A. Lemainque

发表

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34

M. Lathrop, C. Petit, M. Mustapha, 2002, European Journal of Human Genetics.

De novo assembly and annotation of three Leptosphaeria genomes using Oxford Nanopore MinION sequencing

P. Wincker, A. Couloux, A. Lemainque, 2018, Scientific Data.

FORK-seq: replication landscape of the Saccharomyces cerevisiae genome by nanopore sequencing

B. Audit, A. Lemainque, C. Cruaud, 2020, Genome Biology.

FORK-seq: replication landscape of the Saccharomyces cerevisiae genome by nanopore sequencing

B. Audit, A. Lemainque, C. Cruaud, 2020, Genome Biology.

Invasions Toolkit: Current Methods for Tracking the Spread and Impact of Invasive Species

David A. Bohan, A. Lemainque, D. Bohan, 2017 .

The Rosa genome provides new insights into the domestication of modern roses

P. Wincker, J. Gouzy, Chang Liu, 2018, Nature Genetics.

Chromosome reciprocal translocations have accompanied subspecies evolution in bananas

A. Lemainque, K. Labadie, N. Yahiaoui, 2020, The Plant journal : for cell and molecular biology.

Two large reciprocal translocations characterized in the disease resistance-rich burmannica genetic group of Musa acuminata

A. Lemainque, C. Cruaud, K. Labadie, 2019, Annals of botany.

Chromosome-scale assemblies of plant genomes using nanopore long reads and optical maps

F. Denoeud, P. Wincker, V. Barbe, 2018, Nature Plants.

Genome evolution across 1,011 Saccharomyces cerevisiae isolates

Stefan Engelen, Karine Labadie, Patrick Wincker, 2018, Nature.

High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Using Nanopore MinION Sequencing

Patrick Wincker, Jean-Marc Aury, Anne Friedrich, 2017, G3: Genes, Genomes, Genetics.

High-quality de novo genome assembly of the Dekkera bruxellensis UMY321 yeast isolate using Nanopore MinION sequencing

P. Wincker, A. Lemainque, J. Aury, 2017, bioRxiv.

Oak genome reveals facets of long lifespan

Olivier Panaud, Hadi Quesneville, Franck Salin, 2018, Nature Plants.

Evidence for linkage of a new region (11p14) to eczema and allergic diseases

J. Bousquet, I. Annesi-Maesano, M. Lathrop, 2007, Human Genetics.

Viral to metazoan marine plankton nucleotide sequences from the Tara Oceans expedition

Francisco M. Cornejo-Castillo, G. Cochrane, P. Bork, 2017, Scientific Data.

Genome assembly using Nanopore-guided long and error-free DNA reads

Stefan Engelen, Mohammed-Amin Madoui, Adriana Alberti, 2015, BMC Genomics.

Estimation of the inbreeding coefficient through use of genomic data.

Bernard Prum, Arnaud Lemainque, Elizabeth A Thompson, 2003, American journal of human genetics.

A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene

A. Lemainque, C. Bönnemann, N. Romero, 2002, Annals of neurology.

Long-read assembly of the Brassica napus reference genome Darmor-bzh

Corinne Da Silva, F. Denoeud, P. Wincker, 2020, GigaScience.

SQK-MAP006 protocol for library preparation for Nanopore sequencing v1 (protocols.io.gvvbw66)

Stefan Engelen, Patrick Wincker, Anne Friedrich, 2016 .

Amish brittle hair syndrome gene maps to 7p14.1

Arnaud Lemainque, Charles E Jackson, A. Lemainque, 2005, American journal of medical genetics. Part A.

SRPX2 mutations in disorders of language cortex and cognition.

Marie-Noëlle Metz-Lutz, Edouard Hirsch, Sandrine Pereira, 2006, Human molecular genetics.

Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes.

A. Lemainque, C. Julier, S. Duchatelet, 2005, Human molecular genetics.

Colonization kinetics and implantation follow-up of the sewage microbiome in an urban wastewater treatment plant

A. Lemainque, K. Labadie, C. Madigou, 2020, Scientific Reports.

Lifespan prolonging mechanisms and insulin upregulation without fat accumulation in long-lived reproductives of a higher termite

E. Bornberg-Bauer, T. V. Van Dooren, Laure‐Anne Poissonnier, 2021, Communications Biology.

Extreme longevity of highly fecund termite queens achieved by mitochondrial and insulin upregulation without harmful lipid signatures or accumulation

E. Bornberg-Bauer, T. V. Van Dooren, Laure‐Anne Poissonnier, 2021 .

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection.

A. Fischer, J. Casanova, A. Lemainque, 2005, The Journal of clinical investigation.

A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease

J. Casanova, C. Picard, A. Lemainque, 2006, Journal of Medical Genetics.

Structural characterization and mapping of functional EST-SSR markers in Theobroma cacao

A. Lemainque, A. Risterucci, B. Courtois, 2011, Tree Genetics & Genomes.

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

C Henry, S Cichon, B Etain, 2006, Molecular Psychiatry.

