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Human Structural Variation: Mechanisms of Chromosome Rearrangements di Brooke Weckselblatt, M. Katharine Rudd

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Paired-Duplication Signatures Mark Cryptic Inversions and Other Complex Structural Variation di Harrison Brand, Ryan L. Collins, Carrie Hanscom, Jill A. Rosenfeld, Vamsee Pillalamarri, Matthew R. Stone, Fontina Kelley, Tamara Mason, Lauren Margolin, Stacey Eggert, Elyse Mitchell, Jennelle C. Hodge, James F. Gusella, Stephan Sanders, Michael E. Talkowski

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Comparing genomes with rearrangements and segmental duplications di Mingfu Shao, Bernard M. E. Moret

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Genome-Wide Study of Structural Variants in Bovine Holstein, Montbéliarde and Normande Dairy Breeds di Mekki Boussaha, Diane Esquerré, Johanna Barbieri, Anis Djari, Alain Pinton, Rabia Letaïef, Gérald Salin, Fréderic Escudié, Alain Roulet, Sébastien Fritz, Franck Samson, Cécile Grohs, Maria Bernard, Christophe Klopp, Didier Boichard, Dominique Rocha

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Analysis of the DNA sequence and duplication history of human chromosome 15 di Michael C. Zody, Manuel Garber, Ted Sharpe, Sarah Young, Lee Rowen, Keith O'Neill, Charles A. Whittaker, Michael Kamal, Jean L. Chang, Christina A. Cuomo, Ken Dewar, Michael G. FitzGerald, Chinnappa D. Kodira, Anup Madan, Shizhen Qin, Xiaoping Yang, Nissa Abbasi, Amr Abouelleil, Harindra Arachchi, Lida Baradarani, Brian Birditt, Scott Bloom, Toby Bloom, Mark L. Borowsky, Jeremy Burke, Jonathan A. Butler, April Cook, Kurt DeArellano, David DeCaprio, Lester Dorris, Monica Dors, Evan E. Eichler, Reinhard Engels, Jessica Fahey, Peter Fleetwood, Cynthia Friedman, Gary Gearin, Jennifer L. Hall, Grace Hensley, Ericka M. Johnson, C. Jones, Asha Kamat, Amardeep Kaur, Devin P. Locke, Anuradha Madan, Glen Munson, David B. Jaffe, Annie Lui, Pendexter Macdonald, Evan Mauceli, Jerome W. Naylor, Ryan Nesbitt, Robert Nicol, Sinéad B. O'Leary, Amber Ratcliffe, Steven D. Rounsley, Xinwei She, Katherine Sneddon, Sandra Stewart, Carrie Sougnez, Sabrina M. Stone, Kerri Topham, Dascena Vincent, Shunguang Wang, Andrew Zimmer, Bruce W. Birren, Leroy Hood, Eric S. Lander, Chad Nusbaum

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Molecular pathology of schizophrenia: more than one disease process? di T.J. Crow

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Duplication and Gene Conversion in the Drosophila melanogaster Genome di Naoki Osada, Hideki Innan

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Tandem Repeats and G-Rich Sequences Are Enriched at Human CNV Breakpoints di Promita Bose, Karen Hermetz, Karen N. Conneely, M. Katharine Rudd

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Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification di Renqian Du, Chuncheng Lu, Zhengwen Jiang, Shilin Li, Ruixiao Ma, Haijia An, Miaofei Xu, Yu An, Yankai Xia, Jin Li, Xinru Wang, Feng Zhang

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The reference human nuclear mitochondrial sequences compilation validated and implemented on the UCSC genome browser di Domenico Simone, Francesco Maria Calabrese, Martin Lang, Giuseppe Gasparre, Marcella Attimonelli

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The genomic basis of the Williams – Beuren syndrome di Cornelia Schubert

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Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia di Jean‐Marc Aury, Olivier Jaillon, Laurent Duret, Benjamin Noël, Claire Jubin, Betina M. Porcel, Béatrice Segurens, Vincent Daubin, Véronique Anthouard, Nathalie Aiach, Olivier Arnaiz, Alain Billaut, Janine Beisson, Isabelle Blanc, Khaled Bouhouche, Francisco Câmara, Sandra Duharcourt, Roderic Guigó, Delphine Gogendeau, Michaël Katinka, Anne‐Marie Keller, Roland Kissmehl, Catherine Klotz, France Koll, Anne Le Mouël, Gersende Lepère, Sophie Malinsky, Mariusz Nowacki, J Nowak, Helmut Plattner, Julie Poulain, Françoise Ruiz, Vincent Serrano, Marek Zagulski, Philippe Dessen, Mireille Bétermier, Jean Weissenbach, Claude Scarpelli, Vincent Schächter, Linda Sperling, Éric Meyer, Jean Cohen, Patrick Wincker

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The Mosaic Structure of Human Pericentromeric DNA: A Strategy for Characterizing Complex Regions of the Human Genome di Juliann E. Horvath, Stuart Schwartz, Evan E. Eichler

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Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons di Miguel Angel Pujana, Marga Nadal, Míriam Guitart, Lluı́s Armengol, Mónica Gratacòs, Xavier Estivill

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Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements di Lluı́s Armengol

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Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity di Ruxandra Bachmann‐Gagescu, Heather C. Mefford, Charles A. Cowan, Gwen M. Glew, Anne Hing, Stephanie E Wallace, Patricia I. Bader, Aline I. Hamati, Pamela J. Reitnauer, Rosemarie Smith, David W. Stockton, Hiltrud Muhle, Ingo Helbig, Evan E. Eichler, Blake C. Ballif, Jill A. Rosenfeld, Karen D. Tsuchiya

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Evolution and functional divergence of NLRPgenes in mammalian reproductive systems di Xin Tian, Géraldine Pascal, Philippe Monget

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Heterogeneous Duplications in Patients with Pelizaeus-Merzbacher Disease Suggest a Mechanism of Coupled Homologous and Nonhomologous Recombination di Karen Woodward, Maria Cundall, Karen Sperle, Erik A. Sistermans, Mark T. Ross, Gareth R. Howell, Susan Gribble, D. C. Burford, Nigel P. Carter, Donald L. Hobson, James Garbern, John Kamholz, Henry H.Q. Heng, M. E. Hodes, Sue Malcolm, Grace M. Hobson

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Human-Specific Duplication and Mosaic Transcripts: The Recent Paralogous Structure of Chromosome 22 di Jeffrey A. Bailey, Amy M. Yavor, Luigi Viggiano, Doriana Misceo, Juliann E. Horvath, Nicoletta Archidiacono, Stuart Schwartz, Mariano Rocchi, Evan E. Eichler

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Structural diversity and African origin of the 17q21.31 inversion polymorphism di Karyn Meltz Steinberg, Francesca Antonacci, Peter H. Sudmant, Jeffrey M. Kidd, Colin Campbell, Laura Vives, Maika Malig, Laura Scheinfeldt, William Beggs, Muntaser E. Ibrahim, Godfrey Lema, Thomas Nyambo, Sabah A. Omar, Jean-Marie Bodo, Alain Froment, Michael P. Donnelly, Kenneth K. Kídd, Sarah A. Tishkoff, Evan E. Eichler

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