William J. Craigen

15.0k total citations · 2 hit papers
104 papers, 6.8k citations indexed

About

William J. Craigen is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, William J. Craigen has authored 104 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 38 papers in Clinical Biochemistry and 16 papers in Genetics. Recurrent topics in William J. Craigen's work include Mitochondrial Function and Pathology (58 papers), Metabolism and Genetic Disorders (38 papers) and ATP Synthase and ATPases Research (19 papers). William J. Craigen is often cited by papers focused on Mitochondrial Function and Pathology (58 papers), Metabolism and Genetic Disorders (38 papers) and ATP Synthase and ATPases Research (19 papers). William J. Craigen collaborates with scholars based in United States, Canada and Netherlands. William J. Craigen's co-authors include Tatiana Sheiko, Christopher Baines, Jeffery D. Molkentin, Robert A. Kaiser, Margaret J. Sampson, Emily H. Cheng, Jill K. Fisher, Stanley J. Korsmeyer, John W. Belmont and Brett H. Graham and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

William J. Craigen

103 papers receiving 6.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death

2007 759 citations Tatiana Sheiko, William J. Craigen et al. profile →
VDAC2 Inhibits BAK Activation and Mitochondrial Apoptosis

2003 664 citations Tatiana Sheiko, William J. Craigen et al. profile →

Peers

William J. Craigen

CCM

GENET

PHYSI

Marjan Huizing United States

Miguel A. Martı́n Spain

Yoichi Matsubara Japan

Eduardo Bonilla United States

Lee‐Jun C. Wong United States

Ann Saada Israel

Sara Shanske United States

Armand F. Miranda United States

Brage Storstein Andresen Denmark

Robert Kleta United Kingdom

Marjan Huizing United States

William J. Craigen

3.1k ×0.6

848 ×0.6

336 ×0.4

CCM

628 ×0.7

GENET

676 ×1.1

PHYSI

Citations per year, relative to William J. Craigen William J. Craigen (= 1×) peers Marjan Huizing

Countries citing papers authored by William J. Craigen

Since Specialization

Citations

This map shows the geographic impact of William 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 William 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 William J. Craigen more than expected).

Fields of papers citing papers by William J. Craigen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of William J. Craigen. A scholar is included among the top collaborators of William 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 William J. Craigen. William 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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20 of 20 papers shown

Schultz, Rebecca, Elaine Seto, William J. Craigen, et al.. (2023). PAK1 c.1409 T > a (p. Leu470Gln) de novo variant affects the protein kinase domain, leading to epilepsy, macrocephaly, spastic quadriplegia, and hydrocephalus: Case report and review of the literature. American Journal of Medical Genetics Part A. 191(6). 1619–1625. 4 indexed citations

Li, Cindy, Ankit K. Desai, Punita Gupta, et al.. (2021). Transforming the clinical outcome in CRIM-negative infantile Pompe disease identified via newborn screening: the benefits of early treatment with enzyme replacement therapy and immune tolerance induction. Genetics in Medicine. 23(5). 845–855. 33 indexed citations

Jiang, Ming‐Ming, Xiaohui Li, Ronit Marom, et al.. (2021). A novel de novo intronic variant in ITPR1 causes Gillespie syndrome. American Journal of Medical Genetics Part A. 185(8). 2315–2324. 5 indexed citations

Cappuccio, Gerarda, Paldeep S. Atwal, Taraka Donti, et al.. (2016). Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine. JIMD Reports. 35. 33–37. 6 indexed citations

Qin, Lan, Jing Wang, Tian Xia, et al.. (2016). Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing. Journal of Molecular Diagnostics. 18(3). 446–453. 66 indexed citations

Besse, Arnaud, Ping Chun Wu, Francesco Bruni, et al.. (2015). The GABA Transaminase, ABAT, Is Essential for Mitochondrial Nucleoside Metabolism. Cell Metabolism. 21(3). 417–427. 112 indexed citations

Wang, Jing, Guoli Wang, Soledad Kleppe, et al.. (2013). Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes. Molecular Genetics and Metabolism. 109(3). 260–268. 29 indexed citations

Magoulas, Pilar, Ayman W. El‐Hattab, Angshumoy Roy, et al.. (2012). Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review. Human Pathology. 43(6). 943–951. 21 indexed citations

Wang, Jing, Hong Cui, Ni‐Chung Lee, et al.. (2012). Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin. Genetics in Medicine. 15(2). 106–114. 53 indexed citations

10.

Wang, Jing, Eric Schmitt, Megan Landsverk, et al.. (2012). An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory’s experience. Genetics in Medicine. 14(6). 620–626. 30 indexed citations

11.

Brunetti‐Pierri, Nicola, Ricardo H. Pignatelli, Jeffrey A. Towbin, et al.. (2011). Dilation of the aortic root in mitochondrial disease patients. Molecular Genetics and Metabolism. 103(2). 167–170. 19 indexed citations

12.

Sheiko, Tatiana, et al.. (2011). Voltage-dependant anion channels: Novel insights into isoform function through genetic models. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1818(6). 1477–1485. 72 indexed citations

13.

El‐Hattab, Ayman W., et al.. (2009). MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations. Molecular Genetics and Metabolism. 99(3). 300–308. 59 indexed citations

14.

Jefferies, John L., Michael D. Taylor, Joseph W. Rossano, John W. Belmont, & William J. Craigen. (2009). Novel cardiac findings in periventricular nodular heterotopia. American Journal of Medical Genetics Part A. 152A(1). 165–168. 12 indexed citations

15.

Lalani, Seema R., Susan Fernbach, Karine G. Harutyunyan, et al.. (2006). Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation. The American Journal of Human Genetics. 78(2). 303–314. 264 indexed citations

16.

Krauskopf, Alexandra, Ove Eriksson, William J. Craigen, Michael Forte, & Paolo Bernardi. (2006). Properties of the permeability transition in VDAC1−/− mitochondria. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1757(5-6). 590–595. 177 indexed citations

17.

Sampson, Margaret J., Lyle O. Ross, William K. Decker, & William J. Craigen. (1998). A Novel Isoform of the Mitochondrial Outer Membrane Protein VDAC3 via Alternative Splicing of a 3-Base Exon. Journal of Biological Chemistry. 273(46). 30482–30486. 50 indexed citations

18.

Pan, Yanzhen, et al.. (1997). Regional localization of the mouse argininosuccinate lyase gene to Chromosome 5. Mammalian Genome. 8(11). 871–871. 2 indexed citations

19.

Huq, A.H.M. Mahbubul, Rhonda S. Lovell, Margaret J. Sampson, et al.. (1996). Isolation, Mapping, and Functional Expression of the Mouse X Chromosome Glycerol Kinase Gene. Genomics. 36(3). 530–534. 19 indexed citations

20.

Craigen, William J., Cornelis Jakobs, Elizabeth A. Sekul, et al.. (1994). d-2-Hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction. Pediatric Neurology. 10(1). 49–53. 26 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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