A. Itsara

发表

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.

C. Baker, N. de Leeuw, M. Fichera, 2008, The New England journal of medicine.

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Avni Santani, Steven Joffe, Michael J Bamshad, 2015, Genome research.

Low Energy Quantum Scattering in Waveguides

A. Itsara, 2005 .

Hall of mirrors scattering from an impurity in a quantum wire

E. Heller, A. Itsara, J. Vaishnav, 2005, quant-ph/0511137.

A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

Deborah L. Levy, Gregory M. Cooper, Brian L. Browning, 2010, Nature Genetics.

De novo rates and selection of large copy number variation.

Deborah A Nickerson, Isabelle Romieu, Evan E Eichler, 2010, Genome research.

Population analysis of large copy number variants and hotspots of human genetic disease.

Richard M Myers, Deborah A Nickerson, Jun Li, 2009, American journal of human genetics.

Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.

C. Baker, E. Eichler, T. Graves, 2012, American journal of human genetics.

Resolving genomic disorder–associated breakpoints within segmental DNA duplications using massively parallel sequencing

J. Shendure, E. Eichler, A. Itsara, 2014, Nature Protocols.

Optimal design of oligonucleotide microarrays for measurement of DNA copy-number.

E. Eichler, S. Schwartz, C. Alkan, 2007, Human molecular genetics.

A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration

Rajiv Raman, Ronnie George, Lingam Vijaya, 2011, PloS one.

De novo rates and selection of large copy number variation.

E. Eichler, D. Nickerson, Joshua D. Smith, 2010, Genome research.