Titre : Variation génétique

Variation génétique : Questions médicales fréquentes

Questions fréquentes et termes MeSH associés

Diagnostic 5

#1

Comment détecte-t-on une variation génétique ?

On utilise des tests génétiques comme le séquençage de l'ADN pour identifier les variations.
Tests génétiques Séquençage de l'ADN
#2

Quels signes indiquent une variation génétique ?

Des anomalies dans les résultats de tests génétiques peuvent signaler une variation.
Anomalies génétiques Tests de dépistage
#3

Les variations génétiques sont-elles héréditaires ?

Oui, certaines variations peuvent être transmises de génération en génération.
Hérédité Transmission génétique
#4

Quel rôle joue le génome dans le diagnostic ?

Le génome fournit des informations sur les variations pouvant causer des maladies.
Génome Maladies génétiques
#5

Peut-on identifier des variations par imagerie médicale ?

Non, l'imagerie ne détecte pas les variations génétiques, mais les effets des maladies.
Imagerie médicale Maladies héréditaires

Symptômes 5

#1

Quels symptômes sont liés aux variations génétiques ?

Les symptômes varient selon la maladie, incluant des troubles métaboliques ou neurologiques.
Symptômes Troubles génétiques
#2

Les variations génétiques causent-elles des maladies ?

Oui, certaines variations peuvent être responsables de maladies héréditaires.
Maladies héréditaires Variations génétiques
#3

Comment les variations affectent-elles le développement ?

Elles peuvent influencer le développement physique et cognitif, entraînant des retards.
Développement Retards de développement
#4

Les symptômes apparaissent-ils à tout âge ?

Pas toujours, certains symptômes peuvent se manifester à l'enfance ou à l'âge adulte.
Âge d'apparition Maladies génétiques
#5

Les variations génétiques sont-elles asymptomatiques ?

Oui, certaines variations peuvent ne pas provoquer de symptômes visibles.
Asymptomatique Variations génétiques

Prévention 5

#1

Peut-on prévenir les variations génétiques ?

Les variations génétiques sont naturelles, mais certaines maladies peuvent être évitées par des tests.
Prévention Tests génétiques
#2

Quel rôle joue le dépistage dans la prévention ?

Le dépistage permet d'identifier les risques et de prendre des mesures préventives.
Dépistage Prévention des maladies
#3

Les conseils génétiques aident-ils à prévenir ?

Oui, ils informent sur les risques et les options pour les familles à risque.
Conseils génétiques Risques héréditaires
#4

L'alimentation influence-t-elle les variations ?

Une alimentation saine peut réduire le risque de maladies liées à certaines variations.
Alimentation Facteurs de risque
#5

Les vaccinations préviennent-elles des maladies génétiques ?

Non, les vaccinations ne préviennent pas les variations génétiques, mais les maladies infectieuses.
Vaccinations Prévention des maladies infectieuses

Traitements 5

#1

Quels traitements existent pour les maladies génétiques ?

Les traitements incluent la thérapie génique, les médicaments et la gestion des symptômes.
Thérapie génique Traitements médicaux
#2

La thérapie génique est-elle efficace ?

Elle peut être efficace pour certaines maladies, mais les résultats varient selon les cas.
Thérapie génique Efficacité des traitements
#3

Peut-on prévenir les maladies par des traitements ?

Certains traitements peuvent réduire le risque de développer des maladies génétiques.
Prévention Traitements préventifs
#4

Les traitements sont-ils personnalisés ?

Oui, les traitements peuvent être adaptés en fonction des variations génétiques spécifiques.
Médecine personnalisée Traitements ciblés
#5

Quels médicaments sont utilisés pour les variations génétiques ?

Des médicaments spécifiques peuvent traiter les symptômes ou les causes des maladies génétiques.
Médicaments Traitements symptomatiques

Complications 5

#1

Quelles complications peuvent survenir ?

Les complications varient selon la maladie, incluant des troubles organiques ou fonctionnels.
Complications Troubles organiques
#2

Les variations génétiques augmentent-elles le risque de cancer ?

