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C. Gallione · SciRah

Researcher profile · Semantic Scholar

C. Gallione

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C. Gallione — researcher profile on SciRah

h-index: 34
Works: 57
Citations: 8,735

Most-cited papers

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
K. McAllister, K. Grogg, D. W. Johnson, C. Gallione +16 more
1994Nature Genetics1,605 citations Open access
Semantic Scholar
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
D. W. Johnson, J. Berg, M. A. Baldwin, C. Gallione +12 more
1996Nature Genetics1,131 citations
Semantic Scholar
Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
M. Shirley, Hao Tang, C. Gallione, Joseph D. Baugher +6 more
2013New England Journal of Medicine961 citations Open access
Semantic Scholar
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).
C. Gallione, G. Repetto, E. Legius, A. Rustgi +6 more
2004The Lancet791 citations
Semantic Scholar
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).
Trilochan Sahoo, E. W. Johnson, James W. Thomas, P. Kuehl +16 more
1999Human Molecular Genetics371 citations
Semantic Scholar
Nucleotide sequences of the mRNA's encoding the vesicular stomatitis virus G and M proteins determined from cDNA clones containing the complete coding regions
John K. Rose, C. Gallione
1981Journal of Virology329 citations Open access
Semantic Scholar
The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.
J. Berg, C. Gallione, T. Stenzel, David W. Johnson +5 more
1997American Journal of Human Genetics291 citations Open access
Semantic Scholar
SMAD4 mutations found in unselected HHT patients
C. Gallione, J. A. Richards, T. Letteboer, D. Rushlow +8 more
2006Journal of Medical Genetics255 citations Open access
Semantic Scholar
Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
K. Sweet, J. Willis, Xiao‐Ping Zhou, C. Gallione +15 more
2005Journal of the American Medical Association (JAMA)239 citations
Semantic Scholar
A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.
David W. Johnson, J. Berg, C. Gallione, Kimberly A. McAllister +6 more
1995Genome Research190 citations Open access
Semantic Scholar
A gene for familial venous malformations maps to chromosome 9p in a second large kindred.
C. Gallione, K. A. Pasyk, Laurence M. Boon, F. Lennon +6 more
1995Journal of Medical Genetics168 citations Open access
Semantic Scholar
Nucleotide sequences of the mRNA's encoding the vesicular stomatitis virus N and NS proteins
C. Gallione, J. Greene, L. Iverson, J. Rose
1981Journal of Virology162 citations Open access
Semantic Scholar
A single amino acid substitution in a hydrophobic domain causes temperature-sensitive cell-surface transport of a mutant viral glycoprotein
C. Gallione, John K. Rose
1985Journal of Virology159 citations Open access
Semantic Scholar
Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP–HHT syndrome
C. Gallione, A. Aylsworth, J. Beis, T. Berk +27 more
2010American Journal of Medical Genetics. Part A157 citations
Semantic Scholar
Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations
Jonathan Berg, M. Porteous, Diana Reinhardt, C. Gallione +6 more
2003Journal of Medical Genetics156 citations Open access
Semantic Scholar
Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis.
David A. McDonald, Chang-Bin Shi, R. Shenkar, C. Gallione +7 more
2014Human Molecular Genetics133 citations Open access
Semantic Scholar
The presence of cysteine in the cytoplasmic domain of the vesicular stomatitis virus glycoprotein is required for palmitate addition.
John K. Rose, Gregg A. Adams, C. Gallione
1984Proceedings of the National Academy of Sciences of the United States of America133 citations Open access
Semantic Scholar
Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia
S. Abdalla, C. Gallione, R. Barst, Evelyn M. Horn +4 more
2004European Respiratory Journal130 citations Open access
Semantic Scholar
Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations.
N. W. Plummer, C. Gallione, S. Srinivasan, J. Zawistowski +2 more
2004American Journal of Pathology123 citations Open access
Semantic Scholar
Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor function.
K. McAllister, Melanie A. Baldwin, A. Thukkani, C. Gallione +4 more
1995Human Molecular Genetics119 citations
Semantic Scholar
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Biallelic Loss of ENG or ACVRL1
D. Snellings, C. Gallione, D. Clark, N. Vozoris +2 more
2019bioRxiv115 citations Open access
Semantic Scholar
Nucleotide sequence of a cDNA clone encoding the entire glycoprotein from the New Jersey serotype of vesicular stomatitis virus
C. Gallione, John K. Rose
1983Journal of Virology114 citations Open access
Semantic Scholar
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles
C. Gallione, D. J. Klaus, Eric Y. Yeh, T. Stenzel +15 more
1998Human Mutation101 citations Open access
Semantic Scholar
RhoA Kinase Inhibition With Fasudil Versus Simvastatin in Murine Models of Cerebral Cavernous Malformations
R. Shenkar, Chang-Bin Shi, C. Austin, Thomas Moore +13 more
2016Stroke97 citations Open access
Semantic Scholar
Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanisms.
A. Lux, C. Gallione, D. Marchuk
2000Human Molecular Genetics68 citations
Semantic Scholar
Human Retroviral gag- and gag-pol-like Proteins Interact with the Transforming Growth Factor-β Receptor Activin Receptor-like Kinase 1*[boxs]
A. Lux, Christian Beil, Meher Majety, S. Barron +6 more
