Published in Anesth Analg on January 25, 1969
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Measurements and models of electric fields in the in vivo human brain during transcranial electric stimulation. Elife (2017) 0.86
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Localization of visually evoked cortical activity in humans. J Physiol (1985) 0.83
Early optimization in finger dexterity of skilled pianists: implication of transcranial stimulation. BMC Neurosci (2013) 0.81
The "quasi-uniform" assumption in animal and computational models of non-invasive electrical stimulation. Brain Stimul (2012) 0.81
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EEG Driven tDCS Versus Bifrontal tDCS for Tinnitus. Front Psychiatry (2012) 0.80
Effects of cranial electrotherapy stimulation on resting state brain activity. Brain Behav (2012) 0.79
Effect of brain-to-skull conductivity ratio on EEG source localization accuracy. Biomed Res Int (2013) 0.78
Using transcranial direct-current stimulation (tDCS) to understand cognitive processing. Atten Percept Psychophys (2016) 0.78
Skull Defects in Finite Element Head Models for Source Reconstruction from Magnetoencephalography Signals. Front Neurosci (2016) 0.77
Simultaneous head tissue conductivity and EEG source location estimation. Neuroimage (2015) 0.77
The development and modelling of devices and paradigms for transcranial magnetic stimulation. Int Rev Psychiatry (2017) 0.75
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Outcomes in spasticity after repetitive transcranial magnetic and transcranial direct current stimulations. Neural Regen Res (2014) 0.75
Auditory steady state responses and cochlear implants: Modeling the artifact-response mixture in the perspective of denoising. PLoS One (2017) 0.75
A 3D finite-difference BiCG iterative solver with the Fourier-Jacobi preconditioner for the anisotropic EIT/EEG forward problem. Comput Math Methods Med (2014) 0.75
Alpha Power Predicts Persistence of Bistable Perception. Sci Rep (2017) 0.75
Feasibility of Equivalent Dipole Models for Electroencephalogram-Based Brain Computer Interfaces. Brain Sci (2017) 0.75
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. Hum Mol Genet (2000) 6.21
Frequency of 22q11 deletions in patients with conotruncal defects. J Am Coll Cardiol (1998) 3.86
Physical activity outcomes of CHAMPS II: a physical activity promotion program for older adults. J Gerontol A Biol Sci Med Sci (2001) 2.79
Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion. Am J Med Genet (1995) 2.70
"CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency? J Med Genet (1994) 2.69
Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net! Genet Med (2001) 2.57
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern. J Pediatr (1999) 2.38
A practical algorithm for solving dynamic membrane equations. IEEE Trans Biomed Eng (1978) 1.87
EEG electrode sensitivity--an application of reciprocity. IEEE Trans Biomed Eng (1969) 1.81
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22). Am J Hum Genet (2000) 1.78
Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching. J Am Coll Cardiol (2001) 1.75
Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion. Am J Med Genet (1999) 1.71
Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints. Cytogenet Cell Genet (1998) 1.70
Thirty-seven candidate genes for polycystic ovary syndrome: strongest evidence for linkage is with follistatin. Proc Natl Acad Sci U S A (1999) 1.68
Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene. Nat Genet (1995) 1.68
Risk factors for rapid repeat pregnancy among adolescent mothers: a review of the literature. J Pediatr Adolesc Gynecol (1998) 1.67
Cerebellar atrophy in a patient with velocardiofacial syndrome. J Med Genet (1995) 1.64
Preliminary phenotypic map of chromosome 4p16 based on 4p deletions. Am J Med Genet (1995) 1.55
Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region. Am J Med Genet (1994) 1.49
Classical Noonan syndrome is not associated with deletions of 22q11. Am J Med Genet (1995) 1.41
Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome). Arthritis Rheum (1997) 1.36
Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow. J Pediatr (2000) 1.35
Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes. Clin Immunol Immunopathol (1998) 1.29
cDNA cloning and characterization of a human sperm antigen (SPAG6) with homology to the product of the Chlamydomonas PF16 locus. Genomics (1999) 1.24
Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects. J Med Genet (2001) 1.24
Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2. Hum Mol Genet (1995) 1.21
Cloning and expression of primate Daxx cDNAs and mapping of the human gene to chromosome 6p21.3 in the MHC region. DNA Cell Biol (1997) 1.20
Targeted inhibition of the Hedgehog pathway in established malignant glioma xenografts enhances survival. Oncogene (2009) 1.16
Skeletal anomalies and deformities in patients with deletions of 22q11. Am J Med Genet (1997) 1.16
Fraction size in external beam radiation therapy in the treatment of melanoma. Int J Radiat Oncol Biol Phys (1991) 1.15
Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndrome. J Biol Chem (1996) 1.10
Antenatal diagnosis of DiGeorge syndrome. Lancet (1991) 1.08
The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development. Am J Hum Genet (1997) 1.07
Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). Clin Diagn Lab Immunol (1999) 1.03
On the independence of magnetic and electric body surface recordings. IEEE Trans Biomed Eng (1975) 1.01
Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype. Am J Hum Genet (1998) 1.01
More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated. Mol Syndromol (2013) 1.00
Induction of a heat shock gene at the site of tissue injury in the rat brain. Neuron (1989) 0.98
Humoral immunity in DiGeorge syndrome. J Pediatr (1995) 0.98
Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). Clin Diagn Lab Immunol (1998) 0.98
Chromosome 22q11 deletion in patients with truncus arteriosus. Pediatr Cardiol (2003) 0.98
The use of refusal postcards in recruiting older adults. Ann Behav Med (2000) 0.96
Latent hypoparathyroidism in children with conotruncal cardiac defects. Circulation (1996) 0.94
Response of cultured myocardial cells to countershock-type electric field stimulation. Am J Physiol (1978) 0.94
Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study. J Med Genet (2005) 0.92
Microdeletion 22q11.2: clinical data and deletion size. J Med Genet (1999) 0.92
Growth hormone deficiency in patients with 22q11.2 deletion: expanding the phenotype. Pediatrics (1998) 0.92
Local potential gradients as a unifying measure for thresholds of stimulation, standstill, tachyarrhythmia and fibrillation appearing after strong capacitor discharges. Adv Cardiol (1978) 0.91
Allelic variants of the follistatin gene in polycystic ovary syndrome. J Clin Endocrinol Metab (2000) 0.91
Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical region. Hum Mol Genet (1997) 0.90
Successful formation of a chimeric human thymus allograft following transplantation of cultured postnatal human thymus. J Immunol (1997) 0.90
Phenotypic characterization of the human fibrous histiocytoma giant cell tumor (GCT) cell line and its cytokine repertoire. Exp Hematol (1993) 0.90
Cerebrospinal fluid shunts in pregnancy. Report of two cases and review of the literature. Am J Perinatol (1988) 0.90
Inhibition of VIP-stimulated ion transport by a novel Y-receptor phenotype in rabbit distal colon. Am J Physiol (1993) 0.89
DiGeorge anomaly with renal agenesis in infants of mothers with diabetes. Am J Med Genet (1993) 0.88
Current density in bilateral and unilateral ECT. Biol Psychiatry (1976) 0.88
Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus. Cold Spring Harb Symp Quant Biol (1996) 0.87
Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome. Am J Med Genet (1997) 0.87
Treatment of aggressive keratoacanthomas by radiotherapy. J Am Acad Dermatol (1990) 0.87
The efficacy, tolerability, and safety of 1200 mg/d of oxaprozin and 1500 mg/d of nabumetone in the treatment of patients with osteoarthritis of the knee. Clin Ther (1997) 0.86
EMG to torque relationship in rectus abdominis muscle. Results with repeated testing. Spine (Phila Pa 1976) (1989) 0.85
