Որոնման արդյունքները - Inger‐Lise Mero
- Ցուցադրվում են 1 - 6 արդյունքները 6
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1
Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis Hanne F. Harbo, Noriko Isobe, Pål Berg‐Hansen, Steffan D. Bos, Stacy J. Caillier, Marte W. Gustavsen, Inger-Lise Mero, Elisabeth Gulowsen Celius, Stephen L. Hauser, Jorge R. Oksenberg, Pierre‐Antoine Gourraud
Հրապարակվել է 2013Artigo -
2
Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies Nathan L. Absalom, Vivian W. Y. Liao, Katrine M. Johannesen, Elena Gardella, Julia Jacobs, Gaëtan Lesca, Zeynep Gokce‐Samar, Alexis Arzimanoglou, Shimriet Zeidler, Pasquale Striano, Pierre Meyer, Ira Benkel-Herrenbrueck, Inger‐Lise Mero, Jutta Rummel, Mary Chebib, Rikke S. Møller, Philip K. Ahring
Հրապարակվել է 2022Artigo -
3
Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA Nicole Revençu, Astrid Eijkelenboom, Claire Bracquemart, Pia Alhopuro, Judith Armstrong, Eulàlia Baselga, Claudia Cesario, Maria Lisa Dentici, Mélanie Eyries, Sofia Frisk, Helena Gásdal Karstensen, Nagore Gene‐Olaciregui, Sirpa Kivirikko, Cinzia Lavarino, Inger‐Lise Mero, Rodolphe Michiels, Elisa Pisaneschi, Bitten Schönewolf‐Greulich, Ilse Wieland, Martin Zenker, Miikka Vikkula
Հրապարակվել է 2024Artigo -
4
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis Inger‐Lise Mero, Åslaug Rudjord Lorentzen, Maria Ban, C. Smestad, Elisabeth Gulowsen Celius, Jan Aarseth, Kjell‐Morten Myhr, Jenny Link, Jan Hillert, Tomas Olsson, Ingrid Kockum, Thomas Masterman, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Anu Kemppinen, Irina Elovaara, Anne Spurkland, Frank Dudbridge, Benedicte A. Lie, Hanne F. Harbo
Հրապարակվել է 2009Artigo -
5
Oligoclonal Band Status in Scandinavian Multiple Sclerosis Patients Is Associated with Specific Genetic Risk Alleles Inger‐Lise Mero, Marte W. Gustavsen, Hanne Skarpodde Sæther, Siri T. Flåm, Pål Berg‐Hansen, Helle Bach Søndergaard, Poul Erik Jensen, Tone Berge, Anja Bjølgerud, Aslaug Muggerud, Jan Aarseth, Kjell‐Morten Myhr, Elisabeth Gulowsen Celius, Finn Sellebjerg, Jan Hillert, Lars Alfredsson, Tomas Olsson, Annette Oturai, Ingrid Kockum, Benedicte A. Lie, Bettina Kulle Andreassen, Hanne F. Harbo
Հրապարակվել է 2013Artigo -
6
Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, Teppo Varilo, S. Kallio, Anu Kemppinen, Shaun Purcell, Keijo Koivisto, Pentti J. Tienari, Marja‐Liisa Sumelahti, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Arpo Aromaa, Annette Oturai, Helle Bach Søndergaard, Hanne F. Harbo, Inger‐Lise Mero, Stacey B. Gabriel, Daniel B. Mirel, Stephen L. Hauser, Ludwig Kappos, Chris H. Polman, Philip L. De Jager, David A. Hafler, Mark J. Daly, Aarno Palotie, Janna Saarela, Leena Peltonen
Հրապարակվել է 2010Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Medicine
Internal medicine
Genotype
Immunology
Multiple sclerosis
Single-nucleotide polymorphism
Allele
Antigen
Genetic association
Genome-wide association study
Human leukocyte antigen
SNP
Cohort
Odds ratio
Phenotype
Allele frequency
Bioinformatics
Case-control study
Disease
Epilepsy
GABAA receptor
GABAergic
Genetic testing
Haplotype
Human genetics
Hypotonia
Locus (genetics)