Visualitzant R - Articles científics per títol

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey

Vermunicht, Paulien; Grecu, Mihaela; Buckley, Claire M.; Pala Vila, Elena; Mairesse, Georges H.; Deharo, Jean-Claude (Frontiers Media, 2023-02-15)

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients

Machuca, Candela; Correa Vela, Marta; García-Navas, Deyanira; Darling, Alejandra; Villalón-García, Irene; Sánchez-Alcázar, José Antonio; Perez Dueñas, Belen (Elsevier, 2021-05)

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Arias-Salgado, Elena G.; Galvez, Eva; Planas-Cerezales, Lurdes; Pintado-Berninches, Laura; Vallespin, Elena; Martinez, Pilar; Martín Nalda, Andrea; Díaz de Heredia Rubio, Maria Cristina; Martínez Gallo, Mónica; Uria Oficialdegui, Maria Luz (BMC, 2019-04-17)

Genetic association study of childhood aggression across raters, instruments, and age

Ip, Hill F.; van der Laan, Camiel M.; Krapohl, Eva M. L.; Brikell, Isabell; Sanchez Mora, Cristina P; Nolte, Ilja M.; Soler Artigas, Maria; Rovira Lorente, Paula; Bosch Munso, Rosa M; Español Martín, Gemma; Ramos Quiroga, José Antonio; Casas Brugué, Miquel; Ribases Haro, Marta (Springer Nature, 2021-07-30)

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome

Sahi, Nitin; Haider, Lukas; Chung, Karen; Kanber, Baris; Samson, Rebecca; Tur Gomez, Carmen; Prados Carrasco, Ferran (Oxford University Press, 2023)

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Martinez de LaPiscina Martin, Idoia; Kouri, Chrysanthi; Aurrekoetxea, Josu; Sanchez, Mirian; Naamneh Elzenaty, Rawda; Sauter, Kay-Sara; Camats Tarruella, Núria (Public Library of Science, 2023-07-11)

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Harder, Aster V. E.; Winsvold, Bendik S.; Noordam, Raymond; Vijfhuizen, Lisanne S.; Børte, Sigrid; Kogelman, Lisette J. A.; Pozo Rosich, Patricia (MDPI, 2021-08)

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients

López‑Cotarelo, Pilar; González‑Jiménez, Adela; Agudo‑Jiménez, Teresa; Abarca Zabalía, Judith; Pilo, Belén; Comabella Lopez, Manuel; Aladro, Yolanda (Nature Research, 2021-11-01)

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations

Farinango, Camila; Gallardo-Cóndor, Jennifer; Freire Paspuel, Byron; Flores-Espinoza, Rodrigo; Jaramillo-Koupermann, Gabriela; López-Cortés, Andrés (MDPI, 2022-06-10)

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease

Sáez, M. E.; González-Pérez, A.; Hernández-Olasagarre, B.; Beà, Aida; Moreno-Grau, S.; de Rojas, Itziar; Comella Carnice, Joan X. (Nature Publishing Group, 2019-11-13)

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment

Maisterra Santos, Olga; Jimenez Balado, Joan; Carrera, Caty; Torres‑Aguila, Nuria P.; Muiño, Elena; Cullell, Natalia (Nature Research, 2021-03-25)

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells

Mena, Jorge; Alloza, Iraide; Tulloch Navarro, Raquel; Aldekoa, Ane; Díez García, Javier; Villanueva Etxebarria, Ane; Midaglia Fernandez, Luciana; Montalban Gairín, Xavier; Comabella Lopez, Manuel; Malhotra Sareen, Sunny (Frontiers Media, 2022-01)

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool

Villafranca Magdalena, Beatriz; Masferrer Ferragutcasas, Carina; Lopez Gil, Carlos; Coll De la Rubia, Eva; Rebull Santamaria, Marta; Parra, Genis; García Jiménez, Angel; Cabrera Diaz, Silvia; Colas Ortega, Eva; Gil Moreno, Antonio; Moiola, Cristian Pablo; Reques Llanos, Armando (MDPI, 2022-06-03)

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

Duperron, Marie-Gabrielle; Knol, Maria; Le Grand, Quentin; Evans, Tavia; Mishra, Aniket; Tsuchida, Ami; Delgado Martínez, Maria Pilar (Springer Nature, 2023-04)

Gestational age-based reference ranges for cervical length and preterm birth prediction in triplet pregnancies: an observational retrospective study

Rodó Rodríguez, Carlota; de la Calle, María; Maroto, Anna; Maiz Elizaran, Nerea; García Manau, Pablo; Mendoza Cobaleda, Manel; Bartha, Jose Luis; Carreras Moratonas, Elena; Arévalo Martínez, Silvia (BMC, 2022-08-30)

