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WILLIAM CRAIGEN, MD
MD
Pediatrics Physician
NPI: 1407936842IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
H9460(TX)
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
H9460(TX)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Additional
PEDIATRIC MEDICINE
Education
BAYLOR COLLEGE OF MEDICINE
Class of 1988
Research & Publications (20)
Genetic strategies for dissecting mammalian and Drosophila voltage-dependent anion channel functions.
PMID 18622693·J Bioenerg Biomembr·2008
6-review
Nek1 regulates cell death and mitochondrial membrane permeability through phosphorylation of VDAC1.
PMID 19158487·Cell Cycle·2009
7-preclinical
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
PMID 19064609·Hum Mol Genet·2009
8-other
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.
PMID 19188198·J Med Genet·2009
5-case
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
PMID 19471977·Neurogenetics·2009
5-case
Requirement of voltage-dependent anion channel 2 for pro-apoptotic activity of Bax.
PMID 19617898·Oncogene·2009
7-preclinical
A maxi-chloride channel in the inner membrane of mammalian mitochondria.
PMID 18805391·Biochim Biophys Acta·2008
7-preclinical
Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.
PMID 18205204·Hum Mutat·2008
8-other
Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.
PMID 17916097·Clin Genet·2007
5-case
VDAC1 serves as a mitochondrial binding site for hexokinase in oxidative muscles.
PMID 17207767·Biochim Biophys Acta·2007
7-preclinical
Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death.
PMID 17417626·Nat Cell Biol·2007
7-preclinical
Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.
PMID 17694548·Hepatology·2007
5-case
Two familial cases of high blood galactose of unknown aetiology.
PMID 16988899·J Inherit Metab Dis·2006
5-case
Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
PMID 17172942·Genet Med·2006
5-case
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
PMID 16400610·Am J Hum Genet·2006
7-preclinical
A severe case of dentatorubro-pallidoluysian atrophy (DRPLA) with microcephaly, very early onset of seizures, and cerebral white matter involvement.
PMID 17236112·Neuropediatrics·2006
5-case
Genetic demonstration that the plasma membrane maxianion channel and voltage-dependent anion channels are unrelated proteins.
PMID 16291750·J Biol Chem·2006
7-preclinical
Tissue-dependent alterations in lipid mass in mice lacking glycerol kinase.
PMID 15957255·Lipids·2005
4-observational
New insights into the mechanism of permeation through large channels.
PMID 16199505·Biophys J·2005
7-preclinical
Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy.
PMID 16246949·Circulation·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6701 FANNIN ST
HOUSTON, TX 77030 - Phone
- (832) 822-4280
Quick Facts
- NPI
- 1407936842
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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