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.

A. Lemainque, C. Julier, S. Azar, 2008, Human molecular genetics.

Molecular linkage maps: strategies, resources and achievements.

A. Lemainque, R. Testolin, G. Cipriani, 2011 .

A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3‐p15.1

Christian Dina, Arnaud Lemainque, Francis Vasseur, 2002, Annals of neurology.

Complete Genome Sequence of Bacillus methylotrophicus Strain B25, a Potential Plant Growth-Promoting Rhizobacterium

C. Médigue, A. Lemainque, D. Vallenet, 2016, Genome Announcements.

Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.

A. Monaco, M. Lathrop, A. Lemainque, 2001, American journal of human genetics.

Chromosome-scale assemblies of plant genomes using nanopore long reads and optical maps

F. Denoeud, P. Wincker, V. Barbe, 2018, Nature Plants.

Recombination and Large Structural Variations Shape Interspecific Edible Bananas Genomes

A. Lemainque, N. Yahiaoui, M. Rouard, 2018, Molecular biology and evolution.

The Rosa genome provides new insights into the domestication of modern roses

P. Wincker, J. Gouzy, Chang Liu, 2018, Nature Genetics.

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.

T. Wienker, A. Lemainque, F. Hildebrandt, 2003, Journal of the American Society of Nephrology : JASN.

Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.

J. Morissette, N. Laurin, A. Lemainque, 2001, American journal of human genetics.

Evidence for gene × smoking exposure interactions in a genome-wide linkage screen of asthma and bronchial hyper-responsiveness in EGEA families

M. Lathrop, A. Lemainque, V. Siroux, 2007, European Journal of Human Genetics.

Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families.

J. Bousquet, I. Annesi-Maesano, M. Lathrop, 2004, Human molecular genetics.

Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma

J. Bousquet, I. Annesi-Maesano, M. Lathrop, 2005, Genes and Immunity.

Telomere-to-telomere gapless chromosomes of banana using nanopore sequencing

P. Wincker, A. Lemainque, J. Aury, 2021, Communications Biology.

de novo assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer

Stefan Engelen, Patrick Wincker, Jean-Marc Aury, 2016, bioRxiv.

Long-read assembly of the Brassica napus reference genome Darmor-bzh

Corinne Da Silva, F. Denoeud, P. Wincker, 2020, bioRxiv.

Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19q.

K. Clément, C. Dina, D. Meyre, 2004, Diabetes.

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

S. Virgiliis, A. Lemainque, M. Babron, 2001, Annals of human genetics.

The canosinase gene (CNDP1) is not a protection factor of diabetic nephropathy in type 1 diabetics

M. Farrall, H. Parving, D. Trégouët, 2006 .

Genome-wide mapping of individual replication fork velocities using nanopore sequencing

B. Audit, A. Lemainque, C. Cruaud, 2022, Nature Communications.

Mapping DNA replication with nanopore sequencing

B. Audit, A. Lemainque, C. Cruaud, 2018 .

Correction: Insight into the Wild Origin, Migration and Domestication History of the Fine Flavour Nacional Theobroma cacao L. Variety from Ecuador

A. Lemainque, A. Risterucci, B. Courtois, 2013, PLoS ONE.

Insight into the Wild Origin, Migration and Domestication History of the Fine Flavour Nacional Theobroma cacao L. Variety from Ecuador

A. Lemainque, A. Risterucci, B. Courtois, 2012, PloS one.

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.

M. Ruberg, M. Welter, A. Durr, 2004, Archives of neurology.

High-Quality de Novo Genome Assembly of the Dekkera bruxellensis Yeast Isolate Using Nanopore MinION Sequencing.

P. Wincker, A. Lemainque, J. Aury, 2017, G3.

A major susceptibility locus on chromosome 22q12 plays a critical role in the control of kala-azar.

A. Lemainque, L. Abel, B. Bucheton, 2003, American journal of human genetics.

Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families

M. Lathrop, A. Lemainque, V. Siroux, 2007, European Respiratory Journal.

ARCHIVES OF NEUROLOGY

K. Tyler, M. Ruberg, M. Welter, 2015 .

Association Mapping for Phytophthora Pod Rot Resistance in a Cacao ( Theobroma cacao L . ) Population Grown in Efombagn MIB

A. Lemainque, B. Courtois, O. Fouet, 2016 .

Meiotic Behaviors of Allotetraploid Citrus Drive the Interspecific Recombination Landscape, the Genetic Structures, and Traits Inheritance in Tetrazyg Progenies Aiming to Select New Rootstocks

A. Lemainque, P. Ollitrault, R. Morillon, 2023, Plants.

Genome assembly using Nanopore-guided long and error-free DNA reads

P. Wincker, A. Lemainque, J. Aury, 2015, BMC Genomics.

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21–12.1

M. Lathrop, C. Petit, D. Weil, 2003, European Journal of Human Genetics.

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1

M. Lathrop, C. Petit, D. Weil, 2003, European Journal of Human Genetics.