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Bernice A. Allitto

Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens
2011 · Elaine A Sugarman, Narasimhan Nagan, et al. · European Journal of Human Genetics · 664
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Differences in SMN1 allele frequencies among ethnic groups within North America
2009 · B C Hendrickson, C Donohoe, et al. · Journal of Medical Genetics · 172
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The Huntington's disease candidate region exhibits many different haplotypes
1992 · Marcy E. MacDonald, Andrea Novelletto, et al. · Nature Genetics · 154
Standards and Guidelines for CFTR Mutation Testing
2002 · Carolyn Sue Richards, Linda A. Bradley, et al. · Genetics in Medicine · 130
A DNA Segment Encoding Two Genes Very Tightly Linked to Huntington's Disease
1987 · T. Conrad Gilliam, Maja Bucan, et al. · Science · 109
Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel
2001 · Ruth A Heim, Elaine A Sugarman, et al. · Genetics in Medicine · 97
Recombination events suggest potential sites for the Huntington's disease gene
1989 · Marcy E. MacDonald, Jonathan L. Haines, et al. · Neuron · 91
The I148T CFTR allele occurs on multiple haplotypes: A complex allele is associated with cystic fibrosis
2002 · Elizabeth M. Rohlfs, Zhaoqing Zhou, et al. · Genetics in Medicine · 83
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Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation
1990 · M. Bućan, M. Zimmer, et al. · Genomics · 82
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CFTR mutation distribution among U.S. Hispanic and African American individuals: Evaluation in cystic fibrosis patient and carrier screening populations
2004 · Elaine A. Sugarman, Elizabeth M. Rohlfs, et al. · Genetics in Medicine · 80
Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population
2011 · Elizabeth M Rohlfs, Zhaoqing Zhou, et al. · Clinical Chemistry · 75
Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina
2003 · Lorna S. Timmreck, Mark R. Gray, et al. · American Journal of Medical Genetics Part A · 63
A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.
1990 · G P Bates, M E MacDonald, et al. · PubMed · 62
Clustering of multiallele DNA markers near the Huntington's disease gene.
1989 · M E MacDonald, S V Cheng, et al. · Journal of Clinical Investigation · 53
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Increased recombination adjacent to the Huntington disease-linked D4S10 marker
1991 · Bernice A. Allitto, Marcy E. MacDonald, et al. · Genomics · 51
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Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
1994 · L M Brzustowicz, B A Allitto, et al. · PubMed Central · 46
Mapping of cosmid clones in Huntington's disease region of chromosome 4
1991 · William L. Whaley, Gillian P. Bates, et al. · Somatic Cell and Molecular Genetics · 46
Micronucleus-specific DNA sequences in an amicronucleate mutant of Tetrahymena
1984 · Kathleen Karrer, Susan Stein-Gavens, et al. · Developmental Biology · 34
High Allelic Heterogeneity Between Afro-Brazilians and Euro-Brazilians Impacts Cystic Fibrosis Genetic Testing
2003 · Salmo Raskin, Lilian Pereira, et al. · Genetic Testing · 24
Detection by PCR of the VNTR polymorphism at D4S95
1991 · Bernice A. Allitto, Glenn T. Horn, et al. · Nucleic Acids Research · 14
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A family of DNA sequences is reproducibly rearranged in the somatic nucleus ofTetrahymena
1986 · Bernice A. Allitto, Kathleen M. Karrer · Nucleic Acids Research · 10
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4
1992 · B.A. Allitto, A.I. McClatchey, et al. · Molecular and Cellular Probes · 6
Fetal echogenic bowel and a dilated loop of bowel associated with cystic fibrosis (CF mutations ΔF508 and 2183AA→G
1998 · Peggy W. Rush, Subodh Vats, et al. · Prenatal Diagnosis · 4
Quantitation of immunoglobulins in the effusions of human ovarian epithelial neoplasms
1984 · William H. Kutteh, Stanley A. Gall, et al. · American Journal of Obstetrics and Gynecology · 4
Commentary on “The 1604A (R496H) mutation in Gaucher disease: genotype/phenotype correlation,” by Brautbar et al.
2003 · Bernice A. Allitto, Elaine A. Sugarman · Blood Cells Molecules and Diseases · 1
Works count: 30
Citation count: 2,156
H-index: 19
I10-index: 21
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