Professor, Medical and Molecular Genetics, Indiana University School of Medicine
Medical Genetics
Dr. Gail H. VanCe, MD
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Gail VanCe works in the field of Medical Genetics. Gail VanCe is also published. She has 96 publications published. The lastest publication: "De novo 10q22 interstitial deletion.'
Publications
- Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199.
- Report of New Haplotype for ABCC2 Gene: rs17222723 and rs8187718 in cis.
- Reply to E.A. Rakha et al.
- Cyclophosphamide/fludarabine nonmyeloablative allotransplant for acute myeloid leukemia.
- Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine.
- Luminal subtypes predict improved survival following central nervous system metastasis in patients with surgically managed metastatic breast carcinoma.
- Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: american society of clinical oncology/college of american pathologists clinical ...
- Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis.
- Fluorescence In Situ Hybridization (FISH) as an Aid for the Diagnosis of Graft-Versus-Host Disease in Two Multivisceral Organ Transplant Patients.
- Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism.
- Prognostic and Predictive Value of Tumor Vascular Endothelial Growth Factor Gene Amplification in Metastatic Breast Cancer Treated with Paclitaxel with and without Bev...
- Establishment and characterization of a novel cell line derived from human thymoma AB tumor.
- Cancer-associated alteration of pericentromeric heterochromatin may contribute to chromosome instability.
- Duplication of 18q21.32-q22.3 identified in a stillborn and two relatives with minimal dysmorphic features.
- Glioblastoma occurring at the site of a previous medulloblastoma following a 5-year remission period.
- College of american pathologists proposal for the oversight of laboratory-developed tests.
- Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia.
- Most primary central nervous system diffuse large B-cell lymphomas occurring in immunocompetent individuals belong to the nongerminal center subtype: a retrospective a...
- Genital anomalies in three male siblings with Simpson-Golabi-Behmel syndrome.
- Interphase FISH demonstrates that human adipose stromal cells maintain a high level of genomic stability in long-term culture.
- Phenotypic variability in trisomy 13 mosaicism: two new patients and literature review.
- A case of de novo partial tetrasomy of distal 6p and review of the literature.
- Chronic myelomonocytic leukemia: The role of bone marrow biopsy immunohistology.
- A report of three patients with an interstitial deletion of chromosome 15q24.
- Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic tris...
- AML1-FOG2 fusion protein in myelodysplasia.
- Acute panmyelosis with myelofibrosis: an entity distinct from acute megakaryoblastic leukemia.
- Partial trisomy 2q: report of a patient with dup (2)(q33.1q35).
- Chronic lymphocytic leukemia/small lymphocytic lymphoma with trisomy 12 and focal cyclin d1 expression: a potential diagnostic pitfall.
- Characterization of gains, losses, and regional amplification in testicular germ cell tumor cell lines by comparative genomic hybridization.
- Turner syndrome (45x) with clitoromegaly.
- Update on late relapse of germ cell tumor: a clinical and molecular analysis.
- Acute graft-versus-host disease of the lung after liver transplantation.
- Therapy-related myeloid neoplasm with bone marrow involvement, myelosarcoma, and a t(8;16)(p11.2;p13.3)-a case report.
- Molecular Genetic Tests for FLT3, NPM1, and CEBPA in Acute Myeloid Leukemia.
- Detection of recurrent cytogenetic abnormalities in acute lymphoblastic and myeloid leukemias using fluorescence in situ hybridization.
- Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.
- Detection of house-dust-mite allergen in amniotic fluid and umbilical-cord blood.
- Variable phenotype of familial adenomatous polyposis in pedigrees with 3'' mutation in the APC gene.
- Costimulatory molecules in the developing human gastrointestinal tract: a pathway for fetal allergen priming.
- Exposure of the fetus and infant to hens'' egg ovalbumin via the placenta and breast milk in relation to maternal intake of dietary egg.
- Ovalbumin-specific immunoglobulin G and subclass responses through the first 5 years of life in relation to duration of egg sensitization and the development of asthma.
- Ocular manifestations of Hansen''s disease.
- Serum ovalbumin-specific immunoglobulin G responses during pregnancy reflect maternal intake of dietary egg and relate to the development of allergy in early infancy.