2005Journal of Biological Chemistry61 citations Open access
Semantic Scholar
Rho Kinase Inhibition Blunts Lesion Development and Hemorrhage in Murine Models of Aggressive Pdcd10/Ccm3 Disease
R. Shenkar, Amy Peiper, Heidy Pardo, Thomas Moore +15 more
2019Stroke56 citations Open access
Semantic Scholar
B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine Models
Chang-Bin Shi, R. Shenkar, H. Zeineddine, R. Girard +13 more
2016Journal of Neuroimmune Pharmacology48 citations Open access
Semantic Scholar
Novel murine models of cerebral cavernous malformations
Matthew R. Detter, R. Shenkar, Christian R Benavides, Catherine A. Neilson +11 more
2020Angiogenesis45 citations Open access
Semantic Scholar
Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effect
C. Gallione, Erin A. Scheessele, Diana Reinhardt, A. Duits +3 more
2000Human Genetics45 citations
Semantic Scholar
Propranolol inhibits cavernous vascular malformations by β1 adrenergic receptor antagonism in animal models.
Wen-Qing Li, R. Shenkar, Mathew R. Detter, Thomas Moore +12 more
2021Journal of Clinical Investigation39 citations Open access
Semantic Scholar
A Brain Targeted Orally Available ROCK2 Inhibitor Benefits Mild and Aggressive Cavernous Angioma Disease
L. Mckerracher, R. Shenkar, Matthew Abbinanti, Ying Cao +12 more
2019Translational Stroke Research37 citations Open access
Semantic Scholar
Novel missense and frameshift mutations in the activin receptor‐like kinase‐1 gene in hereditary hemorrhagic telangiectasia
D. J. Klaus, C. Gallione, K. Anthony, Eric Y. Yeh +4 more
199835 citations
Semantic Scholar
Micro-Computed Tomography in Murine Models of Cerebral Cavernous Malformations as a Paradigm for Brain Disease
R. Girard, H. Zeineddine, Courtney P Orsbon, H. Tan +16 more
2016Journal of Neuroscience Methods34 citations Open access
Semantic Scholar
A novel somatic mutation in GNAQ in a capillary malformation provides insight into molecular pathogenesis
F. Galeffi, D. Snellings, S. Wetzel-Strong, N. Kastelic +4 more
2022Angiogenesis33 citations Open access
Semantic Scholar
Phenotypic Characterization of Murine Models of Cerebral Cavernous Malformations
H. Zeineddine, R. Girard, Laleh Saadat, Le Shen +18 more
2018Laboratory Investigation28 citations Open access
Semantic Scholar
Natural Genetic Variation of Integrin Alpha L (Itgal) Modulates Ischemic Brain Injury in Stroke
Sehoon Keum, H. Lee, Pei-Lun Chu, Matthew J. Kan +5 more
2013PLoS Genetics28 citations Open access
Semantic Scholar
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesis.
E. DeBose-Scarlett, Andrew K. Ressler, C. Gallione, Gonzalo Sapisochin Cantis +8 more
2024American Journal of Human Genetics23 citations Open access
Semantic Scholar
Developmental Expression of the Sturge-Weber Syndrome-associated Genetic Mutation in Gnaq: a Formal Test of Happle's Paradominant Inheritance Hypothesis.
S. Wetzel-Strong, F. Galeffi, Christian R Benavides, Mary Patrucco +4 more
2023Genetics21 citations Open access
Semantic Scholar
A founder mutation in the Ashkenazi Jewish population affecting mRNA splicing of the CCM2 gene is associated with Cerebral Cavernous Malformations
C. Gallione, Ann Solatycki, I. Awad, J. Weber +1 more
2011Genetics in Medicine17 citations Open access
Semantic Scholar
Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia
I. Svenson, M. Kloos, Amy Jacon, C. Gallione +4 more
2005Neurogenetics17 citations
Semantic Scholar
Propranolol as therapy for cerebral cavernous malformations: a cautionary note
R. Shenkar, Thomas Moore, Christian R Benavides, R. Lightle +9 more
2022Journal of Translational Medicine14 citations Open access
Semantic Scholar
Single-nucleus DNA sequencing reveals hidden somatic loss-of-heterozygosity in Cerebral Cavernous Malformations
Andrew K. Ressler, D. Snellings, R. Girard, C. Gallione +4 more
2023Nature Communications12 citations Open access
Semantic Scholar
Propranolol inhibits cavernous vascular malformations by β1 adrenergic receptor antagonism.
Wen-Qing Li, R. Shenkar, Matthew R. Detter, Thomas Moore +12 more
2020Journal of Clinical Investigation11 citations Open access
Semantic Scholar
EXCEPTIONAL AGGRESSIVENESS OF CEREBRAL CAVERNOUS MALFORMATION DISEASE ASSOCIATED WITH PDCD10 MUTATIONS
R. Shenkar, Chang-Bin Shi, T. Rebeiz, Rebecca A. Stockton +13 more
2014Genetics in Medicine11 citations Open access
Semantic Scholar
Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online.
D. J. Klaus, C. Gallione, K. Anthony, Eric Y. Yeh +4 more
1998Human Mutation9 citations
Semantic Scholar
Quantitative DNA pooling to increase the efficiency of linkage analysis in autosomal dominant disease
K. Damji, C. Gallione, R. Allingham, Brandon D. Slotterbeck +6 more
1998Human Genetics7 citations
Semantic Scholar
Novel hemorrhage models of cerebral cavernous malformations
Matthew R. Detter, R. Shenkar, Christian R Benavides, Catherine A. Neilson +11 more
2020bioRxiv4 citations Open access
Semantic Scholar
Genetic genealogy uncovers a founder deletion mutation in the Cerebral Cavernous Malformations 2 gene
C. Gallione, Matthew R. Detter, Adrienne Sheline, Henrietta M Christmas +2 more
2021Human Genetics3 citations Open access
Semantic Scholar
Juvenile stroke in combined syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis
S. Mazzucco, L. Benini, C. Gallione, P. d'Adamo +1 more
2014Neurological Sciences3 citations
Semantic Scholar

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