Chuong J, Ben Nun N, Suresh I, Matthews J, De T, Avecilla G
Elife. 2025; 13.
PMID: 39899365
PMC: 11790251.
DOI: 10.7554/eLife.98934.
Chuong J, Ben Nun N, Suresh I, Matthews J, De T, Avecilla G
bioRxiv. 2024; .
PMID: 39464144
PMC: 11507740.
DOI: 10.1101/2024.05.03.589936.
Yoshioka Y, Taniguchi J, Homma H, Tamura T, Fujita K, Inotsume M
Commun Med (Lond). 2023; 3(1):170.
PMID: 38017287
PMC: 10684506.
DOI: 10.1038/s43856-023-00400-y.
Mohiuddin M, Kooy R, Pearson C
Front Genet. 2022; 13:983668.
PMID: 36226191
PMC: 9550265.
DOI: 10.3389/fgene.2022.983668.
Reilly M, Rossor A
J Neurol Neurosurg Psychiatry. 2020; 91(11):1132-1136.
PMID: 32769113
PMC: 7415072.
DOI: 10.1136/jnnp-2020-323016.
2018 Victor A. McKusick Leadership Award: Molecular Mechanisms for Genomic and Chromosomal Rearrangements.
Lupski J
Am J Hum Genet. 2019; 104(3):391-406.
PMID: 30849326
PMC: 6407437.
DOI: 10.1016/j.ajhg.2018.12.018.
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency.
Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery A
J Clin Invest. 2018; 129(2):583-597.
PMID: 30422821
PMC: 6355244.
DOI: 10.1172/JCI124011.
exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E.
Wang D, Wu X, Bai Y, Zaidman C, Grider T, Kamholz J
Ann Clin Transl Neurol. 2017; 4(4):236-245.
PMID: 28382305
PMC: 5376752.
DOI: 10.1002/acn3.395.
Major influence of repetitive elements on disease-associated copy number variants (CNVs).
Cardoso A, Oliveira M, Amorim A, Azevedo L
Hum Genomics. 2016; 10(1):30.
PMID: 27663310
PMC: 5035501.
DOI: 10.1186/s40246-016-0088-9.
Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.
Yuan B, Neira J, Gu S, Harel T, Liu P, Briceno I
Hum Genet. 2016; 135(10):1161-74.
PMID: 27386852
PMC: 5021589.
DOI: 10.1007/s00439-016-1703-5.
Nonrecurrent 17p11.2p12 Rearrangement Events that Result in Two Concomitant Genomic Disorders: The PMP22-RAI1 Contiguous Gene Duplication Syndrome.
Yuan B, Harel T, Gu S, Liu P, Burglen L, Chantot-Bastaraud S
Am J Hum Genet. 2015; 97(5):691-707.
PMID: 26544804
PMC: 4667131.
DOI: 10.1016/j.ajhg.2015.10.003.
Structural variation mutagenesis of the human genome: Impact on disease and evolution.
Lupski J
Environ Mol Mutagen. 2015; 56(5):419-36.
PMID: 25892534
PMC: 4609214.
DOI: 10.1002/em.21943.
Mechanism, prevalence, and more severe neuropathy phenotype of the Charcot-Marie-Tooth type 1A triplication.
Liu P, Gelowani V, Zhang F, Drory V, Ben-Shachar S, Roney E
Am J Hum Genet. 2014; 94(3):462-9.
PMID: 24530202
PMC: 3951935.
DOI: 10.1016/j.ajhg.2014.01.017.
Functional characterization of the human mariner transposon Hsmar2.
Gil E, Bosch A, Lampe D, Lizcano J, Perales J, Danos O
PLoS One. 2013; 8(9):e73227.
PMID: 24039890
PMC: 3770610.
DOI: 10.1371/journal.pone.0073227.
The PMP22 gene and its related diseases.
Li J, Parker B, Martyn C, Natarajan C, Guo J
Mol Neurobiol. 2012; 47(2):673-98.
PMID: 23224996
PMC: 3594637.
DOI: 10.1007/s12035-012-8370-x.
Multiple cellular mechanisms prevent chromosomal rearrangements involving repetitive DNA.
George C, Alani E
Crit Rev Biochem Mol Biol. 2012; 47(3):297-313.
PMID: 22494239
PMC: 3337352.
DOI: 10.3109/10409238.2012.675644.
Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.
Itsara A, Vissers L, Steinberg K, Meyer K, Zody M, Koolen D
Am J Hum Genet. 2012; 90(4):599-613.
PMID: 22482802
PMC: 3322237.
DOI: 10.1016/j.ajhg.2012.02.013.
Mechanisms for recurrent and complex human genomic rearrangements.
Liu P, Carvalho C, Hastings P, Lupski J
Curr Opin Genet Dev. 2012; 22(3):211-20.
PMID: 22440479
PMC: 3378805.
DOI: 10.1016/j.gde.2012.02.012.
Genomic medicine and neurological disease.
Boone P, Wiszniewski W, Lupski J
Hum Genet. 2011; 130(1):103-21.
PMID: 21594611
PMC: 3133694.
DOI: 10.1007/s00439-011-1001-1.
Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene.
Clarke N, Maugenre S, Vandebrouck A, Urtizberea J, Willer T, Peat R
Eur J Hum Genet. 2011; 19(4):452-7.
PMID: 21248746
PMC: 3060325.
DOI: 10.1038/ejhg.2010.212.