Publications by authors named "Juan Perin"

Claim this Profile
I
Integrated digital pathology at scale: A solution for clinical diagnostics and cancer research at a large academic medical center.
Peter J Schüffler, Luke Geneslaw, D Vijay K Yarlagadda, Matthew G Hanna, Jennifer Samboy, Juan C Perin

J Am Med Inform Assoc· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clonal hematopoiesis in patients with dyskeratosis congenita.
Nieves Perdigones, Juan C Perin, Irene Schiano, Peter Nicholas, Jaclyn A Biegel

Am J Hematol· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Emergence of clonal hematopoiesis in the majority of patients with acquired aplastic anemia.
Daria V Babushok, Nieves Perdigones, Juan C Perin, Timothy S Olson, Wenda Ye

Cancer Genet· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming.
Martin Picard, Jiangwen Zhang, Saege Hancock, Olga Derbeneva, Ryan Golhar, Juan Carlos Perin

Proc Natl Acad Sci U S A· September 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Efficient digest of high-throughput sequencing data in a reproducible report.
Zhe Zhang, Jeremy Leipzig, Ariella Sasson, Angela M Yu, Juan C Perin

BMC Bioinformatics· May 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes.
Daria V Babushok, Hongbo M Xie, Jacquelyn J Roth, Nieves Perdigones, Timothy S Olson, Juan C Perin

Br J Haematol· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NMNAT1 mutations cause Leber congenital amaurosis.
Marni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, Chitra Kannabiran, Zoe Fonseca-Kelly, Juan C Perin

Nat Genet· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide analysis of interferon regulatory factor I binding in primary human monocytes.
Lihua Shi, Juan C Perin, Jeremy Leipzig, Zhe Zhang, Kathleen E Sullivan

Gene· November 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial genome sequence analysis: a custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy.
Hongbo M Xie, Juan C Perin, Theodore G Schurr, Matthew C Dulik, Sergey I Zhadanov

BMC Bioinformatics· October 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.
Tracy Busse, John M Graham, Gerald Feldman, Juan Perin, Anne Catherwood

Hum Mutat· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cytokine-induced monocyte characteristics in SLE.
Zhe Zhang, Kelly Maurer, Juan C Perin, Li Song, Kathleen E Sullivan

J Biomed Biotechnol· October 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics.
Xiaowu Gai, Juan C Perin, Kevin Murphy, Ryan O'Hara, Monica D'arcy

BMC Bioinformatics· February 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay.
Chad R Haldeman-Englert, Xiaowu Gai, Juan Carlos Perin, Melissa Ciano, Sara S Halbach

Eur J Med Genet· November 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.
Tamim H Shaikh, Xiaowu Gai, Juan C Perin, Joseph T Glessner, Hongbo Xie

Genome Res· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors.
Eric M Jackson, Angela J Sievert, Xiaowu Gai, Hakon Hakonarson, Alexander R Judkins, Juan Carlos Perin

Clin Cancer Res· March 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Systematic epitope analysis of the p26 EIAV core protein.
Adriana Soutullo, María N Santi, Juan C Perin, Leila M Beltramini, Ileana Malan Borel

J Mol Recognit· November 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Monitoring substrate and products in a bioprocess with FTIR spectroscopy coupled to artificial neural networks enhanced with a genetic-algorithm-based method for wavelength selection.
Vanina G Franco, Juan C Perín, Víctor E Mantovani, Héctor C Goicoechea

Talanta· January 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis