Inventaire - your friends and communities are your best library

Extreme enrichment of VNTR-associated polymorphicity in human subtelomeres: genes with most VNTRs are predominantly expressed in the brain

author

Wim Meert

Jonas Korlach

Marcel J T Reinders

Henne Holstege

published in: Translational Psychiatry

date of publication: 2020-11-02

Cites articles 81

Date

Title

Authors

2020-02-03

SciPy 1.0: fundamental algorithms for scientific computing in Python

Ralf Gommers, Matt Haberland, Tyler Reddy, Stéfan J. van der Walt, K. Jarrod Millman, Andrew Nelson, Denis Laxalde, Antônio H Ribeiro, Paul van Mulbregt, Travis E. Oliphant, Matthew Brett, Eric Wieser, Anne M. Archibald, David Cournapeau, Pearu Peterson, Evgeni Burovski, Pauli Virtanen, Warren Weckesser, Josef Perktold
2019-04-16

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Ashley D Sanders, Xuefang Zhao, David Porubsky, Tobias Rausch, Eugene J Gardner, Li Guo, Robert E Handsaker, Susan Fairley, Aaron M Wenger, Danny Antaki, Peter A Audano, Xintong Chen, Chen-Shan Chin, Zechen Chong, Deanna M. Church, Laura Clarke, David U Gorkin, Victor Guryev, Haynes Heaton, Jonas Korlach, Joyce Lee, Sascha Meiers, Katherine M Munson, Fábio C P Navarro, Yunjiang Qiu, Ernesto Lowy, Sergei Yakneen, Bing Ren, Paul Flicek, Ken Chen, Pui-Yan Kwok, Jonathan Sebat, Xinghua Shi, Tobias Marschall, Jan Korbel, Evan E. Eichler, Steven A McCarroll, Mark Bender Gerstein, Gabor T Marth, Adrian M Stütz, Fereydoun Hormozdiari, Mark J P Chaisson
2019-01-17

Characterizing the Major Structural Variant Alleles of the Human Genome

Arvis Sulovari, Melanie Sorensen, Sean D. McGrath, Wesley C Warren, Evan E. Eichler
2019-01-01

The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019

Annalisa Buniello, Laura W Harris, James D Hayhurst, Aoife C McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis, Daniel Suveges, Stephen Trevanion, Paul Flicek, Tony Burdett, Fiona Cunningham, Helen Parkinson, Lucia A Hindorff, Patricia L Whetzel, Maria Cerezo, M Ridwan Amode, Harpreet S Riat, Peggy Hall, Heather A Junkins
2019-03-01

Genetic influences on susceptibility to rheumatoid arthritis in African-Americans

Leah C. Kottyan, Carl D. Langefeld
2018-08-09

Characterization of a Human-Specific Tandem Repeat Associated with Bipolar Disorder and Schizophrenia
2018-02-05

Tandem repeats mediating genetic plasticity in health and disease.

Anthony J Hannan
2018-01-01

Repeat expansion diseases.
2018-09-26

Centenarian controls increase variant effect sizes by an average twofold in an extreme case-extreme control analysis of Alzheimer's disease.

Sven J van der Lee, Najada Stringa, Philip Scheltens, Wiesje van der Flier, Henne Holstege, Hanne Meijers-Heijboer, Iris E Jansen, Marc Hulsman, Marcel J T Reinders, Natasja M van Schoor
2018-01-11

R-loops: targets for nuclease cleavage and repeat instability

Catherine H Freudenreich
2018-11-21

Somatic APP gene recombination in Alzheimer's disease and normal neurons

William J Romanow
2018-02-01

Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair.

Carla Gallo, Fuduan Peng, Susan Walsh, Cornelia M. van Duijn, Maria Cátira Bortolini, Wojciech Branicki, Tim Spector
2018-12-11

Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study

Catherine John, María Soler Artigas, Richard Packer, John W. Holloway, Ratko Djukanovic, John D Blakey, Martin D Tobin, Chris Brightling, Louise Wain, Ian Sayers, David C. Nickle
2017-04-10

Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly

Sean D. McGrath, Kerstin Howe, Terence D. Murphy, Kim D. Pruitt, William Chow, Tim Hubbard, Glen Threadgold, James Torrance, Laura Clarke, Sergey Koren, Heng Li, Adam Phillippy, Paul Flicek, Deanna M. Church, Evan E. Eichler, Richard M. Durbin, Chen-Shan Chin, Milinn Kremitzki, Tina A Graves-Lindsay, Paul Peluso, Francoise Thibaud-Nissen
2017-10-30

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.