Oui, certaines variations génétiques sont associées à un risque accru de cancer.
Cancer Variations génétiques
#3

Les complications sont-elles réversibles ?

Certaines complications peuvent être gérées, mais d'autres peuvent être permanentes.
Complications Gestion des symptômes
#4

Comment les variations affectent-elles la qualité de vie ?

Elles peuvent entraîner des limitations physiques et psychologiques, affectant la qualité de vie.
Qualité de vie Limitations fonctionnelles
#5

Les complications nécessitent-elles des soins spécialisés ?

Oui, certaines complications peuvent nécessiter des soins médicaux spécialisés et un suivi.
Soins spécialisés Suivi médical

Facteurs de risque 5

#1

Quels sont les facteurs de risque des variations génétiques ?

Les antécédents familiaux, l'âge et l'environnement peuvent influencer les variations.
Facteurs de risque Antécédents familiaux
#2

L'environnement joue-t-il un rôle ?

Oui, des facteurs environnementaux peuvent interagir avec les variations génétiques.
Environnement Interactions génétiques
#3

Le mode de vie influence-t-il les variations ?

Certaines habitudes de vie, comme le tabagisme, peuvent exacerber les effets des variations.
Mode de vie Tabagisme
#4

Les facteurs socio-économiques affectent-ils les variations ?

Oui, l'accès aux soins et l'éducation peuvent influencer la gestion des variations.
Facteurs socio-économiques Accès aux soins
#5

Les variations génétiques sont-elles plus fréquentes chez certaines populations ?

