Human structural variation: mechanisms of chromosome rearrangements

Por Weckselblatt, Brooke, Rudd, M. Katharine
Publicado no Trends Genet (2015)

Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis

Por Weckselblatt, Brooke, Hermetz, Karen E., Rudd, M. Katharine
Publicado no Genome Res (2015)

The evolutionary dynamics of α-satellite

Por Rudd, M. Katharine, Wray, Gregory A., Willard, Huntington F.
Publicado em 2006

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

Por Newman, Scott, Hermetz, Karen E., Weckselblatt, Brooke, Rudd, M. Katharine
Publicado no Am J Hum Genet (2015)

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

Por Rudd, M. Katharine, Mays, Robert W., Schwartz, Stuart, Willard, Huntington F.
Publicado em 2003

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

Por Hermetz, Karen E, Surti, Urvashi, Cody, Jannine D, Rudd, M Katharine
Publicado em 2012

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

Por Bose, Promita, Hermetz, Karen E., Conneely, Karen N., Rudd, M. Katharine
Publicado em 2014

Assembly and characterization of heterochromatin and euchromatin on human artificial chromosomes

Por Grimes, Brenda R, Babcock, Jennifer, Rudd, M Katharine, Chadwick, Brian, Willard, Huntington F
Publicado em 2004

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

Por Lam, Ai Leen, Boivin, Christopher D., Bonney, Caitlin F., Rudd, M. Katharine, Sullivan, Beth A.
Publicado em 2006

Elevated Rates of Sister Chromatid Exchange at Chromosome Ends

Por Rudd, M. Katharine, Friedman, Cynthia, Parghi, Sean S, Linardopoulou, Elena V, Hsu, Li, Trask, Barbara J
Publicado em 2007

Sequences Associated with Centromere Competency in the Human Genome

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

GNB3 overexpression causes obesity and metabolic syndrome

Por Ozdemir, Alev Cagla, Wynn, Grace M., Vester, Aimee, Weitzmann, M. Neale, Neigh, Gretchen N., Srinivasan, Shanthi, Rudd, M. Katharine
Publicado no PLoS One (2017)

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

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

Segmental duplications mediate novel, clinically relevant chromosome rearrangements

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

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

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

Terminal 18q deletions are stabilized by neotelomeres

Por 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
Publicado no Mol Cytogenet (2015)

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

Por 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.
Publicado em 2009

Large Contiguous Gene Deletions in Sjögren-Larsson Syndrome

Por 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.
Publicado em 2011

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

Por 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
Publicado em 2010

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements

Por 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
Publicado em 2011