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Physical Review Letters
|
June 13, 2020
Halo Structure of the Neutron-Dripline Nucleus ^{19}B
K J Cook, T Nakamura, Y Kondo, et al.
BMJ Open
|
June 4, 2024
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry
Madeleine Bloomfield, Alexandra Lautarescu, Síofra Heraty, et al.
NPJ Genomic Medicine
|
July 10, 2019
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Plos Genetics
|
February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
Claire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics
|
September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments
Claire S Leblond, Caroline Nava, Anne Polge, et al.
NPJ Genomic Medicine
|
December 22, 2017
A framework to identify contributing genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Physical Review Letters
|
December 10, 2023
Validation of the ^{10}Be Ground-State Molecular Structure Using ^{10}Be(p,pα)^{6}He Triple Differential Reaction Cross-Section Measurements
P J Li, D Beaumel, J Lee, et al.
Nature Communications
|
April 16, 2016
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
Kelly L Williams, Simon Topp, Shu Yang, et al.
Neuron
|
November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
Bradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Physical Review Letters
|
January 12, 2024
High-Precision Spectroscopy of ^{20}O Benchmarking Ab Initio Calculations in Light Nuclei
I Zanon, E Clément, A Goasduff, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 72) with videos related to
Sort By:
Page
of 8
Physical Review Letters
|
June 13, 2020
Halo Structure of the Neutron-Dripline Nucleus ^{19}B
K J Cook, T Nakamura, Y Kondo, et al.
BMJ Open
|
June 4, 2024
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry
Madeleine Bloomfield, Alexandra Lautarescu, Síofra Heraty, et al.
NPJ Genomic Medicine
|
July 10, 2019
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Plos Genetics
|
February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
Claire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics
|
September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments
Claire S Leblond, Caroline Nava, Anne Polge, et al.
NPJ Genomic Medicine
|
December 22, 2017
A framework to identify contributing genes in patients with Phelan-McDermid syndrome
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Physical Review Letters
|
December 10, 2023
Validation of the ^{10}Be Ground-State Molecular Structure Using ^{10}Be(p,pα)^{6}He Triple Differential Reaction Cross-Section Measurements
P J Li, D Beaumel, J Lee, et al.
Nature Communications
|
April 16, 2016
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
Kelly L Williams, Simon Topp, Shu Yang, et al.
Neuron
|
November 7, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
Bradley N Smith, Nicola Ticozzi, Claudia Fallini, et al.
Physical Review Letters
|
January 12, 2024
High-Precision Spectroscopy of ^{20}O Benchmarking Ab Initio Calculations in Light Nuclei
I Zanon, E Clément, A Goasduff, et al.
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of 8