Corinne D. Boehm
Baylor College of Medicine(US)
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Parvovirus B19 Infection Studies
Most-Cited Works
- → Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster(1982)933 cited
- → The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities(2015)685 cited
- → Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia(2000)469 cited
- → Nonrandom association of polymorphic restriction sites in the β-globin gene cluster(1982)402 cited
- → ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations(2001)319 cited
- → Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes(1988)293 cited
- → A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion(1994)234 cited
- → Insights into genetics, human biology and disease gleaned from family based genomic studies(2019)211 cited
- → New Tools for Mendelian Disease Gene Identification: PhenoDB Variant Analysis Module; and GeneMatcher, a Web-Based Tool for Linking Investigators with an Interest in the Same Gene(2015)180 cited
- → Improved Detection of the Sickle Mutation by DNA Analysis(1982)175 cited