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Дата окончания | n/a |
PR | 5 |
ИКС | n/a |
Страниц в Google | 149 |
Страниц в Яндексе | 76 |
Dmoz | Нет |
Яндекс Каталог | Нет |
Alexa Traffic Rank | Нет данных |
Alexa Country | Нет данных |
История изменения показателей | Авторизация |
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NeurOmics website – NeurOmics website
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NeurOmics website
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wikipedia.org | 29 | 9 |
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nih.gov | 22 | 8 |
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ucl.ac.uk | 14 | 9 |
650 | 3869 | 187 | |
medscape.com | 11 | 7 |
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patient.co.uk | 9 | 6 |
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facebook.com | 8 | 9 |
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bmj.com | 8 | 8 |
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mda.org | 7 | 7 |
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usf.edu | 6 | 8 |
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Еще 40 сайтов после авторизации |
Данные предоставлены сервисом semrush
Счетчик | Посетители за 24 часа | Просмотры | Просмотров на посетителя |
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Google Analytics | Нет доступа | Нет доступа | n/a |
Данные linkpad ( 16 Марта 2013 ) | |
Количество ссылок на сайт | 201 |
Количество доменов, которые ссылаются на сайт | 13 |
Количество найденных анкоров | 5 |
Исходящие (внешние) ссылки домена | 94 |
Количество доменов, на которые ссылается сайт | 79 |
Количество исходящих анкоров | 82 |
Внешние ссылки главной страницы ( 11 ) | |
youtube.com/watch?v=JxXX6L-ojF8 | W atch the video of the event |
hddennomore.com/ | HDdennomore |
dx.doi.org/10.1186/s40478-016-0407-3 | - |
rd-connect.eu | <img> |
ctsr.uniklinik-freiburg.de/ | <img> |
eurenomics.eu/ | <img> |
irdirc.org | <img> |
ec.europa.eu/index_en.htm | <img> |
cobaltapps.com/downloads/dynamik-website-builder/ | Dynamik-Gen |
studiopress.com/ | Genesis Framework |
wordpress.org/ | WordPress |
Внутренние ссылки главной страницы ( 80 ) | |
rd-neuromics.eu/ | NeurOmics website |
rd-neuromics.eu/project-welcome/ | read more |
rd-neuromics.eu/about-the-project/ | About the project |
rd-neuromics.eu/coordination-office/ | Coordination |
rd-neuromics.eu/innovation-council/ | Innovation council |
rd-neuromics.eu/pac/ | Patient advisory council |
rd-neuromics.eu/project-board/ | Project board |
rd-neuromics.eu/project-ethics-council/ | Project ethics council |
rd-neuromics.eu/scientific-advisory-board/ | Scientific advisory board |
rd-neuromics.eu/news-events/news/ | Wirth Lab team identify the genetic variations in gene that are responsible for a new type of muscular atrophy |
rd-neuromics.eu/news-events/ | News & events |
rd-neuromics.eu/annual-project-reports/ | Annual project reports |
rd-neuromics.eu/news-events/newsletter/ | Newsletter |
rd-neuromics.eu/eu-data-protection-regulation/ | Draft of EU data protection regulation – Concerns raised over draft of EU data protection regulation |
rd-neuromics.eu/diseases/ | Disease overview |
rd-neuromics.eu/disease/ataxia/ | Ataxia |
rd-neuromics.eu/disease/congenital-muscular-dystrophy/ | Congenital muscular dystrophy |
rd-neuromics.eu/disease/congenital-myasthenic-syndrome/ | Congenital myasthenic syndrome |
rd-neuromics.eu/disease/fronto-temporal-lobe-dementia/ | Fronto-temporal lobe dementia |
rd-neuromics.eu/disease/hereditary-motor-neuropathies-charco... | Hereditary motor neuropathies – Charcot-Marie-Tooth disease |
rd-neuromics.eu/disease/hereditary-spastic-paraplegias/ | Hereditary spastic paraplegias |
rd-neuromics.eu/disease/huntingtons-disease/ | Huntington’s disease |
rd-neuromics.eu/disease/muscular-channelopathy/ | Muscular channelopathy |
rd-neuromics.eu/disease/muscular-dystrophy/ | Muscular dystrophy |
rd-neuromics.eu/disease/spinal-muscular-atrophy-lower-motor-... | Spinal muscular atrophy – Lower motor neuron disease |
rd-neuromics.eu/workpackages/ | Workpackages |
rd-neuromics.eu/workpackage/wp1/ | 1 – Deep phenotype analysis in pre-symptomatic and symptomatic NDD/NMD patients |
rd-neuromics.eu/workpackage/wp2/ | 2 – Identification of novel disease genes in NDD/NMD patients |
rd-neuromics.eu/workpackage/wp3/ | 3 – Identification of modifying factors in cohorts enriched by deep phenotyping |
rd-neuromics.eu/workpackage/wp4/ | 4 – Identification of hypothesis-driven biomarkers for disease progression |
rd-neuromics.eu/workpackage/wp5/ | 5 – Development and implementation of disease group overlapping NGS-based diagnostic panels |
rd-neuromics.eu/workpackage/wp6/ | 6 – Diagnostic read outs for predicting disease modification |
rd-neuromics.eu/workpackage/wp7/ | 7 – Omics-based biomarkers for progression and therapy monitoring related to disease pathways |
rd-neuromics.eu/workpackage/wp8/ | 8 – Bioinformatic tools for diagnostic prediction |
rd-neuromics.eu/workpackage/wp9/ | 9 – Omics-assisted therapy development |
rd-neuromics.eu/workpackage/wp10/ | 10 – Elucidation of pathogenesis and monitoring of treatment |
rd-neuromics.eu/workpackage/wp11/ | 11 – Modifier gene identification, prioritization and study |
rd-neuromics.eu/workpackage/wp12/ | 12 – Impact and communication |
rd-neuromics.eu/workpackage/wp13/ | 13 – Research infrastructure |
rd-neuromics.eu/workpackage/wp14/ | 14 – Project Management |
rd-neuromics.eu/project-partners/ | Project partners |
rd-neuromics.eu/organization/agilent/ | Agilent Technologies |
rd-neuromics.eu/organization/ariadne/ | Ariadne Diagnostics, LLC |
rd-neuromics.eu/organization/bio-prodict/ | Bio-Prodict |
rd-neuromics.eu/organization/cambridge-university/ | Cambridge University |
rd-neuromics.eu/organization/decode-genetics/ | deCODE genetics |
rd-neuromics.eu/organization/german-center-for-neurodegenera... | German Center for Neurodegenerative Diseases (DZNE) |
rd-neuromics.eu/organization/inserm/ | Institut National de la Santé et de la Recherche Médicale |
rd-neuromics.eu/organization/lumc/ | Leiden University Medical Center – LUMC |
rd-neuromics.eu/organization/newcastle-university/ | Newcastle University |
rd-neuromics.eu/organization/profilomic/ | Profilomic |
rd-neuromics.eu/organization/universitatsklinikum-freiburg/ | Universitätsklinikum Freiburg |
rd-neuromics.eu/organization/universite-daix-marseille/ | Universite d’Aix Marseille |
rd-neuromics.eu/organization/university-college-london-ich/ | University College London – ICH |
rd-neuromics.eu/organization/university-college-london-ion/ | University College London – IoN |
rd-neuromics.eu/organization/ucl-mrc/ | University College London – MRC |
rd-neuromics.eu/organization/university-hospital-cologne/ | University Hospital Cologne |
rd-neuromics.eu/organization/university-of-antwerp-cde/ | University of Antwerp – CDE |
rd-neuromics.eu/organization/university-of-ferrara/ | University of Ferrara |
rd-neuromics.eu/organization/university-of-milan/ | University of Milan |
rd-neuromics.eu/organization/university-tuebingen/ | University of Tübingen |
rd-neuromics.eu/organization/university-of-western-australia... | University of Western Australia |
# | - |
rd-neuromics.eu/intranet | Intranet |
rd-neuromics.eu/publication-highlights/ | Publication highlights |
rd-neuromics.eu/publication/229th-enmc-international-worksho... | 229th ENMC international workshop: Limb girdle muscular dystrophies – nomenclature and reformed classification, 17-19 March 2017... |
rd-neuromics.eu/publication/tracking-disease-progression-non... | Tracking disease progression non‐invasively in Duchenne and Becker muscular dystrophies |
rd-neuromics.eu/publication/survival-in-patients-with-spinoc... | Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study |
rd-neuromics.eu/publication/recessive-variants-of-musk-are-a... | Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness |
rd-neuromics.eu/publication/rd-connect-neuromics-and-eurenom... | RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases |
rd-neuromics.eu/publication/the-beta-adrenergic-agonist-salb... | The Beta-Adrenergic Agonist Salbutamol Modulates Neuromuscular Junction Formation in Zebrafish Models of Human Myasthenic Syndr... |
rd-neuromics.eu/publication/rare-non-synonymous-variants-in-... | Rare non-synonymous variants in SORT1 are associated with increased risk for frontotemporal dementia |
rd-neuromics.eu/publication/pfn2-and-gamt-as-common-molecula... | PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease |
rd-neuromics.eu/publication/cross-sectional-serum-metabolomi... | Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy |
rd-neuromics.eu/publication/harmonising-phenomics-informatio... | Harmonising phenomics information for a better interoperability in the rare disease field |
rd-neuromics.eu/resources/ | Resources |
rd-neuromics.eu/our-privacy-policy/ | Our privacy policy |
rd-neuromics.eu/publication/homozygous-mutations-in-vamp1-ca... | Homozygous mutations in VAMP1 cause a presynaptic congenital myasthenic syndrome |
rd-neuromics.eu/neuroSite/wp-login.php | Log in |
rd-neuromics.eu/neuroSite/cookie-policy | - Find out more - |
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