Hansjörg Baurecht, Kimberley Burrows, Lars G Fritsche, David L. Duffy, Stephan Weidinger, David A Hinds, Franz Rüschendorf, Edward Mountjoy, Jonas B Nielsen, Jie Zheng, Robert Karlsson, Yi Lu, Rick Jansen, Jonathan Beesley, Jenny van Dongen, Kristian Hveem, Arnulf Langhammer, Patrik K E Magnusson, Dorret Boomsma, Konstantin Strauch, Jouke-Jan Hottenga, Lavinia Paternoster, Ronald B. Melles, Andre Franke, 23andMe Research Team, So-Young Lee
2016-06-06

Unstable repeat expansion in major psychiatric disorders: two decades on, is dynamic DNA back on the menu?
2016-11-28

Discovery and genotyping of structural variation from long-read haploid genome sequence data

Katherine M Munson, John Huddleston, Zev N Kronenberg, Evan E. Eichler, Mark J P Chaisson
2016-10-17

Phased diploid genome assembly with single-molecule real-time sequencing

Chen-Shan Chin, Fritz Sedlazeck, Christopher Dunn, Grant Cramer, Joseph R. Ecker, Dario Cantu
2016-08-03

Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder

Deborah Dewey, Stephen W. Scherer, A. Micheil Innes, Jillian S Parboosingh, François P. Bernier
2016-09-12

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Jennifer A Smith, Albert V. Smith, Han Chen, Panos Deloukas, Cornelia M. van Duijn, Heribert Schunkert, André Uitterlinden, Eric Boerwinkle, Mathias Gorski, Christopher Newton-Cheh, Omri Gottesman, Charles Kooperberg, Stefan Weiss, Claude Bouchard, Jessica D. Faul, I-Te Lee, Alanna Morrison, Marcus Dörr, Najaf Amin, Oscar H Franco, Ramachandran S. Vasan, Uwe Völker, Jerome I Rotter, Man Li, Tamara B. Harris, Nilesh Samani, Ruth J. Loos, Erwin Böttinger, Vilmundur Gudnason, Sekar Kathiresan, Christian Fuchsberger, Lenore J Launer, Yongmei Liu, Bruce M. Psaty, Myriam Fornage, Sharon L R Kardia, Joshua C Bis, Ingrid B Borecki, Paul Ridker, Adolfo Correa, Nora Franceschini, Daniel I Chasman, Digna R. Velez Edwards, Todd L. Edwards, Kent D Taylor, Krystal S. Tsosie, Jennifer A. Brody, Yii-Der Ida Chen, Johanna Jakobsdottir, Wayne Huey-Herng Sheu, George J Papanicolaou, Alexander P Reiner, Kenneth M Rice, Lisa W. Martin, Paul L Auer, Jeanette M Stafford, Nathan O Stitziel, Leslie J Raffel, Christopher J O'Donnell, Elias L Salfati, Stephan B Felix, David R Weir, Georg B Ehret, Xiuqing Guo, Santhi K Ganesh, Audrey Chu, Cristian Pattaro, Aravinda Chakravarti
2015-11

Genetic variation and the de novo assembly of human genomes

Evan E. Eichler, Mark J P Chaisson
2015-07-22

A recurrent copy number variation of the NEB triplicate region: only revealed by the targeted nemaline myopathy CGH array

Ari Löytynoja, Vilma-Lotta Lehtokari, Katarina Pelin
2015-04-01

Gene length matters in neurons

Mark J. Zylka
2015-06-29

Assembly and diploid architecture of an individual human genome via single-molecule technologies

Tobias Rausch, Scott C Blanchard, Chen-Shan Chin, Jan Korbel, Oscar Franzén, Robert Sebra, Gintaras Deikus, Christopher E. Mason, Eric E Schadt
2014-05

Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis

Hanne Meijers-Heijboer, Daoud Sie, Martijn Brugman, Bauke Ylstra
2014-01-08

Role of the DLGAP2 gene encoding the SAP90/PSD-95-associated protein 2 in schizophrenia

Min-Chih Cheng, Chia-Hsiang Chen
2014-12-11

An evolutionary arms race between KRAB zinc-finger genes ZNF91/93 and SVA/L1 retrotransposons

David Haussler, Adam D Ewing, Benedict Paten, Maximilian Haeussler
2013-03-19

The VNTR in complex disorders: the forgotten polymorphisms? A functional way forward?
2013-07-06

A common 56-kilobase deletion in a primate-specific segmental duplication creates a novel butyrophilin-like protein

Xavier Estivill i Pallejà, Raquel Rabionet
2013-08-28

Topoisomerases facilitate transcription of long genes linked to autism

Angela Mabb, Hsien-Sung Huang, Brandon L. Pearson, Ian King, Mark J. Zylka, Terry Magnuson, Joshua Starmer
2011-05

A framework for variation discovery and genotyping using next-generation DNA sequencing data

Mark Joseph Daly, David Altshuler, Stacey Gabriel, Manuel Antonio Rivas
2011-03-15

Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites

Jean-Charles Lambert, Nathalie Brouwers, Rik Vandenberghe, Philippe Amouyel, Florence Pasquier, Christine Van Broeckhoven

Article - wd:Q101165845

Welcome to Inventaire

the library of your friends and communities

learn more