Oui, certaines variations peuvent être plus courantes dans des groupes ethniques spécifiques.
Populations Variations génétiques
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apparaissent-ils à tout âge ?\nLes variations génétiques sont-elles asymptomatiques ?", "url": "https://questionsmedicales.fr/mesh/D014644#section-symptômes" }, { "@type": "MedicalWebPage", "name": "Prévention", "headline": "Prévention sur Variation génétique", "description": "Peut-on prévenir les variations génétiques ?\nQuel rôle joue le dépistage dans la prévention ?\nLes conseils génétiques aident-ils à prévenir ?\nL'alimentation influence-t-elle les variations ?\nLes vaccinations préviennent-elles des maladies génétiques ?", "url": "https://questionsmedicales.fr/mesh/D014644#section-prévention" }, { "@type": "MedicalWebPage", "name": "Traitements", "headline": "Traitements sur Variation génétique", "description": "Quels traitements existent pour les maladies génétiques ?\nLa thérapie génique est-elle efficace ?\nPeut-on prévenir les maladies par des traitements ?\nLes traitements sont-ils personnalisés ?\nQuels médicaments sont utilisés pour les variations génétiques ?", "url": "https://questionsmedicales.fr/mesh/D014644#section-traitements" }, { "@type": "MedicalWebPage", "name": "Complications", "headline": "Complications sur Variation génétique", "description": "Quelles complications peuvent survenir ?\nLes variations génétiques augmentent-elles le risque de cancer ?\nLes complications sont-elles réversibles ?\nComment les variations affectent-elles la qualité de vie ?\nLes complications nécessitent-elles des soins spécialisés ?", "url": "https://questionsmedicales.fr/mesh/D014644#section-complications" }, { "@type": "MedicalWebPage", "name": "Facteurs de risque", "headline": "Facteurs de risque sur Variation génétique", "description": "Quels sont les facteurs de risque des variations génétiques ?\nL'environnement joue-t-il un rôle ?\nLe mode de vie influence-t-il les variations ?\nLes facteurs socio-économiques affectent-ils les variations ?\nLes variations génétiques sont-elles plus fréquentes chez certaines populations ?", "url": "https://questionsmedicales.fr/mesh/D014644#section-facteurs de risque" } ] }, { "@type": "FAQPage", "mainEntity": [ { "@type": "Question", "name": "Comment détecte-t-on une variation génétique ?", "position": 1, "acceptedAnswer": { "@type": "Answer", "text": "On utilise des tests génétiques comme le séquençage de l'ADN pour identifier les variations." } }, { "@type": "Question", "name": "Quels signes indiquent une variation génétique ?", "position": 2, "acceptedAnswer": { "@type": "Answer", "text": "Des anomalies dans les résultats de tests génétiques peuvent signaler une variation." } }, { "@type": "Question", "name": "Les variations génétiques sont-elles héréditaires ?", "position": 3, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines variations peuvent être transmises de génération en génération." } }, { "@type": "Question", "name": "Quel rôle joue le génome dans le diagnostic ?", "position": 4, "acceptedAnswer": { "@type": "Answer", "text": "Le génome fournit des informations sur les variations pouvant causer des maladies." } }, { "@type": "Question", "name": "Peut-on identifier des variations par imagerie médicale ?", "position": 5, "acceptedAnswer": { "@type": "Answer", "text": "Non, l'imagerie ne détecte pas les variations génétiques, mais les effets des maladies." } }, { "@type": "Question", "name": "Quels symptômes sont liés aux variations génétiques ?", "position": 6, "acceptedAnswer": { "@type": "Answer", "text": "Les symptômes varient selon la maladie, incluant des troubles métaboliques ou neurologiques." } }, { "@type": "Question", "name": "Les variations génétiques causent-elles des maladies ?", "position": 7, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines variations peuvent être responsables de maladies héréditaires." } }, { "@type": "Question", "name": "Comment les variations affectent-elles le développement ?", "position": 8, "acceptedAnswer": { "@type": "Answer", "text": "Elles peuvent influencer le développement physique et cognitif, entraînant des retards." } }, { "@type": "Question", "name": "Les symptômes apparaissent-ils à tout âge ?", "position": 9, "acceptedAnswer": { "@type": "Answer", "text": "Pas toujours, certains symptômes peuvent se manifester à l'enfance ou à l'âge adulte." } }, { "@type": "Question", "name": "Les variations génétiques sont-elles asymptomatiques ?", "position": 10, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines variations peuvent ne pas provoquer de symptômes visibles." } }, { "@type": "Question", "name": "Peut-on prévenir les variations génétiques ?", "position": 11, "acceptedAnswer": { "@type": "Answer", "text": "Les variations