Human structural variation: mechanisms of chromosome rearrangements

by Weckselblatt, Brooke, Rudd, M. Katharine
Published in Trends Genet (2015)

Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis

by Weckselblatt, Brooke, Hermetz, Karen E., Rudd, M. Katharine
Published in Genome Res (2015)

The evolutionary dynamics of α-satellite

by Rudd, M. Katharine, Wray, Gregory A., Willard, Huntington F.
Published 2006

Next-Generation Sequencing of Duplication CNVs Reveals that Most Are Tandem and Some Create Fusion Genes at Breakpoints

by Newman, Scott, Hermetz, Karen E., Weckselblatt, Brooke, Rudd, M. Katharine
Published in Am J Hum Genet (2015)

Human Artificial Chromosomes with Alpha Satellite-Based De Novo Centromeres Show Increased Frequency of Nondisjunction and Anaphase Lag

by Rudd, M. Katharine, Mays, Robert W., Schwartz, Stuart, Willard, Huntington F.
Published 2003

A recurrent translocation is mediated by homologous recombination between HERV-H elements

by Hermetz, Karen E, Surti, Urvashi, Cody, Jannine D, Rudd, M Katharine
Published 2012

Tandem Repeats and G-Rich Sequences Are Enriched at Human CNV Breakpoints

by Bose, Promita, Hermetz, Karen E., Conneely, Karen N., Rudd, M. Katharine
Published 2014

Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes

by Grimes, Brenda R, Babcock, Jennifer, Rudd, M Katharine, Chadwick, Brian, Willard, Huntington F
Published 2004

Human centromeric chromatin is a dynamic chromosomal domain that can spread over noncentromeric DNA

by Lam, Ai Leen, Boivin, Christopher D., Bonney, Caitlin F., Rudd, M. Katharine, Sullivan, Beth A.
Published 2006

Elevated Rates of Sister Chromatid Exchange at Chromosome Ends

by Rudd, M. Katharine, Friedman, Cynthia, Parghi, Sean S, Linardopoulou, Elena V, Hsu, Li, Trask, Barbara J
Published 2007

Sequences Associated with Centromere Competency in the Human Genome

by Hayden, Karen E., Strome, Erin D., Merrett, Stephanie L., Lee, Hye-Ran, Rudd, M. Katharine, Willard, Huntington F.
Published 2013

GNB3 overexpression causes obesity and metabolic syndrome

by Ozdemir, Alev Cagla, Wynn, Grace M., Vester, Aimee, Weitzmann, M. Neale, Neigh, Gretchen N., Srinivasan, Shanthi, Rudd, M. Katharine
Published in PLoS One (2017)

A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband

by Wilson, Nicole K. A., Lee, Yohan, Long, Robert, Hermetz, Karen, Rudd, M. Katharine, Miller, Rachel, Rapoport, Judith L., Addington, Anjené M.
Published 2011

Segmental duplications mediate novel, clinically relevant chromosome rearrangements

by Rudd, M. Katharine, Keene, Julia, Bunke, Brian, Kaminsky, Erin B., Adam, Margaret P., Mulle, Jennifer G., Ledbetter, David H., Martin, Christa L.
Published 2009

Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism

by Hermetz, Karen E., Newman, Scott, Conneely, Karen N., Martin, Christa L., Ballif, Blake C., Shaffer, Lisa G., Cody, Jannine D., Rudd, M. Katharine
Published 2014

Terminal 18q deletions are stabilized by neotelomeres

by Guilherme, Roberta Santos, Hermetz, Karen E, Varela, Patrícia Teixeira, Perez, Ana Beatriz Alvarez, Meloni, Vera Ayres, Rudd, M Katharine, Kulikowski, Leslie Domenici, Melaragno, Maria Isabel
Published in Mol Cytogenet (2015)

Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event

by Rudd, M. Katharine, Endicott, RaeLynn M., Friedman, Cynthia, Walker, Megan, Young, Janet M., Osoegawa, Kazutoyo, de Jong, Pieter J., Green, Eric D., Trask, Barbara J.
Published 2009

Large Contiguous Gene Deletions in Sjögren-Larsson Syndrome

by Engelstad, Holly, Carney, Gael, S'Aulis, Dana, Rise, Janae, Sanger, Warren G., Rudd, M. Katharine, Richard, Gabriele, Carr, Christopher W., Abdul-Rahman, Omar A., Rizzo, William B.
Published 2011

Development of genomic resources for the prairie vole (Microtus ochrogaster): construction of a BAC library and vole-mouse comparative cytogenetic map

by McGraw, Lisa A, Davis, Jamie K, Lowman, Josh J, ten Hallers, Boudewijn FH, Koriabine, Maxim, Young, Larry J, de Jong, Pieter J, Rudd, M Katharine, Thomas, James W
Published 2010

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements

by Luo, Yue, Hermetz, Karen E., Jackson, Jodi M., Mulle, Jennifer G., Dodd, Anne, Tsuchiya, Karen D., Ballif, Blake C., Shaffer, Lisa G., Cody, Jannine D., Ledbetter, David H., Martin, Christa L., Rudd, M. Katharine
Published 2011