W. J. Craigen

1.6k total citations
17 papers, 782 citations indexed

About

W. J. Craigen is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, W. J. Craigen has authored 17 papers receiving a total of 782 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 6 papers in Genetics. Recurrent topics in W. J. Craigen's work include Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (8 papers) and RNA modifications and cancer (3 papers). W. J. Craigen is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (8 papers) and RNA modifications and cancer (3 papers). W. J. Craigen collaborates with scholars based in United States, Canada and Italy. W. J. Craigen's co-authors include C. Thomas Caskey, C. Thomas Caskey, Gábor Veres, Wei Zhang, Margherita Milone, Jing Wang, Ni‐Chung Lee, Sha Tang, L. Wong and A.H.M. Mahbubul Huq and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Annals of Neurology.

In The Last Decade

W. J. Craigen

17 papers receiving 769 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
W. J. Craigen	635	304	160	79	59	17	782
Anne Douar	577 0.9×	110 0.4×	403 2.5×	28 0.4×	38 0.6×	20	807
Karen L. Yager	351 0.6×	53 0.2×	117 0.7×	30 0.4×	48 0.8×	8	493
Hayase Shisa	454 0.7×	53 0.2×	108 0.7×	18 0.2×	86 1.5×	52	678
Michaela Smolle	1.1k 1.7×	38 0.1×	85 0.5×	49 0.6×	31 0.5×	20	1.2k
Chika Sakai	324 0.5×	115 0.4×	35 0.2×	13 0.2×	141 2.4×	19	638
Chin-To Fong	198 0.3×	84 0.3×	95 0.6×	11 0.1×	85 1.4×	9	450
Lionel Grossbard	394 0.6×	57 0.2×	36 0.2×	69 0.9×	61 1.0×	9	728
Amelie S. Lotz‐Havla	207 0.3×	98 0.3×	33 0.2×	19 0.2×	86 1.5×	25	396
Takasumi Matsuki	314 0.5×	46 0.2×	59 0.4×	10 0.1×	223 3.8×	23	670
Thomas J. Nicholls	1.0k 1.6×	333 1.1×	64 0.4×	4 0.1×	57 1.0×	23	1.1k

Countries citing papers authored by W. J. Craigen

Since Specialization

Citations

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

Fields of papers citing papers by W. J. Craigen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W. J. Craigen

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

All Works

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17 of 17 papers shown

Dai, Hongzheng, Ayman W. El‐Hattab, Marwan Shinawi, et al.. (2016). FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome. Clinical Genetics. 91(4). 634–639. 19 indexed citations

Dharmadhikari, Avinash V., Przemysław Szafrański, Richard Person, et al.. (2012). Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148. Human Molecular Genetics. 21(15). 3345–3355. 17 indexed citations

Tang, Sha, Jing Wang, Ni‐Chung Lee, et al.. (2011). Mitochondrial DNA polymerase γ mutations: an ever expanding molecular and clinical spectrum. Journal of Medical Genetics. 48(10). 669–681. 125 indexed citations

Ware, Stephanie M., Nahed O. ElHassan, Stephen G. Kahler, et al.. (2009). Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes. Journal of Medical Genetics. 46(5). 308–314. 70 indexed citations

Dimmock, David, Carlo Dionisi‐Vici, Rosalba Carrozzo, et al.. (2008). Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase. Human Mutation. 29(2). 330–331. 123 indexed citations

Maheshwari, M., John W. Belmont, Rth Ho, et al.. (2002). PTPN11 Mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13. Human Mutation. 20(4). 298–304. 59 indexed citations

Craigen, W. J., et al.. (2000). Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII. Human Genetics. 106(1). 19–28. 23 indexed citations

Knaap, Marjo S. van der, C. Jakobs, Georg F. Hoffmann, et al.. (1999). D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity?. Annals of Neurology. 45(1). 111–119. 59 indexed citations

Huq, A.H.M. Mahbubul, Rhonda S. Lovell, C N Ou, Arthur L. Beaudet, & W. J. Craigen. (1997). X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death. Human Molecular Genetics. 6(11). 1803–1809. 58 indexed citations

10.

Craigen, W. J.. (1996). Persistent glycolic aciduria in a healthy child with normal alanine‐glyoxylate aminotransferase activity. Journal of Inherited Metabolic Disease. 19(6). 793–794. 6 indexed citations

11.

Craigen, W. J., Rhonda S. Lovell, & Margaret J. Sampson. (1994). Structure and expression of mouse mitochondrial voltage dependent anion channel genes. The American Journal of Human Genetics. 55. 2 indexed citations

12.

Anderson, Kent L., et al.. (1994). De novo proximal interstitial deletions of 14q: Cytogenetic and molecular investigations. American Journal of Medical Genetics. 52(1). 44–50. 27 indexed citations

13.

Craigen, W. J., et al.. (1990). Recent advances in peptide chain termination. Molecular Microbiology. 4(6). 861–865. 60 indexed citations

14.

Craigen, W. J., et al.. (1990). Cloning and expression of a mammalian peptide chain release factor with sequence similarity to tryptophanyl-tRNA synthetases.. Proceedings of the National Academy of Sciences. 87(9). 3508–3512. 44 indexed citations

15.

Jones, Stephen N., et al.. (1990). Ectopic correction of ornithine transcarbamylase deficiency in sparse fur mice.. Journal of Biological Chemistry. 265(24). 14684–14690. 42 indexed citations

16.

Kohara, Yuji, et al.. (1988). Rapid and precise mapping of the Escherichia coli release factor genes by two physical approaches. Journal of Bacteriology. 170(10). 4537–4541. 23 indexed citations

17.

Veres, Gábor, W. J. Craigen, & C. Thomas Caskey. (1986). The 5' flanking region of the ornithine transcarbamylase gene contains DNA sequences regulating tissue-specific expression.. Journal of Biological Chemistry. 261(17). 7588–7591. 25 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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