génétiques sont naturelles, mais certaines maladies peuvent être évitées par des tests." } }, { "@type": "Question", "name": "Quel rôle joue le dépistage dans la prévention ?", "position": 12, "acceptedAnswer": { "@type": "Answer", "text": "Le dépistage permet d'identifier les risques et de prendre des mesures préventives." } }, { "@type": "Question", "name": "Les conseils génétiques aident-ils à prévenir ?", "position": 13, "acceptedAnswer": { "@type": "Answer", "text": "Oui, ils informent sur les risques et les options pour les familles à risque." } }, { "@type": "Question", "name": "L'alimentation influence-t-elle les variations ?", "position": 14, "acceptedAnswer": { "@type": "Answer", "text": "Une alimentation saine peut réduire le risque de maladies liées à certaines variations." } }, { "@type": "Question", "name": "Les vaccinations préviennent-elles des maladies génétiques ?", "position": 15, "acceptedAnswer": { "@type": "Answer", "text": "Non, les vaccinations ne préviennent pas les variations génétiques, mais les maladies infectieuses." } }, { "@type": "Question", "name": "Quels traitements existent pour les maladies génétiques ?", "position": 16, "acceptedAnswer": { "@type": "Answer", "text": "Les traitements incluent la thérapie génique, les médicaments et la gestion des symptômes." } }, { "@type": "Question", "name": "La thérapie génique est-elle efficace ?", "position": 17, "acceptedAnswer": { "@type": "Answer", "text": "Elle peut être efficace pour certaines maladies, mais les résultats varient selon les cas." } }, { "@type": "Question", "name": "Peut-on prévenir les maladies par des traitements ?", "position": 18, "acceptedAnswer": { "@type": "Answer", "text": "Certains traitements peuvent réduire le risque de développer des maladies génétiques." } }, { "@type": "Question", "name": "Les traitements sont-ils personnalisés ?", "position": 19, "acceptedAnswer": { "@type": "Answer", "text": "Oui, les traitements peuvent être adaptés en fonction des variations génétiques spécifiques." } }, { "@type": "Question", "name": "Quels médicaments sont utilisés pour les variations génétiques ?", "position": 20, "acceptedAnswer": { "@type": "Answer", "text": "Des médicaments spécifiques peuvent traiter les symptômes ou les causes des maladies génétiques." } }, { "@type": "Question", "name": "Quelles complications peuvent survenir ?", "position": 21, "acceptedAnswer": { "@type": "Answer", "text": "Les complications varient selon la maladie, incluant des troubles organiques ou fonctionnels." } }, { "@type": "Question", "name": "Les variations génétiques augmentent-elles le risque de cancer ?", "position": 22, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines variations génétiques sont associées à un risque accru de cancer." } }, { "@type": "Question", "name": "Les complications sont-elles réversibles ?", "position": 23, "acceptedAnswer": { "@type": "Answer", "text": "Certaines complications peuvent être gérées, mais d'autres peuvent être permanentes." } }, { "@type": "Question", "name": "Comment les variations affectent-elles la qualité de vie ?", "position": 24, "acceptedAnswer": { "@type": "Answer", "text": "Elles peuvent entraîner des limitations physiques et psychologiques, affectant la qualité de vie." } }, { "@type": "Question", "name": "Les complications nécessitent-elles des soins spécialisés ?", "position": 25, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines complications peuvent nécessiter des soins médicaux spécialisés et un suivi." } }, { "@type": "Question", "name": "Quels sont les facteurs de risque des variations génétiques ?", "position": 26, "acceptedAnswer": { "@type": "Answer", "text": "Les antécédents familiaux, l'âge et l'environnement peuvent influencer les variations." } }, { "@type": "Question", "name": "L'environnement joue-t-il un rôle ?", "position": 27, "acceptedAnswer": { "@type": "Answer", "text": "Oui, des facteurs environnementaux peuvent interagir avec les variations génétiques." } }, { "@type": "Question", "name": "Le mode de vie influence-t-il les variations ?", "position": 28, "acceptedAnswer": { "@type": "Answer", "text": "Certaines habitudes de vie, comme le tabagisme, peuvent exacerber les effets des variations." } }, { "@type": "Question", "name": "Les facteurs socio-économiques affectent-ils les variations ?", "position": 29, "acceptedAnswer": { "@type": "Answer", "text": "Oui, l'accès aux soins et l'éducation peuvent influencer la gestion des variations." } }, { "@type": "Question", "name": "Les variations génétiques sont-elles plus fréquentes chez certaines populations ?", "position": 30, "acceptedAnswer": { "@type": "Answer", "text": "Oui, certaines variations peuvent être plus courantes dans des groupes ethniques spécifiques." } } ] } ] }
Dr Olivier Menir

