Related references
Note: Only part of the references are listed.Critical Evaluation of Imprinted Gene Expression by RNA-Seq: A New Perspective
Brian DeVeale et al.
PLOS GENETICS (2012)
Genes that escape from X inactivation
Joel B. Berletch et al.
HUMAN GENETICS (2011)
BEDTools: a flexible suite of utilities for comparing genomic features
Aaron R. Quinlan et al.
BIOINFORMATICS (2010)
Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome
Alexandra M. Lopes et al.
BMC GENOMICS (2010)
Triple X syndrome: a review of the literature
Maarten Otter et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Global survey of escape from X inactivation by RNA-sequencing in mouse
Fan Yang et al.
GENOME RESEARCH (2010)
Strong Purifying Selection at Genes Escaping X Chromosome Inactivation
Chungoo Park et al.
MOLECULAR BIOLOGY AND EVOLUTION (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (2010)
A review of trisomy X (47, XXX)
Nicole R. Tartaglia et al.
ORPHANET JOURNAL OF RARE DISEASES (2010)
Polymorphic Cis- and Trans-Regulation of Human Gene Expression
Vivian G. Cheung et al.
PLOS BIOLOGY (2010)
TopHat: discovering splice junctions with RNA-Seq
Cole Trapnell et al.
BIOINFORMATICS (2009)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
X-LINKED INTELLECTUAL DISABILITY: UNIQUE VULNERABILITY OF THE MALE GENOME
Roger E. Stevenson et al.
DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2009)
RNA-Seq: a revolutionary tool for transcriptomics
Zhong Wang et al.
NATURE REVIEWS GENETICS (2009)
NCBI GEO: archive for high-throughput functional genomic data
Tanya Barrett et al.
NUCLEIC ACIDS RESEARCH (2009)
Characterisation of Inactivation Domains and Evolutionary Strata in Human X Chromosome through Markov Segmentation
Ashwin Kelkar et al.
PLOS ONE (2009)
The genetic landscape of intellectual disability arising from chromosome X
Jozef Gecz et al.
TRENDS IN GENETICS (2009)
Genome partitioning of genetic variation for height from 11,214 sibling pairs
Peter M. Visscher et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
A moment-based method for estimating the proportion of true null hypotheses and its application to microarray gene expression data
Yinglei Lai
BIOSTATISTICS (2007)
The human pseudoautosomal region (PAR): Origin, function and future
A. Helena Mangs et al.
CURRENT GENOMICS (2007)
The evolution of sex-biased genes and sex-biased gene expression
Hans Ellegren et al.
NATURE REVIEWS GENETICS (2007)
Dosage compensation in mammals: fine-tuning the expression of the X chromosome
Edith Heard et al.
GENES & DEVELOPMENT (2006)
Genetic linkage of human height is confirmed to 9q22 and Xq24
YZ Liu et al.
HUMAN GENETICS (2006)
A single determinant dominates the rate of yeast protein evolution
DA Drummond et al.
MOLECULAR BIOLOGY AND EVOLUTION (2006)
X-inactivation profile reveals extensive variability in X-linked gene expression in females
L Carrel et al.
NATURE (2005)
A gene atlas of the mouse and human protein-encoding transcriptomes
AI Su et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Genetic dissection of human stature in a large sample of multiplex pedigrees
YZ Liu et al.
ANNALS OF HUMAN GENETICS (2004)
Comparative sequence and X-inactivation analyses of a domain of escape in human Xpll.2 and the conserved segment in mouse
KD Tsuchiya et al.
GENOME RESEARCH (2004)
A stain upon the silence: genes escaping X inactivation
CJ Brown et al.
TRENDS IN GENETICS (2003)
A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature
HW Deng et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Escape from X inactivation
CM Disteche et al.
CYTOGENETIC AND GENOME RESEARCH (2002)