William J. Craigen

15.0k citations

104 papers · 6.8k indexed · 2 hit papers · h-index 41

Molecular Biology top 1%
Clinical Biochemistry top 0.1%
Cardiology and Cardiovascular Medicine top 2%
Genetics top 2%
Physiology top 5%

Co-authors: Tatiana Sheiko Christopher Baines Jeffery D. Molkentin Robert A. Kaiser Margaret J. Sampson Emily H. Cheng Jill K. Fisher Stanley J. Korsmeyer
Topics: Mitochondrial Function and Pathology (58 papers)Metabolism and Genetic Disorders (38 papers)ATP Synthase and ATPases Research (19 papers)
Cited by: Clinical Biochemistry Molecular Biology Genetics
Journals: Science Cell Proceedings of the National Academy of Sciences
Partner nations: United States Canada Netherlands

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

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

#	Work	Indexed citations
1	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 2023 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Rebecca Schultz,Elaine Seto,(unknown),William J. Craigen,John W. Swann,Mingshan Xue,Hsiao‐Tuan Chao	4
2	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 2021 ·Genetics in Medicine ·Cindy Li,Ankit K. Desai,Punita Gupta,(unknown),Vikas Bhambhani,Robert J. Hopkin,Can Fıçıcıoğlu,Pranoot Tanpaiboon,William J. Craigen,Amy S. Rosenberg,Priya S. Kishnani	33
3	A novel de novo intronic variant in ITPR1 causes Gillespie syndrome 2021 ·American Journal of Medical Genetics Part A ·(unknown),Ming‐Ming Jiang,Xiaohui Li,Ronit Marom,Hongzheng Dai,David R. Murdock,Pengfei Liu,Jill V. Hunter,Jason D. Heaney,Laurie Robak,Lisa Emrick,Timothy Lotze,Lauren S. Blieden,(unknown),Richard A. Lewis,Alex V. Levin,Jenina Capasso,William J. Craigen,Jill A. Rosenfeld,Brendan Lee,Lindsay C. Burrage	5
4	Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated Propionylcarnitine 2016 ·JIMD Reports ·Gerarda Cappuccio,Paldeep S. Atwal,Taraka Donti,(unknown),(unknown),William J. Craigen,V. Reid Sutton,Sarah H. Elsea	6
5	Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing 2016 ·Journal of Molecular Diagnostics ·Lan Qin,Jing Wang,Tian Xia,(unknown),Cavatina K. Truong,John J. Mitchell,Klaas J. Wierenga,William J. Craigen,Victor Wei Zhang,Lee‐Jun C. Wong	66
6	The GABA Transaminase, ABAT, Is Essential for Mitochondrial Nucleoside Metabolism 2015 ·Cell Metabolism ·Arnaud Besse,Ping Chun Wu,Francesco Bruni,Taraka Donti,Brett H. Graham,William J. Craigen,Robert McFarland,Paolo Moretti,Seema R. Lalani,Kenneth L. Scott,Robert W. Taylor,Penelope E. Bonnen	112
7	Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes 2013 ·Molecular Genetics and Metabolism ·(unknown),Jing Wang,Guoli Wang,Soledad Kleppe,Victor Wei Zhang,Eric Schmitt,William J. Craigen,Deborah L. Renaud,Qin Sun,Lee‐Jun Wong	29
8	Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review 2012 ·Human Pathology ·Pilar Magoulas,Ayman W. El‐Hattab,Angshumoy Roy,Deeksha Bali,Milton J. Finegold,William J. Craigen	21
9	Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin 2012 ·Genetics in Medicine ·Jing Wang,Hong Cui,Ni‐Chung Lee,Wuh‐Liang Hwu,Yin‐Hsiu Chien,William J. Craigen,Lee‐Jun C. Wong,Victor Wei Zhang	53
10	An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory’s experience 2012 ·Genetics in Medicine ·Jing Wang,Eric Schmitt,Megan Landsverk,Victor Wei Zhang,Fangyuan Li,Brett H. Graham,William J. Craigen,Lee‐Jun C. Wong	30
11	Dilation of the aortic root in mitochondrial disease patients 2011 ·Molecular Genetics and Metabolism ·Nicola Brunetti‐Pierri,Ricardo H. Pignatelli,(unknown),Jeffrey A. Towbin,John W. Belmont,William J. Craigen,Lee‐Jun Wong,John L. Jefferies,Fernando Scaglia	19
12	Voltage-dependant anion channels: Novel insights into isoform function through genetic models 2011 ·Biochimica et Biophysica Acta (BBA) - Biomembranes ·(unknown),Tatiana Sheiko,Brett H. Graham,William J. Craigen	72
13	MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations 2009 ·Molecular Genetics and Metabolism ·Ayman W. El‐Hattab,(unknown),Eric Schmitt,Shulin Zhang,William J. Craigen,Lee-Jun Wong	59
14	Novel cardiac findings in periventricular nodular heterotopia 2009 ·American Journal of Medical Genetics Part A ·John L. Jefferies,Michael D. Taylor,Joseph W. Rossano,John W. Belmont,William J. Craigen	12
15	Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation 2006 ·The American Journal of Human Genetics ·Seema R. Lalani,(unknown),Susan Fernbach,Karine G. Harutyunyan,Christina Thaller,L. E. Peterson,John D. McPherson,Richard A. Gibbs,Lisa D. White,Margaret A. Hefner,Sandra L. H. Davenport,John M. Graham,Carlos A. Bacino,Nancy L. Glass,Jeffrey A. Towbin,William J. Craigen,Steven R. Neish,Angela E. Lin,John W. Belmont	264
16	Properties of the permeability transition in VDAC1−/− mitochondria 2006 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Alexandra Krauskopf,Ove Eriksson,William J. Craigen,Michael Forte,Paolo Bernardi	177
17	A Novel Isoform of the Mitochondrial Outer Membrane Protein VDAC3 via Alternative Splicing of a 3-Base Exon 1998 ·Journal of Biological Chemistry ·Margaret J. Sampson,Lyle O. Ross,William K. Decker,William J. Craigen	50
18	Regional localization of the mouse argininosuccinate lyase gene to Chromosome 5 1997 ·Mammalian Genome ·(unknown),Yanzhen Pan,William J. Craigen	2
19	Isolation, Mapping, and Functional Expression of the Mouse X Chromosome Glycerol Kinase Gene 1996 ·Genomics ·A.H.M. Mahbubul Huq,Rhonda S. Lovell,Margaret J. Sampson,William K. Decker,Mary Beth Dinulos,Christine M. Distèche,William J. Craigen	19
20	d-2-Hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction 1994 ·Pediatric Neurology ·William J. Craigen,Cornelis Jakobs,Elizabeth A. Sekul,Moise L. Levy,K. Michael Gibson,Ian J. Butler,Gail E. Herman	26

About William J. Craigen

William J. Craigen is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry, having authored 104 papers that have together received 6.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (58 papers), Metabolism and Genetic Disorders (38 papers) and ATP Synthase and ATPases Research (19 papers). The work is most often cited by research in Clinical Biochemistry (1.3k citations), Molecular Biology (5.1k citations) and Genetics (571 citations). William J. Craigen has collaborated with scholars based in United States, Canada and Netherlands. Frequent 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. Their work appears in journals such as Science, Cell and Proceedings of the National Academy of Sciences.

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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