Contenu validé par Dr Olivier Menir

Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale


Validation scientifique effectuée le 01/08/2026

Contenu vérifié selon les dernières recommandations médicales

Sous-catégories

38 au total
└─

Hétérogénéité génétique

Genetic Heterogeneity D018740 - G05.365.331
└─

Hétéroplasmie

Heteroplasmy D000081942 - G05.365.461
└─

Mutation

Mutation D009154 - G05.365.590
└─

Variation de phase

Phase Variation D000090502 - G05.365.693
└─

Polymorphisme génétique

Polymorphism, Genetic D011110 - G05.365.795
└─

Quasi-espèce

Quasispecies D000074704 - G05.365.897
└─└─

Déséquilibre allélique

Allelic Imbalance D022981 - G05.365.590.029
└─└─

Mésappariement de bases

Base Pair Mismatch D020137 - G05.365.590.060
└─└─

Aberrations des chromosomes

Chromosome Aberrations D002869 - G05.365.590.175
└─└─

Codon non-sens

Codon, Nonsense D018389 - G05.365.590.195
└─└─

Mutation avec décalage du cadre de lecture

Frameshift Mutation D016368 - G05.365.590.265
└─└─

Mutation gain de fonction

Gain of Function Mutation D000073659 - G05.365.590.288
└─└─

Mutation germinale

Germ-Line Mutation D018095 - G05.365.590.350
└─└─

Mutation perte de fonction

Loss of Function Mutation D000073658 - G05.365.590.538
└─└─

Accumulation de mutations

Mutation Accumulation D000067552 - G05.365.590.594
└─└─

Mutation faux-sens

Mutation, Missense D020125 - G05.365.590.650
└─└─

Mutation ponctuelle

Point Mutation D017354 - G05.365.590.675
└─└─

Mutation inapparente

Silent Mutation D000069456 - G05.365.590.803
└─└─

Mutations synthétiques létales

Synthetic Lethal Mutations D000072020 - G05.365.590.917
└─└─

Variation structurale du génome

Genomic Structural Variation D056914 - G05.365.795.297
└─└─

Variants pharmacogénomiques

Pharmacogenomic Variants D000071184 - G05.365.795.446
└─└─

Polymorphisme de restriction

Polymorphism, Restriction Fragment Length D012150 - G05.365.795.595
└─└─

Polymorphisme de nucléotide simple

Polymorphism, Single Nucleotide D020641 - G05.365.795.598
└─└─

Polymorphisme de conformation simple brin

Polymorphism, Single-Stranded Conformational D018807 - G05.365.795.600
└─└─└─

Perte d'hétérozygotie

Loss of Heterozygosity D019656 - G05.365.590.029.530
└─└─└─

Caryotype anormal

Abnormal Karyotype D059786 - G05.365.590.175.024
└─└─└─

Chimérisme

Chimerism D046528 - G05.365.590.175.125
└─└─└─

Cassure de chromosome

Chromosome Breakage D019457 - G05.365.590.175.175
└─└─└─

Chromothripsis

Chromothripsis D000072837 - G05.365.590.175.310
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Isochromosomes

Isochromosomes D018404 - G05.365.590.175.430
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Micronoyaux à chromosomes défectueux

Micronuclei, Chromosome-Defective D048629 - G05.365.590.175.570
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Mosaïcisme

Mosaicism D009030 - G05.365.590.175.595
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Chromosomes en anneau

Ring Chromosomes D012303 - G05.365.590.175.760
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Aberrations des chromosomes sexuels

Sex Chromosome Aberrations D012729 - G05.365.590.175.815
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Disomie uniparentale

Uniparental Disomy D024182 - G05.365.590.175.935
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Variations de nombre de copies de segment d'ADN

DNA Copy Number Variations D056915 - G05.365.795.297.500
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Caryotype XYY

XYY Karyotype D014997 - G05.365.590.175.815.970
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Chromosome Philadelphie

Philadelphia Chromosome D010677 - G05.365.590.175.870.680

Auteurs principaux

Yoshimichi Fukuta

4 publications dans cette catégorie

Affiliations :
  • Japan International Research Center for Agricultural Sciences, Tsukuba 305-8686, Japan.
Publications dans "Variation génétique" :

Jeong-Hwa Choi

3 publications dans cette catégorie

Affiliations :
  • Department of Food Science and Nutrition, Keimyung University, Daegu42601, Republic of Korea.
Publications dans "Variation génétique" :

Angelos Koutras

2 publications dans cette catégorie

Affiliations :
  • Division of Oncology, Department of Medicine, University of Patras, Patras, Greece.
Publications dans "Variation génétique" :

Paula Soria-Chacartegui

2 publications dans cette catégorie

Affiliations :
  • Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :

Dolores Ochoa

2 publications dans cette catégorie

Affiliations :
  • Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :

Manuel Román

2 publications dans cette catégorie

Affiliations :
  • Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :

Gina Mejía-Abril

2 publications dans cette catégorie

Affiliations :
  • Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
Publications dans "Variation génétique" :

Francisco Abad-Santos

2 publications dans cette catégorie

Affiliations :
  • Clinical Pharmacology Department, Hospital Universitario de La Princesa, Instituto Teófilo Hernando, Instituto de Investigación Sanitaria La Princesa (IP), Universidad Autónoma de Madrid (UAM), 28006 Madrid, Spain.
  • Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Publications dans "Variation génétique" :

