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SANGITA BATISH, D.O.
D.O.
Internal Medicine Physician
NPI: 1245470749Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
20A10375(CA)
Research & Publications (20)
The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans.
PMID 19543269·Nat Genet·2009
8-other
Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
PMID 19405097·Hum Mutat·2009
5-case
High-throughput mutational analysis of TOR1A in primary dystonia.
PMID 19284587·BMC Med Genet·2009
8-other
Myotonic dystrophy type 2 with focal asymmetric muscle weakness and no electrical myotonia.
PMID 19208413·Muscle Nerve·2009
5-case
Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.
PMID 17436244·Am J Hum Genet·2007
8-other
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
PMID 17200671·Nat Genet·2007
8-other
In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome.
PMID 17096168·Neurogenetics·2007
5-case
Aprataxin (APTX) gene mutations resembling multiple system atrophy.
PMID 17049295·Parkinsonism Relat Disord·2007
5-case
GST genotype may modify clinical phenotype in patients with Fanconi anaemia.
PMID 16173971·Br J Haematol·2005
8-other
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
PMID 16116424·Nat Genet·2005
8-other
A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.
PMID 16084127·Mol Ther·2005
8-other
Anti-MuSK myasthenia gravis presenting with purely ocular findings.
PMID 15956173·Arch Neurol·2005
5-case
Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
PMID 15643609·Hum Mutat·2005
8-other
Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia.
PMID 15070707·Blood·2004
8-other
Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia.
PMID 14559878·J Natl Cancer Inst·2003
8-other
Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.
PMID 12552564·Hum Mutat·2003
4-observational
High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia.
PMID 12525204·Arch Otolaryngol Head Neck Surg·2003
8-other
A 20-year perspective on the International Fanconi Anemia Registry (IFAR).
PMID 12393516·Blood·2003
8-other
Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool.
PMID 12031647·Exp Hematol·2002
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 500 W HOSPITAL RD
FRENCH CAMP, CA 95231 - Phone
- (209) 468-6600
Quick Facts
- NPI
- 1245470749
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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