Visualitzant l d'Hebron Institut de Recerca

Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature

van der Laan, Liselot; Rooney, Kathleen; Haghshenas, Sadegheh; Silva, Ananilia; McConkey, Haley; Relator, Raissa; Lasa-Aranzasti, Amaia; Castells Sarret, Neus; Valenzuela, Irene; Trujillano Lidón, Laura; Campos Estela, Berta (MDPI, 2023-09-18)

Functional rare variants influence the clinical response to anti-TNF therapy in Crohn’s disease

Aterido Ballonga, Adria; Guerra, Iván; Cabriada, Jose Luis; Marsal Barril, Sara; Julia Cano, Antonio; Chaparro, María; Bujanda, Luis; Iborra, Marisa (SAGE Publications, 2019-09-25)

Functional Recovery and Serum Angiogenin Changes According to Intensity of Rehabilitation Therapy After Stroke

Garcia Rodriguez, Nicolas; Rodriguez Gonzalez, Susana; Ignacio Tejada, Pedro; Miranda-Artieda, Zuberoa Maite; Ridao, Natalia; Buxo Masip, Xavier; Perez-Mesquida, Maria Engracia; Perez Bazan, Laura Mónica; Quintana Luque, Manuel; Olive Gadea, Marta; Penalba Morenilla, Anna; Rosell Novel, Anna; Inzitari, Marco (Frontiers Media, 2021-11)

Functioning assessment short test (FAST): validity and reliability in adults with Autism Spectrum Disorder

Gisbert Gustemps, Laura; Lugo Marin, Jorge; Español Martín, Gemma; Bonnín, C. Mar; Ramos Quiroga, José Antonio; Vieta, Eduard; Setien Ramos, Imanol (BMC, 2021-06-29)

Fungal and Bacterial Loads: Noninvasive Inflammatory Bowel Disease Biomarkers for the Clinical Setting

Philippe Sarrabayrouse, Guillaume; Elias Vidal, Andrea; Yañez Araya, Francisca; Mayorga Ayala, Luis Fernando; Bartoli, Chiara; Casellas Jordá, Francesc; Borruel Sainz, Natalia; Herrera de Guise, Claudia Maria; Manichanh, Chaysavanh; Varela Castro, Encarna (American Society for Microbiology, 2021-03)

FunOMIC: Pipeline with built-in fungal taxonomic and functional databases for human mycobiome profiling

Manichanh, Chaysavanh; Xie, Zixuan (Elsevier, 2022)

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Gracia-Diaz, Carolina; Zhou, Yijing; Yang, Qian; Maroofian, Reza; España, Paula; Lee, Chul-Hwan; Padilla Sirera, Natàlia (Nature Portfolio, 2023-07-11)

Gait analysis under the lens of statistical physics

Zanin, Massimiliano; Olivares, Felipe; Pulido-Valdeolivas, Irene; Rausell Tamayo, Estrella; Gómez Andrés, David (Elsevier, 2022)

Gait Assessment in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Alemañ Díez, Jose; López Diego, Verónica; Salvadó Figueras, Maria; Llaurado, Arnau; Quintana, Manuel; Gratacòs-Viñola, Margarida; Vidal-Taboada, jose M; Restrepo Vera, Juan Luis; Sánchez-Tejerina, Daniel; Sotoca, Javier; Raguer, Núria; Juntas Morales, Raúl (WileyHindawi, 2024-04-08)

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis

Pozo Rosich, Patricia; Samaan, Karen; Schwedt, Todd J.; Nicholson, Robert A.; Rettiganti, Mallikarjuna; Pearlman, Eric M. (Springer, 2021-06)

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells

Bellio, Chiara; Emperador, Marta; Castellano Escuder, Pol; Gris Oliver, Albert; Canals Suris, Francesc; Sánchez Pla, Alex; Serra, Violeta; Zamora, Esther; Arribas, Joaquin; Saura, Cristina; Tabernero, Josep; Villanueva Cardús, Josep (MDPI, 2022-05-23)

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy

Kagiava, Alexia; Karaiskos, Christos; Lapathitis, George; Heslegrave, Amanda; Sargiannidou, Irene; Zetterberg, Henrik; Bosch, Assumpció (Cell Press, 2023-09-14)

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice

Mòdol-Caballero, Guillem; Herrando-Grabulosa, Mireia; Verdés Franquesa, Sergi; García-Lareu, Belén; Hernández, Neus; Francos-Quijorna, Isaac; Bosch Merino, Assumpció (Frontiers Media, 2021-09-22)

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)

Scientia. Dipòsit d'Informació Digital del Departament de Salut

Visualitzant Vall d'Hebron Institut de Recerca - VHIR per títol

Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature

Functional rare variants influence the clinical response to anti-TNF therapy in Crohn’s disease

Functional Recovery and Serum Angiogenin Changes According to Intensity of Rehabilitation Therapy After Stroke

Functioning assessment short test (FAST): validity and reliability in adults with Autism Spectrum Disorder

Fungal and Bacterial Loads: Noninvasive Inflammatory Bowel Disease Biomarkers for the Clinical Setting

FunOMIC: Pipeline with built-in fungal taxonomic and functional databases for human mycobiome profiling

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Gait analysis under the lens of statistical physics

Gait Assessment in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice

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

Coneix Scientia

Guies i ajudes

Directe a...

Coneix Scientia

Guies i ajudes

Directe a...

Visualitzant Vall d'Hebron Institut de Recerca - VHIR per títol

Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature ﻿

Functional rare variants influence the clinical response to anti-TNF therapy in Crohn’s disease ﻿

Functional Recovery and Serum Angiogenin Changes According to Intensity of Rehabilitation Therapy After Stroke ﻿

Functioning assessment short test (FAST): validity and reliability in adults with Autism Spectrum Disorder ﻿

Fungal and Bacterial Loads: Noninvasive Inflammatory Bowel Disease Biomarkers for the Clinical Setting ﻿

FunOMIC: Pipeline with built-in fungal taxonomic and functional databases for human mycobiome profiling ﻿

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders ﻿

Gait analysis under the lens of statistical physics ﻿

Gait Assessment in Chronic Inflammatory Demyelinating Polyradiculoneuropathy ﻿

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis ﻿

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells ﻿

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy ﻿

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice ﻿

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 ﻿

Coneix Scientia

Guies i ajudes

Directe a...

Coneix Scientia

Guies i ajudes

Directe a...

Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature

Functional rare variants influence the clinical response to anti-TNF therapy in Crohn’s disease

Functional Recovery and Serum Angiogenin Changes According to Intensity of Rehabilitation Therapy After Stroke

Functioning assessment short test (FAST): validity and reliability in adults with Autism Spectrum Disorder

Fungal and Bacterial Loads: Noninvasive Inflammatory Bowel Disease Biomarkers for the Clinical Setting

FunOMIC: Pipeline with built-in fungal taxonomic and functional databases for human mycobiome profiling

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders

Gait analysis under the lens of statistical physics

Gait Assessment in Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Galcanezumab Provides Consistent Efficacy Throughout the Dosing Interval Among Patients with Episodic and Chronic Migraine: A Post Hoc Analysis

GDF15 Is an Eribulin Response Biomarker also Required for Survival of DTP Breast Cancer Cells

Gene replacement therapy in two Golgi-retained CMT1X mutants before and after the onset of demyelinating neuropathy

Gene Therapy Overexpressing Neuregulin 1 Type I in Combination With Neuregulin 1 Type III Promotes Functional Improvement in the SOD1G93A ALS Mice

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