GH/IGF-1 Abnormalities and Muscle Impairment: From Basic Research to Clinical Practice

Biagetti Biagetti, Betina; Simó Canonge, Rafael (MDPI, 2021-01-02)

Glial cell alterations in diabetes-induced neurodegeneration

Cabeza Fernández, Sonia; Gomez-Sanchez, Jose A.; de la Fuente, Alerie Guzman; Llorián-Salvador, María (Springer, 2024-01-18)

Glioblastoma Pseudoprogression Discrimination Using Multiparametric Magnetic Resonance Imaging, Principal Component Analysis, and Supervised and Unsupervised Machine Learning

Thenier-Villa, Jose Luis; Martinez-Ricarte, Fran; Figueroa Vezirián, Margarita; Arikan Abello, Fuat (Elsevier, 2024-03)

Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function

Mortlock, Sally-Anne; Houshdaran, Sahar; Kosti, Idit; RAHMIOGLU, NILUFER; Nezhat, Camran; Vitonis, Allison ; Santamaria, Xavier (Nature Portfolio, 2023-08-16)

GLP-1 Receptor Agonists in Diabetic Kidney Disease: From Physiology to Clinical Outcomes

Rojano Toimil, Alba; Ciudin Mihai, Andreea (MDPI, 2021-09)

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Visualitzant VHIR - Articles científics per títol

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Genetic association study of childhood aggression across raters, instruments, and age

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

Gestational age-based reference ranges for cervical length and preterm birth prediction in triplet pregnancies: an observational retrospective study

GH/IGF-1 Abnormalities and Muscle Impairment: From Basic Research to Clinical Practice

Glial cell alterations in diabetes-induced neurodegeneration

Glioblastoma Pseudoprogression Discrimination Using Multiparametric Magnetic Resonance Imaging, Principal Component Analysis, and Supervised and Unsupervised Machine Learning

Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function

GLP-1 Receptor Agonists in Diabetic Kidney Disease: From Physiology to Clinical Outcomes

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Visualitzant VHIR - Articles científics per títol

General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey ﻿

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients ﻿

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes ﻿

Genetic association study of childhood aggression across raters, instruments, and age ﻿

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome ﻿

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations ﻿

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache ﻿

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients ﻿

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations ﻿

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease ﻿

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment ﻿

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells ﻿

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool ﻿

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease ﻿

Gestational age-based reference ranges for cervical length and preterm birth prediction in triplet pregnancies: an observational retrospective study ﻿

GH/IGF-1 Abnormalities and Muscle Impairment: From Basic Research to Clinical Practice ﻿

Glial cell alterations in diabetes-induced neurodegeneration ﻿

Glioblastoma Pseudoprogression Discrimination Using Multiparametric Magnetic Resonance Imaging, Principal Component Analysis, and Supervised and Unsupervised Machine Learning ﻿

Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function ﻿

GLP-1 Receptor Agonists in Diabetic Kidney Disease: From Physiology to Clinical Outcomes ﻿

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General practitioners’ perceptions on opportunistic single-time point screening for atrial fibrillation: A European quantitative survey

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients

Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

Genetic association study of childhood aggression across raters, instruments, and age

Genetic influences on disease course and severity, 30 years after a clinically isolated syndrome

Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations

Genetic Susceptibility Loci in Genomewide Association Study of Cluster Headache

Genetic variation in NDFIP1 modifies the metabolic patterns in immune cells of multiple sclerosis patients

Genetic Variations of the DPYD Gene and Its Relationship with Ancestry Proportions in Different Ecuadorian Trihybrid Populations

Genome Wide Meta-Analysis identifies common genetic signatures shared by heart function and Alzheimer’s disease

Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment

Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55–IL6ST Gene Region in Immature Dendritic Cells

Genomic Validation of Endometrial Cancer Patient-Derived Xenograft Models as a Preclinical Tool

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

Gestational age-based reference ranges for cervical length and preterm birth prediction in triplet pregnancies: an observational retrospective study

GH/IGF-1 Abnormalities and Muscle Impairment: From Basic Research to Clinical Practice

Glial cell alterations in diabetes-induced neurodegeneration

Glioblastoma Pseudoprogression Discrimination Using Multiparametric Magnetic Resonance Imaging, Principal Component Analysis, and Supervised and Unsupervised Machine Learning

Global endometrial DNA methylation analysis reveals insights into mQTL regulation and associated endometriosis disease risk and endometrial function

GLP-1 Receptor Agonists in Diabetic Kidney Disease: From Physiology to Clinical Outcomes