Genome-scale portrait and evolutionary significance of human-specific core promoter tri- and tetranucleotide short tandem repeats

by N. Nazaripanah, F. Adelirad, A. Delbari, R. Sahaf, T. Abbasi-Asl, M. Ohadi
Published 2018-04-01

Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure

by Madeleine J. Murtagh, Mwenza T. Blell, Olly W. Butters, Lorraine Cowley, Edward S. Dove, Alissa Goodman, Rebecca L. Griggs, Alison Hall, Nina Hallowell, Meena Kumari, Massimo Mangino, Barbara Maughan, Melinda C. Mills, Joel T. Minion, Tom Murphy, Gillian Prior, Matthew Suderman, Susan M. Ring, Nina T. Rogers, Stephanie J. Roberts, Catherine Van der Straeten, Will Viney, Deborah Wiltshire, Andrew Wong, Neil Walker, Paul R. Burton
Published 2018-04-01

TRPM3_miR-204: a complex locus for eye development and disease

by Alan Shiels
Published 2020-02-01

Editorial

by Jin Li, Goldstein David B
Published 2003-11-01

A survey of data mining methods for linkage disequilibrium mapping

by Onkamo Päivi, Toivonen Hannu
Published 2006-03-01

State of the art <it>de novo </it>assembly of human genomes from massively parallel sequencing data

by Li Yingrui, Hu Yujie, Bolund Lars, Wang Jun
Published 2010-04-01

Genome-wide analysis of the human <it>Alu </it>Yb-lineage

by Carter Anthony B, Salem Abdel-Halim, Hedges Dale J, Keegan Catherine, Kimball Beth, Walker Jerilyn A, Watkins W, Jorde Lynn B, Batzer Mark A
Published 2004-03-01

Changes in <it>Human Genomics</it>

by Vasiliou Vasilis
Published 2011-01-01

Oxidative stress-induced chromosome breaks within the ABL gene: a model for chromosome rearrangement in nasopharyngeal carcinoma

by Sang-Nee Tan, Sai-Peng Sim, Alan Soo-Beng Khoo
Published 2018-06-01

A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa

by Yabin Chen, Li Huang, Xiaodong Jiao, Sheikh Riazuddin, S. Amer Riazuddin, J. Fielding Hetmancik
Published 2018-07-01

A new bioinformatics tool to help assess the significance of BRCA1 variants

by Isabelle Cusin, Daniel Teixeira, Monique Zahn-Zabal, Valentine Rech de Laval, Anne Gleizes, Valeria Viassolo, Pierre O. Chappuis, Pierre Hutter, Amos Bairoch, Pascale Gaudet
Published 2018-07-01

Visionary genomics

by Petrash J, Ruzycki Philip A, Zablocki Gregory J
Published 2011-10-01

Gene family matters: expanding the HGNC resource

by Daugherty Louise C, Seal Ruth L, Wright Mathew W, Bruford Elspeth A
Published 2012-07-01

Chromosomal phenotypes and submicroscopic abnormalities

by Devriendt Koen, Vermeesch Joris R
Published 2004-01-01

<it>In-silico </it>human genomics with GeneCards

by Stelzer Gil, Dalah Irina, Stein Tsippi, Satanower Yigeal, Rosen Naomi, Nativ Noam, Oz-Levi Danit, Olender Tsviya, Belinky Frida, Bahir Iris, Krug Hagit, Perco Paul, Mayer Bernd, Kolker Eugene, Safran Marilyn, Lancet Doron
Published 2011-10-01

Inter-chromosomal variation in the pattern of human population genetic structure

by Baye Tesfaye M
Published 2011-05-01

Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases

by Fasil Tekola-Ayele, Anthony Lee, Tsegaselassie Workalemahu, Katy Sánchez-Pozos
Published 2019-04-01

The impact of genome-wide association studies on biomedical research publications

by Travis J. Struck, Brian K. Mannakee, Ryan N. Gutenkunst
Published 2018-08-01

Identification of drug repurposing candidates based on a miRNA-mediated drug and pathway network for cardiac hypertrophy and acute myocardial infarction

by Jiantao Sun, Jiemei Yang, Jing Chi, Xue Ding, Nan Lv
Published 2018-12-01

Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutations

by Zhang Guojie, Pei Zhang, Ball Edward V, Mort Matthew, Kehrer-Sawatzki Hildegard, Cooper David N
Published 2011-07-01