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 United Kingdom. W. J. Craigen's co-authors include C. Thomas Caskey, C. Thomas Caskey, Gábor Veres, Margherita Milone, Wei Zhang, Ni‐Chung Lee, Sha Tang, Jing Wang, 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

Peers

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

#	Work	Indexed citations
1	FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome 2016 ·Clinical Genetics ·Hongzheng Dai, (unknown), Ayman W. El‐Hattab, (unknown), Marwan Shinawi, Matthew A. Lines, Andreas Schulze, Michael A. McNutt, Garrett Gotway, Xiaoyan Tian, (unknown), Jia‐Yi Wang, W. J. Craigen, (unknown)	19
2	Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148 2012 ·Human Molecular Genetics ·Avinash V. Dharmadhikari, (unknown), Przemysław Szafrański, Richard Person, Smita Sampath, Siddharth K. Prakash, Patricia I. Bader, John A. Phillips, Vickie Hannig, Melissa Williams, Sherry Vinson, Angus A. Wilfong, Tyler Reimschisel, W. J. Craigen, Ankita Patel, Weimin Bi, J.R. Lupski, John W. Belmont, Sau Wai Cheung, Paweł Stankiewicz	17
3	Mitochondrial DNA polymerase γ mutations: an ever expanding molecular and clinical spectrum 2011 ·Journal of Medical Genetics ·Sha Tang, Jing Wang, Ni‐Chung Lee, Margherita Milone, (unknown), (unknown), W. J. Craigen, Wei Zhang, L. Wong	125
4	Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes 2009 ·Journal of Medical Genetics ·Stephanie M. Ware, Nahed O. ElHassan, Stephen G. Kahler, (unknown), (unknown), Erin Miller, Brenda Wong, R. Spicer, W. J. Craigen, Beth A. Kozel, Dorothy K. Grange, (unknown)	70
5	Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase 2008 ·Human Mutation ·David Dimmock, (unknown), Carlo Dionisi‐Vici, Rosalba Carrozzo, Joseph T.C. Shieh, (unknown), Cavatina K. Truong, Eric Schmitt, (unknown), S. Lucioli, Filippo M. Santorelli, (unknown), (unknown), Klaas J. Wierenga, Gregory M. Enns, Nicola Longo, Mark Lipson, Hilary Vallance, W. J. Craigen, Fernando Scaglia, (unknown)	123
6	PTPN11 Mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13 2002 ·Human Mutation ·M. Maheshwari, John W. Belmont, (unknown), Rth Ho, Luciano Molinari, (unknown), (unknown), (unknown), Jeffery A. Towbin, W. J. Craigen, J. Raphael Gibbs	59
7	Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII 2000 ·Human Genetics ·(unknown), W. J. Craigen, Lynne T. Smith, Douglas R. Keene, Peter H. Byers	23
8	D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity? 1999 ·Annals of Neurology ·Marjo S. van der Knaap, C. Jakobs, Georg F. Hoffmann, William L. Nyhan, W.O. Renier, J.A.M. Smeitink, Coriene E. Catsman‐Berrevoets, Ola Hjalmarson, Hilary Vallance, Katsuo Sugita, Constance M. Bowe, John T. Herrin, W. J. Craigen, Neil R.M. Buist, D S Brookfield, R. A. Chalmers	59
9	X-Linked Glycerol Kinase Deficiency in the Mouse Leads to Growth Retardation, Altered Fat Metabolism, Autonomous Glucocorticoid Secretion and Neonatal Death 1997 ·Human Molecular Genetics ·A.H.M. Mahbubul Huq, Rhonda S. Lovell, C N Ou, Arthur L. Beaudet, W. J. Craigen	58
10	Persistent glycolic aciduria in a healthy child with normal alanine‐glyoxylate aminotransferase activity 1996 ·Journal of Inherited Metabolic Disease ·W. J. Craigen	6
11	Structure and expression of mouse mitochondrial voltage dependent anion channel genes 1994 ·The American Journal of Human Genetics ·W. J. Craigen, Rhonda S. Lovell, Margaret J. Sampson	2
12	De novo proximal interstitial deletions of 14q: Cytogenetic and molecular investigations 1994 ·American Journal of Medical Genetics ·(unknown), Kent L. Anderson, (unknown), W. J. Craigen, James R. Lupski, Lisa G. Shaffer	27
13	Recent advances in peptide chain termination 1990 ·Molecular Microbiology ·W. J. Craigen, (unknown), C. Thomas Caskey	60
14	Ectopic correction of ornithine transcarbamylase deficiency in sparse fur mice. 1990 ·Journal of Biological Chemistry ·Stephen N. Jones, Markus Grompe, (unknown), Gábor Veres, W. J. Craigen, C. Thomas Caskey	42
15	Cloning and expression of a mammalian peptide chain release factor with sequence similarity to tryptophanyl-tRNA synthetases. 1990 ·Proceedings of the National Academy of Sciences ·(unknown), W. J. Craigen, D. Muzny, E Harlow, C. Thomas Caskey	44
16	Rapid and precise mapping of the Escherichia coli release factor genes by two physical approaches 1988 ·Journal of Bacteriology ·(unknown), Yuji Kohara, Kazufumi Akiyama, Cassandra L. Smith, W. J. Craigen, C. Thomas Caskey	23
17	The 5' flanking region of the ornithine transcarbamylase gene contains DNA sequences regulating tissue-specific expression. 1986 ·Journal of Biological Chemistry ·Gábor Veres, W. J. Craigen, C. Thomas Caskey	25

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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