Georgia-Angeliki Koliou

2 publications dans cette catégorie

Affiliations :
  • Section of Biostatistics, Hellenic Cooperative Oncology Group, Data Office, Athens, Greece.
Publications dans "Variation génétique" :

Foteinos-Ioannis Dimitrakopoulos

2 publications dans cette catégorie

Affiliations :
  • Division of Oncology, Department of Medicine, University Hospital, Medical School, University of Patras, Patras, Greece.
Publications dans "Variation génétique" :

Kyriaki Papadopoulou

2 publications dans cette catégorie

Affiliations :
  • Laboratory of Molecular Oncology, Hellenic Foundation for Cancer Research/Aristotle University of Thessaloniki, Thessaloniki, Greece.
Publications dans "Variation génétique" :

Anastasios Visvikis

2 publications dans cette catégorie

Affiliations :
  • Third Department of Medical Oncology, Agii Anargiri Cancer Hospital, Athens, Greece.
Publications dans "Variation génétique" :

George Fountzilas

2 publications dans cette catégorie

Affiliations :
  • Laboratory of Molecular Oncology, Hellenic Foundation for Cancer Research/Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • German Oncology Center, Limassol, Cyprus.
Publications dans "Variation génétique" :

Matthew Traylor

2 publications dans cette catégorie

Affiliations :
  • From the Department of Clinical Neurosciences, Stroke Research Group (M.T., D.J.T., I.D.C., D.M.L.F., A.O.O., L.R.-J., H.S.M.), University of Cambridge, UK; Department of Cerebrovascular Diseases (G.B.), Fondazione IRCCS Istituto Neurologico "Carlo Besta," Milan, Italy; Institute for Stroke and Dementia Research (M.D.), Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich; German Center for Neurodegenerative Diseases (DZNE) and Munich Cluster for Systems Neurology (SyNergy) (M.D.), Germany; Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) (R.L.), KU Leuven-University of Leuven; Department of Neurology (R.L.), University Hospitals Leuven; Laboratory of Neurobiology (R.L.), VIB Center for Brain and Disease Research, Leuven, Belgium; Center for Human Genetic Research (J.R.) and Division of Neurocritical Care and Emergency Neurology (J.R.) and J. Philip Kistler Stroke Research Center (J.R., N.S.R.), Department of Neurology, Massachusetts General Hospital, Boston; Nuffield Department of Clinical Neurosciences (Clinical Neurology), Stroke Prevention Research Unit (P.M.R.), University of Oxford; Centre for Clinical Brain Sciences and Institute for Genetics and Molecular Medicine (C.L.M.S.), University of Edinburgh, UK; Stroke Division, Florey Institute of Neuroscience and Mental Health (V.T.), University of Melbourne; and Department of Neurology (V.T.), Austin Health, Heidelberg, Victoria, Australia. MT628@medschl.cam.ac.uk.
Publications dans "Variation génétique" :

Martin Dichgans

2 publications dans cette catégorie

Affiliations :
  • From the Department of Clinical Neurosciences, Stroke Research Group (M.T., D.J.T., I.D.C., D.M.L.F., A.O.O., L.R.-J., H.S.M.), University of Cambridge, UK; Department of Cerebrovascular Diseases (G.B.), Fondazione IRCCS Istituto Neurologico "Carlo Besta," Milan, Italy; Institute for Stroke and Dementia Research (M.D.), Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich; German Center for Neurodegenerative Diseases (DZNE) and Munich Cluster for Systems Neurology (SyNergy) (M.D.), Germany; Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) (R.L.), KU Leuven-University of Leuven; Department of Neurology (R.L.), University Hospitals Leuven; Laboratory of Neurobiology (R.L.), VIB Center for Brain and Disease Research, Leuven, Belgium; Center for Human Genetic Research (J.R.) and Division of Neurocritical Care and Emergency Neurology (J.R.) and J. Philip Kistler Stroke Research Center (J.R., N.S.R.), Department of Neurology, Massachusetts General Hospital, Boston; Nuffield Department of Clinical Neurosciences (Clinical Neurology), Stroke Prevention Research Unit (P.M.R.), University of Oxford; Centre for Clinical Brain Sciences and Institute for Genetics and Molecular Medicine (C.L.M.S.), University of Edinburgh, UK; Stroke Division, Florey Institute of Neuroscience and Mental Health (V.T.), University of Melbourne; and Department of Neurology (V.T.), Austin Health, Heidelberg, Victoria, Australia.
Publications dans "Variation génétique" :

