Physician
Orthopaedic Surgery
Dr. Richard Straub, MD
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Dr. Richard Straub works in the field of Orthopaedic Surgery. He attended Georgetown University School of Medicine. Georgetown University School of Medicine is ranked 49/84 in Research/PrimaryCare. He received 1 awards: "CMS Meaningful Use Stage 1 Certification". Richard Straub is a published doctor and has 101 publications published. The lastest was: 'No linkage or linkage disequilibrium between brain-derived neurotrophic factor (BDNF) dinucleotide repeat polymorphism and schizophrenia in Irish families.' Richard Straub accepts Medicare.
Publications
- Characteristics of the Cation Cotransporter NKCC1 in Human Brain: Alternate Transcripts, Expression in Development, and Potential Relationships to Brain Function and S...
- Differential Effects of Common Variants in SCN2A on General Cognitive Ability, Brain Physiology, and messenger RNA Expression in Schizophrenia Cases and Control Indivi...
- Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
- Paternal age, de novo mutations and schizophrenia.
- Variation in psychosis gene ZNF804A is associated with a refined schizotypy phenotype but not neurocognitive performance in a large young male population.
- Schizophrenia Candidate Gene ERBB4: Covert Routes of Vulnerability to Psychosis Detected at the Population Level.
- Effect of Schizophrenia risk-associated alleles in SREB2 (GPR85) on functional MRI phenotypes in healthy volunteers.
- [Renal enhancement and excretion of the hepatobiliary contrast agent Gd-EOB-DTPA].
- [Electrodermal reactivity in schizophrenic women with so-called basic symptoms].
- Epidemiological and genetic study of exertional rhabdomyolysis in a Warmblood horse family in Switzerland.
- Genetic alterations of microsatellites on chromosome 18 in human breast carcinoma.
- Report and abstracts of the second international workshop on human chromosome 18 mapping. Doorwerth, the Netherlands, July 19-20, 1993.
- A microsatellite genetic linkage map of human chromosome 18.
- Expression cloning of a cDNA encoding the mouse pituitary thyrotropin-releasing hormone receptor.
- Bipolar disorder and linkage to Xq28.
- Thyrotropin-releasing hormone (TRH) and phorbol myristate acetate decrease TRH receptor messenger RNA in rat pituitary GH3 cells: evidence that protein kinase-C mediat...
- Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees.
- A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.
- GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
- HLA and schizophrenia: refutation of reported associations with A9 (A23/A24), DR4, and DQbeta1*0602.
- A schizophrenia locus may be located in region 10p15-p11.
- SETA is a multifunctional adapter protein with three SH3 domains that binds Grb2, Cbl, and the novel SB1 proteins.
- Allelic variation in GAD1 (GAD67) is associated with schizophrenia and influences cortical function and gene expression.
- fMRI evidence for functional epistasis between COMT and RGS4.
- A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborat...
- Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multip...
- The putative schizophrenia locus on chromosome 6p: a brief overview of the linkage studies.
- Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
- Reflections on the evidence for a vulnerability locus for schizophrenia on chromosome 6p24-22.
- Schizophrenia and HLA: No association with PCR-SSOP typed classical loci in a large Irish familial sample.
- Serious obstetric Complications interact with hypoxia-regulated/vascular-expression genes to influence schizophrenia risk.
- Neurotrophin-3 gene polymorphisms and schizophrenia: no evidence for linkage or association.
- Examination of new and reported data of the DRD3/MscI polymorphism: no support for the proposed association with schizophrenia.
- Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit fur...
- Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy.
- No association or linkage between the 5-HT2a/T102C polymorphism and schizophrenia in Irish families.
- An association study of DRD5 with smoking initiation and progression to nicotine dependence.
- No evidence to support the association of the potassium channel gene hSKCa3 CAG repeat with schizophrenia or bipolar disorder in the Irish population.
- No linkage or linkage disequilibrium between brain-derived neurotrophic factor (BDNF) dinucleotide repeat polymorphism and schizophrenia in Irish families.
- A 5'' promoter region SNP in NRG1 is associated with schizophrenia risk and type III isoform expression.
- GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss.
- Further evidence for association between ErbB4 and schizophrenia and influence on cognitive intermediate phenotypes in healthy controls.
- Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).
- Linkage of Niemann-Pick Disease type C to human chromosome 18.
- Support for schizophrenia vulnerability loci on chromosomes 6p and 8p from Irish families.
- A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.
- Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families.
- Haplotypes of four novel single nucleotide polymorphisms in the nicotinic acetylcholine receptor beta2-subunit (CHRNB2) gene show no association with smoking initiatio...
- BDNF Val66Met polymorphism significantly affects d'' in verbal recognition memory at short and long delays.
- Irish study on high-density schizophrenia families: field methods and power to detect linkage.
- Association of the tryptophan hydroxylase gene with smoking initiation but not progression to nicotine dependence.
- Marker-to-marker linkage disequilibrium on chromosomes 5q, 6p, and 8p in Irish high-density schizophrenia pedigrees.
- The trimmed-haplotype test for linkage disequilibrium.
- Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia.
- Analysis of epistasis in linked regions in the Irish study of high-density schizophrenia families.
- Expression analysis of neuregulin-1 in the dorsolateral prefrontal cortex in schizophrenia.
- Clinical features of psychotic disorders and polymorphisms in HT2A, DRD2, DRD4, SLC6A3 (DAT1), and BDNF: a family based association study.
- Sibling correlation of deficit Syndrome in the Irish study of high-density schizophrenia families.
- Clinical features of schizophrenia and linkage to chromosomes 5q, 6p, 8p, and 10p in the Irish Study of High-Density Schizophrenia Families.
- Resemblance of psychotic symptoms and Syndromes in affected sibling pairs from the Irish Study of High-Density Schizophrenia Families: evidence for possible etiologic ...
- Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families.
- Expression of GABA signaling molecules KCC2, NKCC1, and GAD1 in cortical development and schizophrenia.
- Evidence of sex-modulated association of ZNF804A with schizophrenia.
- Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.
- Genetic variation in CACNA1C affects brain circuitries related to mental illness.
- Genetic variation in FGF20 modulates hippocampal biology.
- Genetic modulation of GABA levels in the Anterior cingulate cortex by GAD1 and COMT.
- Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia.
- Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function.
- Genetic variation in AKT1 is linked to dopamine-associated prefrontal cortical structure and function in humans.
- Variants in the estrogen receptor alpha gene and its mRNA contribute to risk for schizophrenia.
- The evolutionarily conserved G protein-coupled receptor SREB2/GPR85 influences brain size, behavior, and vulnerability to schizophrenia.
- Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families.
- Evidence that the BLOC-1 protein dysbindin modulates dopamine D2 receptor internalization and signaling but not D1 internalization.
- Reduced DTNBP1 (dysbindin-1) mRNA in the hippocampal formation of schizophrenia patients.
- Alpha7 nicotinic acetylcholine receptor mRNA expression and binding in postmortem human brain are associated with genetic variation in neuregulin 1.
- Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls.
- Risk for premenstrual dysphoric disorder is associated with genetic variation in ESR1, the estrogen receptor alpha gene.
- Allelic variation in RGS4 impacts functional and structural connectivity in the human brain.
- Genetic evidence implicating DARPP-32 in human frontostriatal structure, function, and cognition.
- A genome-wide scan for modifier loci in schizophrenia.
- Variation in Disc1 affects hippocampal structure and function and increases risk for schizophrenia.
- Support for association between ADHD and two candidate genes: NET1 and DRD1.
- The brain-derived neurotrophic factor val66met polymorphism and variation in human cortical morphology.
- Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and Disc1: influence on risk of schizophrenia.
- RGS4 mRNA expression in postmortem human cortex is associated with COMT Val158Met genotype and COMT enzyme activity.
- Schizophrenia genes - famine to feast.
- Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples.
- Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the Disease.
- Effect of metabotropic glutamate receptor 3 genotype on N-acetylaspartate measures in the dorsolateral prefrontal cortex.
- The G72/G30 gene complex and cognitive abnormalities in schizophrenia.
- Expression of Disc1 binding partners is reduced in schizophrenia and associated with Disc1 SNPs.
- Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia.
- Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia.
- Human dysbindin (DTNBP1) gene expression in normal brain and in schizophrenic prefrontal cortex and midbrain.
- Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?
- Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified.
- Candidate genes for nicotine dependence via linkage, epistasis, and bioinformatics.
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.
- Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.
Schools
Georgetown University School Of Medicine
Boston University Med CtrUniv Hp
Procedures Preformed
- ACL (Anterior Cruciate Ligament) Surgery
- Carpal Tunnel Release
- Elbow Fracture and-or Dislocation Treatment, Closed
- Foot and Ankle Fracture Treatment, Open
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Conditions Treated
- Achilles Tendinitis
- Adhesive Capsulitis
- Ankle Fracture
- Ankle Sprain and Achilles Tendon Sprain or Rupture
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Doctors Specialties
- Orthopedic Surgery
- Orthopaedic Surgery
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Pathway X Bronze Direct CACA IN HIX
- Assurant Health
- Blue Card PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- Coventry Health Care
- Harvard Pilgrim Health Care PPO
- Choice Care PPO
- Mail Handlers Benefit Plan (MHBP)
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Tufts Health Plans
- Tufts PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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Boston University Medical Center -
Georgetown University School of Medicine
Drug Facts
| NPI NUMBER | 1861471393 | |
| NPPES Provider LastName | STRAUB | |
| NPPES Provider FirstName | RICHARD | |
| NPPES Provider ZIPCode | 030382752 | |
| NPPES Provider State | NH | |
| Specialty Description | Orthopedic Surgery | |
| Total Claim Count | 33.0 | |
| Distinct Opioid Count | 1.0 | |
| Opioid Claim Count | 15.0 | |
| Percent Opioid Claims | 45.45 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1861471393 |
| Last Name Of The Provider | STRAUB |
| First Name Of The Provider | RICHARD |
| View All |
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