Associate Professor of Clinical Genetics, Yale University
Medical Genetics
Dr. Allen E. Bale, MD
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Allen Bale works in the field of Medical Genetics. He went to University of Massachusetts Medical School. University of Massachusetts Medical School has a rank of 49 in research and a 12 in primary care He over the years received 5 awards: "CMS Meaningful Use Stage 1 Certification", "America's Top Doctors", "Top Doctors: New York Metro Area", "America's Top Doctors for Cancer" and "New York Magazine: Top Doctors". Allen E. Bale is a published doctor and has 101 publications published. The lastest was: 'The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.'
Publications
- Routine Genetic Testing for Thoracic Aortic Aneurysm and Dissection in a Clinical Setting.
- Alcohol intake and early-onset basal cell carcinoma in a case-control study.
- Individual exome analysis in diagnosis and management of paediatric liver failure of indeterminate aetiology.
- Novel gene identified in an exome-wide association study of tanning dependence.
- Tea, coffee, and caffeine and early-onset basal cell carcinoma in a case-control study.
- Spectrum of somatic EGFR, KRAS, BRAF, PTEN mutations and TTF-1 expression in Brazilian lung cancer patients.
- Indoor Tanning and Tanning Dependence in Young People After a Diagnosis of Basal Cell Carcinoma.
- Host Phenotype Characteristics and MC1R in Relation to Early-Onset Basal Cell Carcinoma.
- Indoor tanning and risk of early-onset basal cell carcinoma.
- Variant in the glucokinase regulatory protein (GCKR) gene is associated with fatty liver in obese children and adolescents.
- Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma.
- Functional and physical interaction between the mismatch repair and FA-BRCA pathways.
- Hereditary melanoma.
- Basal cell carcinoma arising in a nevus sebaceus in a child with facial trichoepitheliomas.
- A common variant in the patatin-like phospholipase 3 gene (PNPLA3) is associated with fatty liver disease in obese children and adolescents.
- Multiple endocrine neoplasia type 1 (MEN1) as a cancer predisposition syndrome: clues into the mechanisms of MEN1-related carcinogenesis.
- A multiplex assay for the detection and mapping of complex glycerol kinase deficiency.
- Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer.
- Multiple endocrine neoplasia type 1 interacts with forkhead transcription factor CHES1 in DNA damage response.
- PGR +331 A/G and increased risk of epithelial ovarian cancer.
- Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.
- Clinical testing for the nevoid basal cell carcinoma syndrome in a DNA diagnostic laboratory.
- Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.
- Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients.
- MEN1 tumor-suppressor protein localizes to telomeres during meiosis.
- Low frequency of recurrent BRCA1 and BRCA2 mutations in Spain.
- Hedgehog signaling and human disease.
- Prenatal diagnosis of ornithine transcarbamylase deficiency.
- DNA diagnosis with mutation-specific artificial methylation sites: application to rapid screening of delta F508.
- BRCA status, molecular markers, and clinical variables in early, conservatively managed breast cancer.
- Genetic and molecular control of folate-homocysteine metabolism in mutant mice.
- The hedgehog signalling pathway in tumorigenesis and development.
- PRAD1 (cyclin D1): a parathyroid neoplasia gene on 11q13.
- The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency.
- Report and abstracts of the First International Workshop on Chromosome 9. Held at Girton College Cambridge, UK, 22-24 March, 1992.
- Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.
- Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content.
- Incipient and overt diabetic nephropathy in African Americans with NIDDM.
- Assuming the risks: occupational disease in the years before workers' compensation.
- Medicine in the industrial battle: early workers'' compensation.
- "Hope in another direction": compensation for work-related illness among women, 1900-1960--Part I.
- "Hope in another direction": compensation for work-related illness among women, 1900-1960--Part II.
- The American compensation phenomenon.
- Can interpectoral nodes be sentinel nodes?
- Characterization of DNA adenine methylation mutants of Escherichia coli K12.
- MEN1 and FANCD2 mediate distinct mechanisms of DNA crosslink repair.
- Characterization of DNA damage-dependent cell cycle checkpoints in a menin-deficient model.
- Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin syndrome.
- Drosophila homologs of FANCD2 and FANCL function in DNA repair.
- Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused.
- Hypermutability in a Drosophila model for multiple endocrine neoplasia type 1.
- Outcome of conservatively managed early-onset breast cancer by BRCA1/2 status.
- Immunolocalization of PTCH protein in odontogenic cysts and tumors.
- Acquired and inherited basal cell carcinomas and the patched gene.
- Identification of PATCHED mutations in medulloblastomas by direct sequencing.
- PTCH gene mutations in odontogenic keratocysts.
- Sheep, lilies and human genetics.
- Treatment of a thyrotropinoma with octreotide-LAR in a patient with multiple endocrine neoplasia-1.
- The hedgehog pathway and basal cell carcinomas.
- Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman.
- Congenital linear unilateral basal cell nevus: a case report with patched gene molecular studies.
- Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the Ovarian Cancer Association Consortium pool...
- Direct molecular diagnosis of multiple endocrine neoplasia type 1.
- Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1.
- Tight linkage of the human c-erbA beta gene with the syndrome of generalized thyroid hormone resistance is present in multiple kindreds.
- PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma.
- A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5.1 centimorgans.
- Localization of a DNA segment encompassing four tRNA genes to human chromosome 14q11 and its use as an anchor locus for linkage analysis.
- Human CYP1A1 gene: cosegregation of the enzyme inducibility phenotype and an RFLP.
- A new point mutation in the 3,5,3'-triiodothyronine-binding domain of the c-erbA beta thyroid hormone receptor is tightly linked to generalized thyroid hormone resist...
- Relationship between head circumference and height in normal adults and in the nevoid basal cell carcinoma syndrome and neurofibromatosis type I.
- A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12.
- Two RFLPs at the glutathione S-transferase 3 gene.
- Ornithine transcarbamylase polymorphism detected by PCR introduction of DraI site.
- Localization of CYP2F1 by multipoint linkage analysis and pulsed-field gel electrophoresis.
- Allelic loss from chromosome 11 in parathyroid tumors.
- Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19.
- Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22.
- A base mutation of the C-erbA beta thyroid hormone receptor in a kindred with generalized thyroid hormone resistance. Molecular heterogeneity in two other kindreds.
- Analysis of gonadotropin-releasing hormone gene structure in families with familial central precocious puberty and idiopathic hypogonadotropic hypogonadism.
- Genetic abnormalities in sporadic parathyroid adenomas.
- Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndrome.
- Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11.
- Six RFLPs for human T cell receptor alpha (TCRA) on chromosome 14.
- Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1.
- Familial Sotos syndrome (cerebral gigantism): craniofacial and psychological characteristics.
- A retinoic acid receptor cDNA probe (RAR2) identifies a moderately frequent RFLP on chromosome 17.
- A cDNA probe (PheA12) from the hc-(ERBA) gene on chromosome 3 detects a high frequency RFLP.
- Tight linkage between the syndrome of generalized thyroid hormone resistance and the human c-erbA beta gene.
- Internal malignancy in genetic hemochromatosis.
- Linkage relationships among four 11p markers in the Utah dataset.
- Linkage analysis in spinopontine atrophy: correlation of HLA linkage with phenotypic findings in hereditary ataxia.
- Linkage between the genes for Wolfram syndrome and brachydactyly E.
- CEPH consortium map of chromosome 14.
- Localization of the gene for the nevoid basal cell carcinoma syndrome.
- Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland.
- Molecular mechanisms of neoplasia in multiple endocrine neoplasia type 1-related and sporadic tumors of the pancreatic islet cells.
- Prenatal diagnosis of Gorlin syndrome.
- Nevoid basal cell carcinoma syndrome.
- Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q.
Schools
University of Massachusetts Worcester Campus
Doctors Specialties
- Clinical Genetics
- Clinical Molecular Genetics
- Internal Medicine
- Medical Genetics
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
- America's Top Doctors
- Top Doctors: New York Metro Area
- America's Top Doctors for Cancer
- New York Magazine: Top Doctors
Education
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Allegheny General Hospital - Western Pennsylvania Hospital -
University of Massachusetts Medical School
Hospital
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Yale-New Haven Hospital
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1992795371 |
| Last Name Of The Provider | BALE |
| First Name Of The Provider | ALLEN |
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