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype. Am J Dis Child (1993) 0.84
Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence. Pediatrics (1997) 0.84
Developmental presentation of 22q11.2 deletion (DiGeorge/velocardiofacial syndrome). J Dev Behav Pediatr (1998) 0.83
Molecular cloning of calmodulin mRNA species which are preferentially expressed in neurons in the rat brain. Brain Res Mol Brain Res (1992) 0.83
Recognition of tubo-ovarian abscess in adolescents with pelvic inflammatory disease. J Adolesc Health (1996) 0.83
Seven new cases of Cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case. Am J Med Genet (1998) 0.82
Radiation therapy in cancer patients 80 years of age and older. Am J Clin Oncol (2000) 0.81
Communication disorders in the 22Q11.2 microdeletion syndrome. J Commun Disord (2000) 0.80
Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region. Eur J Pediatr Surg (1993) 0.80
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Early ultrasound diagnosis of Neu-Laxova syndrome. Prenat Diagn (2001) 0.79
Comparison of acoustic and electrical signals from erectores spinae muscles. Muscle Nerve (1988) 0.78
An inhomogeneous anisotropic model of the human torso for electrocardiographic studies. Med Biol Eng (1971) 0.78
Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2. Am J Med Genet (1996) 0.78
Qualitative effects of thoracic resistivity variations on the interpretation of electrocardiograms: the low resistance surface layer. Am Heart J (1968) 0.77
Quantitative comparison of pre-mortem ECG's with those reconstructed from activation data of a revived heart. J Electrocardiol (1980) 0.77
Current distribution from defibrillation electrodes in a homogeneous torso model. J Electrocardiol (1969) 0.77
Nasal dimple as part of the 22q11.2 deletion syndrome. Am J Med Genet (1997) 0.76
Unbalanced 15;22 translocation in a patient with manifestations of DiGeorge and velocardiofacial syndrome. Am J Med Genet (1997) 0.76
Stimulus parameters in electroconvulsive shock. J Psychiatr Res (1974) 0.75
Graphical evaluation of the spatial ventricular vector. Arch Kreislaufforsch (1966) 0.75
Optimisation of the locations of multiple-dipole heart generators in a simple torso model. Med Biol Eng Comput (1979) 0.75
Inhibition of the proteolytic contaminant in commercial xanthine oxidase preparations by serum protein fractions. J Free Radic Biol Med (1985) 0.75
Relationships among Green's theorem, Helmholtz' theorem, and integral equation methods of solving the forward ECG problem. IEEE Trans Biomed Eng (1978) 0.75
Normalisation of body impedance data: a theoretical study. Med Biol Eng Comput (1984) 0.75
Graphic studies concerning the body surface distribution of T potentials. Am Heart J (1972) 0.75
Prenatal diagnosis of the derivative chromosome 22 associated with cat eye syndrome by fluorescence in situ hybridization. Prenat Diagn (1994) 0.75
At one with death: destructive narcissism. Psychoanal Q (2000) 0.75
Theoretical analyses and computer simulation of ECG ventricular gradient and recovery waveforms. IEEE Trans Biomed Eng (1982) 0.75
The fiftieth anniversary of Dr. Lepeschkin's career. J Electrocardiol (1984) 0.75
Qualitative effects of thoracic resistivity variations on the interpretation of electrocardiograms: the "Brody" effect. Am Heart J (1967) 0.75
Trunk extensor EMG-torque relationship. Spine (Phila Pa 1976) (1987) 0.75
The complete heart-lead relationship in the Einthoven triangle. Bull Math Biophys (1968) 0.75
Inhomogeneities as a cause of multiple peaks of heart potential on the body surface: theoretical studies. IEEE Trans Biomed Eng (1971) 0.75
Attitudes of carers and the elderly occupants of residential homes to antimicrobial chewing gum as an aid to oral health. Br Dent J (1999) 0.75
Some quantitative estimates of inhomogeneity effects in electrocardiography. Am Heart J (1976) 0.75
Application of a muscle-potential monitor to electroconvulsive therapy. IEEE Trans Biomed Eng (1977) 0.75
Comparison of theoretical with measured forward ECG solutions: a progress report. Comput Biomed Res (1982) 0.75