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March 30, 2023
The Genetic and Epigenetic Features of Bilateral Wilms Tumor Predisposition: A Report from the Children's Oncology Group AREN18B5-Q Study
Andrew J Murphy, Changde Cheng, Justin Williams, et al.
Nature Communications
|
December 18, 2023
Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q
Andrew J Murphy, Changde Cheng, Justin Williams, et al.
JAMA
|
May 17, 2022
Ethical Considerations for the Inclusion of Patient-Reported Outcomes in Clinical Research: The PRO Ethics Guidelines
Samantha Cruz Rivera, Olalekan Lee Aiyegbusi, Jonathan Ives, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2023
Vertebral Body Reshaping after Fractures: An Important Index of Recovery in Glucocorticoid-Treated Children
Jinhui Ma, Kerry Siminoski, Jacob L Jaremko, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
August 14, 2021
Investigation of gene-environment interactions in relation to tic severity
Mohamed Abdulkadir, Dongmei Yu, Lisa Osiecki, et al.
European Archives of Psychiatry and Clinical Neuroscience
|
May 31, 2017
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach
Mohamed Abdulkadir, Douglas Londono, Derek Gordon, et al.
Journal of Psychiatric Research
|
August 6, 2016
Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder
Mohamed Abdulkadir, Jay A Tischfield, Robert A King, et al.
JAMA Oncology
|
October 7, 2021
Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes
Catherine Goudie, Leora Witkowski, Noelle Cullinan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders
Belinda Wang, Matthew N Tran, Sheng Wang, et al.
Neuron
|
June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
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of 60
Search research articles
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Showing results (491-500 of 597) with videos related to
Sort By:
Page
of 60
Research Square
|
March 30, 2023
The Genetic and Epigenetic Features of Bilateral Wilms Tumor Predisposition: A Report from the Children's Oncology Group AREN18B5-Q Study
Andrew J Murphy, Changde Cheng, Justin Williams, et al.
Nature Communications
|
December 18, 2023
Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q
Andrew J Murphy, Changde Cheng, Justin Williams, et al.
JAMA
|
May 17, 2022
Ethical Considerations for the Inclusion of Patient-Reported Outcomes in Clinical Research: The PRO Ethics Guidelines
Samantha Cruz Rivera, Olalekan Lee Aiyegbusi, Jonathan Ives, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2023
Vertebral Body Reshaping after Fractures: An Important Index of Recovery in Glucocorticoid-Treated Children
Jinhui Ma, Kerry Siminoski, Jacob L Jaremko, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
August 14, 2021
Investigation of gene-environment interactions in relation to tic severity
Mohamed Abdulkadir, Dongmei Yu, Lisa Osiecki, et al.
European Archives of Psychiatry and Clinical Neuroscience
|
May 31, 2017
Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach
Mohamed Abdulkadir, Douglas Londono, Derek Gordon, et al.
Journal of Psychiatric Research
|
August 6, 2016
Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder
Mohamed Abdulkadir, Jay A Tischfield, Robert A King, et al.
JAMA Oncology
|
October 7, 2021
Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes
Catherine Goudie, Leora Witkowski, Noelle Cullinan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders
Belinda Wang, Matthew N Tran, Sheng Wang, et al.
Neuron
|
June 11, 2011
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, et al.
Page
of 60