports. 6(1). 32994–32994. 66 indexed citations
6.
Gatliff, Jemma, Daniel A. East, Rosella Abeti, et al.. (2014). TSPO interacts with VDAC1 and triggers a ROS-mediated inhibition of mitochondrial quality control. Autophagy. 10(12). 2279–2296. 165 indexed citations
7.
Szafrański, Przemysław, Sailaja Golla, Weihong Jin, et al.. (2014). Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications. European Journal of Human Genetics. 23(7). 915–921. 32 indexed citations
8.
El‐Hattab, Ayman W., Fangyuan Li, Eric Schmitt, et al.. (2010). 78 MPV17—Associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations. Mitochondrion. 10(2). 222–222. 7 indexed citations
9.
Brunetti‐Pierri, Nicola, Ayelet Erez, Oleg A. Shchelochkov, William Craigen, & Brendan Lee. (2009). Systemic hypertension in two patients with ASL deficiency: A result of nitric oxide deficiency?. Molecular Genetics and Metabolism. 98(1-2). 195–197. 26 indexed citations
10.
Erez, Ayelet, Xueqing Wang, Zhilian Xia, et al.. (2009). Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder. Neurogenetics. 10(4). 363–369. 32 indexed citations
11.
Jones, Derek K., et al.. (1995). Coal-black hyperpigmentation at birth in a child with congenital adrenal hypoplasia. Journal of the American Academy of Dermatology. 33(2). 323–326. 9 indexed citations
12.
Gibson, K. Michael, William Craigen, Gail E. Herman, & C. Jakobs. (1993). d‐2‐Hydroxyglutaric aciduria in a newborn with neurological abnormalities: A new neurometabolic disorder?. Journal of Inherited Metabolic Disease. 16(3). 497–500. 36 indexed citations
13.
Craigen, William & F. H. Bronson. (1982). Deterioration of the Capacity for Sexual Arousal in Aged Male Mice1. Biology of Reproduction. 26(5). 869–874. 18 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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