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INGRID ROIG, M.D
M.D
Infectious Disease Physician
NPI: 1881847002IndividualAccepts Medicare
Specialties, Licenses & Credentials
Infectious Disease PhysicianPrimary
Internal Medicine — Infectious Disease
Code: 207RI0200X
31538(AL)
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
31538(AL)
CMS Specialties
PrimaryINFECTIOUS DISEASE
Education
OTHER
Class of 2004
Research & Publications (16)
Maternal origin of the human aneuploidies. Are homolog synapsis and recombination to blame? Notes (learned) from the underbelly.
PMID 18948712·Genome Dyn·2009
6-review
[Relationship between reticulated platelets and megacaryocyte number in thrombocytopenic patients].
PMID 19515392·Med Clin (Barc)·2009
8-other
Analysis of recombination along chromosome 21 during human female pachytene stage.
PMID 19490782·Reprod Biomed Online·2009
8-other
H. pylori eradication does not reduce paraprotein levels in monoclonal gammopathy of unknown significance (MGUS): a prospective cohort study.
PMID 19159929·Ann Hematol·2009
3-trial
ATR, BRCA1 and gammaH2AX localize to unsynapsed chromosomes at the pachytene stage in human oocytes.
PMID 19146767·Reprod Biomed Online·2009
8-other
Reticulated platelets as a screening test to identify thrombocytopenia aetiology.
PMID 18400777·QJM·2008
8-other
ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes.
PMID 18497861·PLoS Genet·2008
7-preclinical
Pairing and synapsis in oocytes from female fetuses with euploid and aneuploid chromosome complements.
PMID 17616720·Reproduction·2007
8-other
Human fetal ovarian culture permits meiotic progression and chromosome pairing process.
PMID 16449311·Hum Reprod·2006
8-other
Novel c-KIT germline mutation in a family with gastrointestinal stromal tumors and cutaneous hyperpigmentation.
PMID 15742474·Am J Med Genet A·2005
5-case
Evolution of the meiotic prophase and of the chromosome pairing process during human fetal ovarian development.
PMID 15905292·Hum Reprod·2005
8-other
Chromosome 18 pairing behavior in human trisomic oocytes. Presence of an extra chromosome extends bouquet stage.
PMID 15855620·Reproduction·2005
8-other
De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome.
PMID 15200509·Clin Genet·2004
5-case
Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes.
PMID 15235794·Chromosoma·2004
8-other
The use of foetal ovarian stromal cell culture for cytogenetic diagnosis. Stromal ovarian culture cytogenetic diagnosis.
PMID 19002961·Cytotechnology·2003
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
- 1102 MONROE STREET
HUNTSVILLE, AL 35801 - Phone
- (256) 469-7200
Quick Facts
- NPI
- 1881847002
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 22
- Publications
- 16
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