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W Scherer

Showing results (681-690 of 915) with videos related to

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JAMA Neurology|September 27, 2021
Effect of Methylphenidate on Apathy in Patients With Alzheimer Disease: The ADMET 2 Randomized Clinical TrialJacobo Mintzer, Krista L Lanctôt, Roberta W Scherer, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Nature Communications|August 8, 2019
Haploinsufficiency in the ANKS1B gene encoding AIDA-1 leads to a neurodevelopmental syndromeAbigail U Carbonell, Chang Hoon Cho, Jaafar O Tindi, et al.
Plos Genetics|May 8, 2007
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolutionLayla Parker-Katiraee, Andrew R Carson, Takahiro Yamada, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
BMJ (Clinical Research Ed.)|April 24, 2023
CONSORT Harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomised trialsDaniela R Junqueira, Liliane Zorzela, Susan Golder, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|June 23, 2020
Measuring Apathy in Alzheimer's Disease in the Apathy in Dementia Methylphenidate Trial 2 (ADMET 2): A Comparison of InstrumentsKrista L Lanctôt, Roberta W Scherer, Abby Li, et al.
Nature|September 6, 2000
Colorectal carcinomas in mice lacking the catalytic subunit of PI(3)KgammaT Sasaki, J Irie-Sasaki, Y Horie, et al.
Science (New York, N.Y.)|February 10, 2007
Relative impact of nucleotide and copy number variation on gene expression phenotypesBarbara E Stranger, Matthew S Forrest, Mark Dunning, et al.
Pageof 92

Showing results (681-690 of 915) with videos related to

Sort By:
Pageof 92
JAMA Neurology|September 27, 2021
Effect of Methylphenidate on Apathy in Patients With Alzheimer Disease: The ADMET 2 Randomized Clinical TrialJacobo Mintzer, Krista L Lanctôt, Roberta W Scherer, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Nature Communications|August 8, 2019
Haploinsufficiency in the ANKS1B gene encoding AIDA-1 leads to a neurodevelopmental syndromeAbigail U Carbonell, Chang Hoon Cho, Jaafar O Tindi, et al.
Plos Genetics|May 8, 2007
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolutionLayla Parker-Katiraee, Andrew R Carson, Takahiro Yamada, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersSiddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, et al.
BMJ (Clinical Research Ed.)|April 24, 2023
CONSORT Harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomised trialsDaniela R Junqueira, Liliane Zorzela, Susan Golder, et al.
Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|June 23, 2020
Measuring Apathy in Alzheimer's Disease in the Apathy in Dementia Methylphenidate Trial 2 (ADMET 2): A Comparison of InstrumentsKrista L Lanctôt, Roberta W Scherer, Abby Li, et al.
Nature|September 6, 2000
Colorectal carcinomas in mice lacking the catalytic subunit of PI(3)KgammaT Sasaki, J Irie-Sasaki, Y Horie, et al.
Science (New York, N.Y.)|February 10, 2007
Relative impact of nucleotide and copy number variation on gene expression phenotypesBarbara E Stranger, Matthew S Forrest, Mark Dunning, et al.
Pageof 92