Samuel A. Latt

Boston Children's Hospital — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

45h-index8.5kcitations92works0.02yr avg
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Research Topics

DNA and Nucleic Acid Chemistry(33), DNA Repair Mechanisms(28), Genomic variations and chromosomal abnormalities(17), Carcinogens and Genotoxicity Assessment(16), Chromosomal and Genetic Variations(13)

Publications92 total

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader‐Willi syndrome
American Journal of Medical Genetics·1989· 75 cited
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndrome
American Journal of Medical Genetics·1989· 157 cited
Identification of ataxia telangiectasia heterozygotes by flow cytometric analysis of X-ray damage
Mutation research. Fundamental and molecular mechanisms of mutagenesis·1989· 17 cited
Flow cytometric analysis of X-ray sensitivity in ataxia telangiectasia
Mutation research. Fundamental and molecular mechanisms of mutagenesis·1989· 68 cited
Analysis of peripheral maternal blood samples for the presence of placenta‐derived cells using Y‐specific probes and McAb H315
Prenatal Diagnosis·1988· 53 cited
Reply to F. Greenberg and D.H. Ledbetter: “Chromosome abnormalities and Williams syndrome”
American Journal of Medical Genetics·1988
Y-Specific DNA Sequences in Male Patients with 46, XX and 47, XXX Karyotypes
Obstetrical & Gynecological Survey·1988
Y-Specific DNA Sequences in Male Patients with 46, XX and 47, XXX Karyotypes
Obstetrical & Gynecological Survey·1988
The Amyloid β Protein Gene Is Not Duplicated in Brains from Patients with Alzheimer's Disease
Science·1987· 139 cited
Y‐specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes
American Journal of Medical Genetics·1987· 21 cited
Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p
Human Genetics·1987· 29 cited
Clinical heterogeneity associated with deletions in the long arm of chromosome 15: Report of 3 new cases and their possible genetic significance
American Journal of Medical Genetics·1987· 171 cited
Amplification of IMR-32 clones 8, G21, and N-myc in human neuroblastoma xenografts.
PubMed·1987· 20 cited
Direct hybridization to DNA from small numbers of flow‐sorted nucleated newborn cells
Cytometry·1987· 6 citedOpen Access
Y-190, a DNA probe for the sensitive detection of Y-derived marker chromosomes and mosaicism
Human Genetics·1987· 47 cited
Rapid cloning of multiple amplified nucleotide sequences from human neuroblastoma cell lines by phenol emulsion competitive DNA reassociation
Gene·1987· 19 cited
Mapping by chromosome sorting of several gene probes, including C‐myc, to the derivative chromosomes of a 3;8 translocation associated with familial renal cancer
Cytometry·1986· 24 citedOpen Access
Amplification and rearrangement of DNA sequences from the chromosomal region 2p24 in human neuroblastomas.
PubMed·1986· 47 cited
Construction, analysis, and application to 46,XY gonadal dysgenesis of a recombinant phage DNA library from flow‐sorted human Y chromosomes
Cytometry·1986· 17 cited
Use of Y chromosome specific probes to detect low level sex chromosome mosaicism
Clinical Genetics·1986· 13 cited
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Frequent Co-authors

Marc Lalande(7), Rhona Schreck(4), James W. Allen(4), Timothy A. Donlon(4), Umadevi Tantravahi(4), Robert H. Wharton(3), Herbert A. Sober(3), Elhanan Sahar(3), Nancy E. Kohl(2), Naotoshi Kanda(2), G.A.P. Bruns(2), Frederick W. Alt(2), Randal J. Kaufman(2), Kenneth S. Loveday(2), Charlotte P. Dougherty(2), Charles F. Shuler(2), Louis M. Kunkel(2), M. Eisenhard(2), Bert L. Vallée(2), Lawrence C. Kaplan(2)