Hugh S Markus

2 publications dans cette catégorie

Affiliations :
  • From the Department of Clinical Neurosciences, Stroke Research Group (M.T., D.J.T., I.D.C., D.M.L.F., A.O.O., L.R.-J., H.S.M.), University of Cambridge, UK; Department of Cerebrovascular Diseases (G.B.), Fondazione IRCCS Istituto Neurologico "Carlo Besta," Milan, Italy; Institute for Stroke and Dementia Research (M.D.), Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich; German Center for Neurodegenerative Diseases (DZNE) and Munich Cluster for Systems Neurology (SyNergy) (M.D.), Germany; Department of Neurosciences, Experimental Neurology and Leuven Research Institute for Neuroscience and Disease (LIND) (R.L.), KU Leuven-University of Leuven; Department of Neurology (R.L.), University Hospitals Leuven; Laboratory of Neurobiology (R.L.), VIB Center for Brain and Disease Research, Leuven, Belgium; Center for Human Genetic Research (J.R.) and Division of Neurocritical Care and Emergency Neurology (J.R.) and J. Philip Kistler Stroke Research Center (J.R., N.S.R.), Department of Neurology, Massachusetts General Hospital, Boston; Nuffield Department of Clinical Neurosciences (Clinical Neurology), Stroke Prevention Research Unit (P.M.R.), University of Oxford; Centre for Clinical Brain Sciences and Institute for Genetics and Molecular Medicine (C.L.M.S.), University of Edinburgh, UK; Stroke Division, Florey Institute of Neuroscience and Mental Health (V.T.), University of Melbourne; and Department of Neurology (V.T.), Austin Health, Heidelberg, Victoria, Australia.
Publications dans "Variation génétique" :

None None

2 publications dans cette catégorie

Publications dans "Variation génétique" :

Ahmed M Sallam

2 publications dans cette catégorie

Affiliations :
  • Animal and Poultry Production Division, Desert Research Center, 11753, Mataryia, Egypt.
Publications dans "Variation génétique" :

Gong Cheng

2 publications dans cette catégorie

Affiliations :
  • College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Publications dans "Variation génétique" :

Andre Franke

2 publications dans cette catégorie

Affiliations :
  • Institute of Clinical Molecular Biology, Kiel University, 24118 Kiel, Germany.
Publications dans "Variation génétique" :

Sources (10000 au total)

Understanding genetic variations associated with familial breast cancer.

Breast cancer is the most frequent cancer among women. Genetics are the main risk factor for breast cancer. Statistics show that 15-25% of breast cancers are inherited among those with cancer-prone re... A search of the PubMed database was carried out spanning from 2005 to July 2024, yielding a total of 768 articles that delve into the realm of familial breast cancer, concerning genes and genetic synd... We report on a set of 20 familial breast cancer -associated genes into high, moderate, and low penetrance levels. Additionally, 10 genetic disorders were found to be linked with familial breast cancer... Familial breast cancer has been linked to several genetic diseases and mutations, according to studies. Screening for genetic disorders is recommended by National Comprehensive Cancer Network recommen...

Genetic variation and genetic complexity of nodule occupancy in soybean inoculated with USDA110 and USDA123 rhizobium strains.

Symbiotic nitrogen fixation differs among Bradyrhizobium japonicum strains. Soybean inoculated with USDA123 has a lower yield than strains known to have high nitrogen fixation efficiency, such as USDA... Seventy-three G. max accessions with significantly different nodule number of USDA110 and USDA123 were identified. After double inoculating 35 of the 73 accessions, it was observed that PI189939, PI31... High-throughput phenotyping systems to characterize nodule number and occupancy were developed, and soybean germplasm restricting rhizobium strain USDA123 but preferring USDA110 was identified. The la...