Professor, Neurology, UCLA School of Medicine
Neurology
Dr. Joanna C. Jen, MD
|
|
Give Review
Doctor Joanna C. Jen, MD is an expert in the field of Neurology. She attended Yale University School of Medicine. Yale University School of Medicine is a top medical college. Yale University School of Medicine has a rank of 7 in research and a 57 in primary care She received 1 awards: "Super Doctor". Joanna C. Jen has written publications. She has 100 publications published with PubMed. The lastest publication is: 'Serial analysis of gene expression in non-small cell lung cancer.' She accepts Medicare payments and is registered with Medicare.gov.
Publications
- Evolution of Brain lesions in a patient with TREX1 cerebroretinal vasculopathy.
- Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
- Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.
- Neuronal voltage-gated calcium channels: brief overview of their function and clinical implications in neurology.
- Bilateral vestibulopathy: clinical, diagnostic, and genetic considerations.
- Familial episodic Ataxia: a model for migrainous vertigo.
- Episodic Ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
- Phenotypic and genetic analysis of a large family with Migraine-associated vertigo.
- Hereditary episodic Ataxias.
- Novel mutation in KCNA1 causes episodic Ataxia with paroxysmal dyspnea.
- C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with Cerebral leukodystrophy.
- Association of progesterone receptor with Migraine-associated vertigo.
- A new episodic Ataxia syndrome with linkage to chromosome 19q13.
- Blessed are the pacemakers.
- Three brothers with a very-late-onset writer's cramp.
- Nonconsensus intronic mutations cause episodic Ataxia.
- A novel mutation in KCNA1 causes episodic Ataxia without myokymia.
- Mutations in a human ROBO gene disrupt hindBrain axon pathway crossing and morphogenesis.
- No mutations in CACNA1A and ATP1A2 in probands with common types of Migraine.
- Chronic cough due to Thr124Met mutation in the Peripheral myelin protein zero (MPZ gene).
- Ocular motility in genetically defined autosomal dominant cerebellar Ataxia.
- Genetics of familial episodic vertigo and Ataxia.
- Genetics of episodic Ataxia.
- A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset Dystonia-parkinsonism.
- A genome-wide linkage scan of familial benign recurrent Vertigo: linkage to 22q12 with evidence of heterogeneity.
- Genetics of vestibulopathies.
- Recent advances in the genetics of recurrent Vertigo and vestibulopathy.
- Functional neuroanatomy of the human premotor oculomotor Brainstem nuclei: insights from postmortem and advanced in vivo imaging studies.
- Progressive cerebellar Ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation.
- Effects of failure of development of crossing Brainstem pathways on ocular motor control.
- Late-onset pure cerebellar Ataxia: differentiating those with and without identifiable mutations.
- Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2.
- Neurotological findings in a family with episodic Ataxia.
- Similar oculomotor phenotypes in episodic Ataxia type 2 and spinocerebellar atrophy type 6.
- A novel nonsense mutation in CACNA1A causes episodic Ataxia and hemiplegia.
- Mutation in the glutamate transporter EAAT1 causes episodic Ataxia, hemiplegia, and seizures.
- CACNA1A mutations causing episodic and progressive Ataxia alter channel trafficking and kinetics.
- Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene.
- Genetic heterogeneity of autosomal dominant nonprogressive congenital Ataxia.
- Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy.
- Clinical spectrum of episodic Ataxia type 2.
- Oculomotor phenotypes in autosomal dominant Ataxias.
- Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformation.
- Internuclear ophthalmoparesis in episodic Ataxia type 2.
- Temporal bone histopathology in dominantly inherited audiovestibular syndrome.
- Episodic vertical oscillopsia with progressive gait Ataxia: clinical description of a new episodic syndrome and evidence of linkage to chromosome 13q.
- Familial Migraine with vertigo: no mutations found in CACNA1A.
- De novo mutation in CACNA1A caused acetazolamide-responsive episodic Ataxia.
- Progressive Ataxia due to a missense mutation in a calcium-channel gene.
- Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
- Familial benign recurrent Vertigo.
- Spinocerebellar Ataxia type 6 with positional vertigo and acetazolamide responsive episodic Ataxia.
- Episodic Ataxia type 1 with distal weakness: a novel manifestation of a potassium channelopathy.
- Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS).
- Prolonged hemiplegic episodes in children due to mutations in ATP1A2.
- Slowing of voluntary and involuntary saccades: an early sign in spinocerebellar Ataxia type 7.
- Primary episodic Ataxias: diagnosis, pathogenesis and treatment.
- A randomized trial of 4-aminopyridine in EA2 and related familial episodic Ataxias.
- Diffusion tensor MRI shows abnormal Brainstem crossing fibers associated with ROBO3 mutations.
