Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Audrey V. Grant"'
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 5 (2023)
Externí odkaz:
https://doaj.org/article/fea0c270a4484fbf902c26c68f1e6905
Publikováno v:
STAR Protocols, Vol 4, Iss 1, Pp 101966- (2023)
Summary: To address the need for systematic investigation of the phenome enabled by ever-growing genotype and phenotype data, we describe our step-by-step software implementation of a graph-embedded topic model, including data preprocessing, graph le
Externí odkaz:
https://doaj.org/article/72fbed7ceb0e46ff95db89ac4042f8db
Publikováno v:
iScience, Vol 25, Iss 6, Pp 104390- (2022)
Summary: Large biobank repositories of clinical conditions and medications data open opportunities to investigate the phenotypic disease network. We present a graph embedded topic model (GETM). We integrate existing biomedical knowledge graph informa
Externí odkaz:
https://doaj.org/article/2bf455a4a1e44d259534d7701752f02f
Autor:
Xiang Ao, Marc Parisien, Maha Zidan, Audrey V. Grant, Amy E. Martinsen, Bendik S. Winsvold, Luda Diatchenko
Publikováno v:
Pain.
Autor:
Marc Parisien, Lucas V. Lima, Concetta Dagostino, Nehme El-Hachem, Gillian L. Drury, Audrey V. Grant, Jonathan Huising, Vivek Verma, Carolina B. Meloto, Jaqueline R. Silva, Gabrielle G. S. Dutra, Teodora Markova, Hong Dang, Philippe A. Tessier, Gary D. Slade, Andrea G. Nackley, Nader Ghasemlou, Jeffrey S. Mogil, Massimo Allegri, Luda Diatchenko
Publikováno v:
Science Translational Medicine. 14
The transition from acute to chronic pain is critically important but not well understood. Here, we investigated the pathophysiological mechanisms underlying the transition from acute to chronic low back pain (LBP) and performed transcriptome-wide an
Autor:
Hans Markus Munter, Simon Gravel, Chief Ben-Eghan, Rosie Sun, Jose Sergio Hleap, Charles Dupras, Alex Diaz-Papkovich, Audrey V Grant
Publikováno v:
Nature. 585:184-186
Efforts to build representative studies are defeated when scientists discard data from certain groups. Instead, researchers should work to balance statistical needs with fairness. Efforts to build representative studies are defeated when scientists d
Autor:
Chief, Ben-Eghan, Rosie, Sun, Jose Sergio, Hleap, Alex, Diaz-Papkovich, Hans Markus, Munter, Audrey V, Grant, Charles, Dupras, Simon, Gravel
Publikováno v:
Nature. 585(7824)
Autor:
Alexandre Bolze, Avinash Abhyankar, Audrey V Grant, Bhavi Patel, Ruchi Yadav, Minji Byun, Daniel Caillez, Jean-Francois Emile, Marçal Pastor-Anglada, Laurent Abel, Anne Puel, Rajgopal Govindarajan, Loic de Pontual, Jean-Laurent Casanova
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e29708 (2012)
We investigated two siblings with granulomatous histiocytosis prominent in the nasal area, mimicking rhinoscleroma and Rosai-Dorfman syndrome. Genome-wide linkage analysis and whole-exome sequencing identified a homozygous frameshift deletion in SLC2
Externí odkaz:
https://doaj.org/article/7b764a6538f44a09bd68aa0cb8662ff9
Autor:
Stéphanie Boisson-Dupuis, Jamila El Baghdadi, Nima Parvaneh, Aziz Bousfiha, Jacinta Bustamante, Jacqueline Feinberg, Arina Samarina, Audrey V Grant, Lucile Janniere, Naima El Hafidi, Amal Hassani, Daniel Nolan, Jilali Najib, Yildiz Camcioglu, Nevin Hatipoglu, Cigdem Aydogmus, Gonul Tanir, Caner Aytekin, Melike Keser, Ayper Somer, Guside Aksu, Necil Kutukculer, Davood Mansouri, Alireza Mahdaviani, Setareh Mamishi, Alexandre Alcais, Laurent Abel, Jean-Laurent Casanova
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e18524 (2011)
In the last decade, autosomal recessive IL-12Rβ1 deficiency has been diagnosed in four children with severe tuberculosis from three unrelated families from Morocco, Spain, and Turkey, providing proof-of-principle that tuberculosis in otherwise healt
Externí odkaz:
https://doaj.org/article/371611f76da547a09747d5270c01ce63
Autor:
Avner Bar-Hen, Cheikh Loucoubar, Isabelle Casademont, Joseph Faye, Audrey V. Grant, Jean-François Bureau, Mamadou Diop, Jean-François Trape, Adama Tall, Anavaj Sakuntabhai, Abdoulaye Badiane, Ndjido Ardo Bar, Freddy Cliquet, Fatoumata Diene Sarr, Mark Lathrop, Richard Paul, Benno Schwikowski
Publikováno v:
Briefings in Bioinformatics
Briefings in Bioinformatics, Oxford University Press (OUP), 2017, 18 (3), pp.394-402. ⟨10.1093/bib/bbw039⟩
Briefings in Bioinformatics, 2017, 18 (3), pp.394-402. ⟨10.1093/bib/bbw039⟩
Briefings in Bioinformatics, Oxford University Press (OUP), 2017, 18 (3), pp.394-402. ⟨10.1093/bib/bbw039⟩
Briefings in Bioinformatics, 2017, 18 (3), pp.394-402. ⟨10.1093/bib/bbw039⟩
International audience; The era of genome-wide association studies (GWAS) has led to the discovery of numerous genetic variants associated with disease. Better understanding of whether these or other variants interact leading to differential risk com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9169cf639d77a808cf24e11031eb6a43
https://hal-pasteur.archives-ouvertes.fr/pasteur-02068171/file/bbw039.pdf
https://hal-pasteur.archives-ouvertes.fr/pasteur-02068171/file/bbw039.pdf