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Sandra S. Schneider
Sandra S. Schneider
Boston Children's Hospital
Molecular biology
Biology
Genetics
Breakpoint
Chromosomal Loss
4
Papers
285
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An 18q− Syndrome Breakpoint Resides between the Duplicated Serpins SCCA1 and SCCA2 and Arises Via a Cryptic Rearrangement With Satellite III DNA
1999
Human Molecular Genetics
Samuel G. Katz
Sandra S. Schneider
Allison J. Bartuski
Barbara J. Trask
Hillary Massa
Joan Overhauser
Marc Lalande
Peter M. Lansdorp
Gary A. Silverman
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Citations (12)
Construction and validation of yeast artificial chromosome contig maps by RecA-assisted restriction endonuclease cleavage
1998
Proceedings of the National Academy of Sciences of the United States of America
Peter Lauer
Sandra S. Schneider
Andreas Gnirke
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A serine proteinase inhibitor locus at 18q21.3 contains a tandem duplication of the human squamous cell carcinoma antigen gene.
1995
Proceedings of the National Academy of Sciences of the United States of America
Sandra S. Schneider
Charlie Schick
Kimberlee Fish
Eric Miller
Jeannette C. Pena
Sarah D. Treter
Stephanie M. Hui
Gary A. Silverman
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Citations (228)
The 18q syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.
1995
American Journal of Human Genetics
Gary A. Silverman
Sandra S. Schneider
Hillary Massa
Alan F. Flint
Marc Lalande
J C Leonard
Joan Overhauser
G van den Engh
Barbara J. Trask
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Citations (38)
1