- Adult-onset hemiplegic Migraine with cortical enhancement and oedema.
- Differential subcellular immunolocalization of voltage-gated calcium channel alpha1 subunits in the chinchilla cristae ampullaris.
- Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25.
- Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2.
- Ataxia and calcium channels: what a headache!
- Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromos...
- Genomic organization and mutation analysis of Hel-N1 in lung Cancers with chromosome 9p21 deletions.
- White matter fiber tractography and color mapping of the normal human cerebellum with diffusion tensor imaging.
- Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3.
- Calcium channelopathies in the central Nervous system.
- AIS is an oncogene amplified in squamous cell carcinoma.
- Facile detection of mitochondrial DNA mutations in tumors and bodily fluids.
- Detecting colorectal Cancer in stool with the use of multiple genetic targets.
- Two distinct regions of loss on chromosome arm 4q in primary head and neck squamous cell carcinoma.
- Frequent gain of the p40/p51/p63 gene locus in primary head and neck squamous cell carcinoma.
- Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors.
- Mismatch repair gene defects in sporadic colorectal Cancers with microsatellite instability.
- Molecular detection of genetic alterations in the serum of colorectal Cancer patients.
- Rare loss-of-function mutation of a death receptor gene in head and neck Cancer.
- Distinguishing second primary tumors from lung metastases in patients with head and neck squamous cell carcinoma.
- Absence of TSG101 transcript abnormalities in human Cancers.
- Mutation analysis of hBUB1 in aneuploid HNSCC and lung Cancer cell lines.
- Microsatellite instability at AAAG repeat sequences in respiratory tract Cancers.
- Clues to the pathogenesis of familial colorectal Cancer.
- Methylation status in the promoter region of the human PGP9.5 gene in Cancer and normal tissues.
- Loss of chromosome arms 3p and 9p and inactivation of P16 (INK4a) in normal epithelium of patients with primary lung Cancer.
- Circulating antibodies to p40(AIS) in the sera of respiratory tract Cancer patients.
- Mutations of a mutS homolog in hereditary nonpolyposis colorectal Cancer.
- PGP9.5 as a candidate tumor marker for non-small-cell lung Cancer.
- Promoter hypermethylation patterns of p16, O6-methylguanine-DNA-methyltransferase, and death-associated protein kinase in tumors and saliva of head and neck Cancer pat...
- Chromosomal alterations in lung adenocarcinoma from smokers and nonsmokers.
- A new human p53 homologue.
- Frequent inactivation of PTEN/MMAC1 in primary prostate Cancer.
- Complete nucleotide sequence and identification of a putative promoter region for the expression in Escherichia coli of the cryIA(b) gene from Bacillus thuringiensis v...
- Hypermutability and mismatch repair deficiency in RER+ tumor cells.
- Molecular detection of tumor cells in bronchoalveolar lavage fluid from patients with early stage lung Cancer.
- GNB1L, a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein beta-subunit-like polypeptide.
- Gene promoter hypermethylation in tumors and serum of head and neck Cancer patients.
- Serial analysis of gene expression in non-small cell lung Cancer.
- An overview on the isolation and analysis of circulating tumor DNA in plasma and serum.
Schools
Yale University
Oreg Health Scis University
UCLA School Med
Procedures Preformed
- EEG (Electroencephalogram)
Conditions Treated
- Ataxia
- Brain and Nervous System Cancer (incl. Gliomas, Astrocytoma, Schwannoma, Medulloblastoma, Chordoma)
- Cerebral Artery Thrombosis
- Cerebrovascular Disease
- View All
Doctors Specialties
- Neurology
Accepted Insurances
Awards
- Super Doctor
Education
-
UCLA Medical Center -
Oregon Health & Science University -
Yale University School of Medicine
Hospital
-
Ronald Reagan UCLA Medical Center
Drug Facts
| NPI NUMBER | 1407879216 | |
| NPPES Provider LastName | JEN | |
| NPPES Provider FirstName | JOANNA | |
| NPPES Provider ZIPCode | 90095 | |
| NPPES Provider State | CA | |
| Specialty Description | Neurology | |
| Total Claim Count | 26.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1407879216 |
| Last Name Of The Provider | JEN |
| First Name Of The Provider | JOANNA |
| View All |
Similar Doctors
|
|
Dr. Antonio V. Escueta, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Jeremy D. Rudnick, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Charles C. Flippen, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Callene A. Momtazee, MD |
|
|
Dr. Robert C. Collins, MD |
|
|
Dr. Christine B. Baca, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Pantea Sharifi-Hannauer, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Daniel W. Chang, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Matthew J. Ashley, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Elliot J. Hogg, MD |
|
|
Dr. Po-Haong Lu, PHD |
|
|
Dr. Michael Su, MD
This Doctor is OpenDoctor Recommended.
|