- Toward quality assurance for metaphase FISH: a multi-center experience.
- Testing for BRCA1 in hereditary breast cancer.
- Modification of T-cell receptor Vbeta repertoire in response to allergen stimulation in peanut allergy.
- Toward quality assurance for metaphase FISH: a multicenter experience.
- Cytogenetics: a short review and update.
- Partners with reciprocal translocations: genetic counseling for the ''double translocation''.
- The ACMG CYTO2000 subcommittee?
- The human A1 adenosine receptor: ligand binding properties, sites of somatic expression and chromosomal localization.
- Multiplex PCR: critical parameters and step-by-step protocol.
- Potential role of hematopoietic stem cell transplantation in children with secondary acute lymphocytic leukemia.
- Extensive analysis of mosaicism in a case of Turner syndrome: the experience of 287 cytogenetic laboratories. College of American Pathologists/American College of Medi...
- A 37-year-old man with a pleural mass.
- Cytogenetic findings of a child with transcobalamin II deficiency.
- Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.
- Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
- Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies.
- Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.
- Genetic diagnosis of PLP gene duplications/deletions in patients with Pelizaeus-Merzbacher disease.
- Long-term disease-free survival after nonmyeloablative cyclophosphamide/fludarabine conditioning and related/unrelated allotransplantation for acute myeloid leukemia/m...
- 49,XXXXY: a distinct phenotype. Three new cases and review.
- Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing.
- HER-2/neu expression in germ cell tumours.
- A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes.
- The embryonic stem cell transcription factors Oct-4 and FoxD3 interact to regulate endodermal-specific promoter expression.
- Cytogenetic analysis and construction of a BAC contig across a common neocentromeric region from 9p.
- Urorectal septum malformation sequence: report of thirteen additional cases and review of the literature.
- A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.
- Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.
- Small marker chromosome identification in metaphase and interphase using centromeric multiplex fish (CM-FISH).
- Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implications.
- Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia.
- Mild "duplication 6q syndrome": a case with partial trisomy (6)(q23.3q25.3).
- An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences.
- De novo 10q22 interstitial deletion.
- Triple-color FISH analysis of 12p amplification in testicular germ-cell tumors using 12p band-specific painting probes.
- Secondary leukemias in refractory germ cell tumor patients undergoing autologous stem-cell transplantation using high-dose etoposide.
- Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature.
- Characterization of multiple 12p rearrangements in testicular germ cell tumor cell line 833K and its subclone 64CP by chromosome microdissection.
- Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients.
- Proficiency testing for laboratories performing fluorescence in situ hybridization with chromosome-specific DNA probes.
- Problems with ISCN FISH Nomenclature make it not practical for use in clinical test reports or cytogenetic databases [corrected].
- Evaluating current policy for detecting mosaicism in amniotic fluid cultures: implications for current cell counting practices.
- Large cell carcinoma of the lung mimicking a germ cell tumor: the potential value of chromosome analysis.
- Cytogenetic heteromorphisms: survey results and reporting practices of giemsa-band regions that we have pondered for years.
- Clinical laboratory reports in molecular pathology.
- Detection of clonal IGH gene rearrangements: summary of molecular oncology surveys of the College of American Pathologists.
- Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research C...
- American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer.
- Genetic heterogeneity in HER2 testing in breast cancer: panel summary and guidelines.
- Referral patterns of Indiana oncologists for colorectal cancer genetic services.
- Utility of interphase FISH to stratify patients into cytogenetic risk categories at diagnosis of AML in an Eastern Cooperative Oncology Group (ECOG) clinical trial (E1...
Schools
Michigan State University
Wm Beaumont
University Of Minnesota
Doctors Specialties
- Clinical Cytogenetics
- Clinical Genetics
- Clinical Pathology
- Pediatrics
- Medical Genetics
Accepted Insurances
Education
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University of Minnesota at Fairview -
William Beaumont Hospital -
Michigan State University College of Human Medicine
Hospital
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IU Health Methodist Hospital -
Riley Hospital for Children at Indiana University Health
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1649236217 |
| Last Name Of The Provider | VANCE |
| First Name Of The Provider | GAIL |
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