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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
October 25, 2025
Cardiovascular disease as a mediator in the relationship between lifestyle risk factors and cognitive outcomes: a scoping review
Abby L J Hensel, Therese Chan, Raisa Ahmed, et al.
European Journal of Human Genetics : EJHG
|
July 4, 2024
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes
Noor Smal, Fatma Majdoub, Katrien Janssens, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 30, 2014
The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism
Geert Vandeweyer, Céline Helsmoortel, Anke Van Dijck, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
September 9, 1999
Interlaboratory comparison of ultrasonic backscatter, attenuation, and speed measurements
E L Madsen, F Dong, G R Frank, et al.
Clinical Lymphoma, Myeloma & Leukemia
|
November 29, 2021
Comparison of Cilta-cel, an Anti-BCMA CAR-T Cell Therapy, Versus Conventional Treatment in Patients With Relapsed/Refractory Multiple Myeloma
Luciano J Costa, Yi Lin, R Frank Cornell, et al.
Neurobiology of Aging
|
October 24, 2007
Prominent phenotypic variability associated with mutations in Progranulin
Brendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Nature Medicine
|
May 14, 2024
Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals
Alexander J M Dingemans, Sandra Jansen, Jeroen van Reeuwijk, et al.
Human Molecular Genetics
|
May 26, 2019
Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15
Hanyin Cheng, Leah Gottlieb, Elaine Marchi, et al.
Human Molecular Genetics
|
February 8, 2013
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders
Zafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
Ebiomedicine
|
May 28, 2026
An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice
Claudio Peter D'Incal, Elisa Cappuyns, Flora Paldi, et al.
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of 136
Search research articles
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Showing results (1311-1320 of 1,358) with videos related to
Sort By:
Page
of 136
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
October 25, 2025
Cardiovascular disease as a mediator in the relationship between lifestyle risk factors and cognitive outcomes: a scoping review
Abby L J Hensel, Therese Chan, Raisa Ahmed, et al.
European Journal of Human Genetics : EJHG
|
July 4, 2024
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes
Noor Smal, Fatma Majdoub, Katrien Janssens, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 30, 2014
The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism
Geert Vandeweyer, Céline Helsmoortel, Anke Van Dijck, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
September 9, 1999
Interlaboratory comparison of ultrasonic backscatter, attenuation, and speed measurements
E L Madsen, F Dong, G R Frank, et al.
Clinical Lymphoma, Myeloma & Leukemia
|
November 29, 2021
Comparison of Cilta-cel, an Anti-BCMA CAR-T Cell Therapy, Versus Conventional Treatment in Patients With Relapsed/Refractory Multiple Myeloma
Luciano J Costa, Yi Lin, R Frank Cornell, et al.
Neurobiology of Aging
|
October 24, 2007
Prominent phenotypic variability associated with mutations in Progranulin
Brendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Nature Medicine
|
May 14, 2024
Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals
Alexander J M Dingemans, Sandra Jansen, Jeroen van Reeuwijk, et al.
Human Molecular Genetics
|
May 26, 2019
Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15
Hanyin Cheng, Leah Gottlieb, Elaine Marchi, et al.
Human Molecular Genetics
|
February 8, 2013
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders
Zafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
Ebiomedicine
|
May 28, 2026
An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice
Claudio Peter D'Incal, Elisa Cappuyns, Flora Paldi, et al.
Page
of 136