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Authors: Adam J de Smith
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Journal Article
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus
Jon Foss-Skiftesvik and others
Neuro-Oncology, Volume 25, Issue 9, September 2023, Pages 1709–1720, https://doi.org/10.1093/neuonc/noad042
Published: 22 February 2023
Journal Article
Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men
Anqi Wang and others
Human Molecular Genetics, Volume 32, Issue 3, 1 February 2023, Pages 489–495, https://doi.org/10.1093/hmg/ddac214
Published: 26 August 2022
Journal Article
Investigating DNA methylation as a mediator of genetic risk in childhood acute lymphoblastic leukemia
Keren Xu and others
Human Molecular Genetics, Volume 31, Issue 21, 1 November 2022, Pages 3741–3756, https://doi.org/10.1093/hmg/ddac137
Published: 18 June 2022
Journal Article
Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastoma
Shaobo Li and others
Neuro-Oncology Advances, Volume 4, Issue 1, January-December 2022, vdac045, https://doi.org/10.1093/noajnl/vdac045
Published: 13 April 2022
Journal Article
Trends in Acute Lymphoblastic Leukemia Incidence in the United States by Race/Ethnicity From 2000 to 2016
Qianxi Feng and others
American Journal of Epidemiology, Volume 190, Issue 4, April 2021, Pages 519–527, https://doi.org/10.1093/aje/kwaa215
Published: 09 October 2020
Journal Article
Pediatric glioma and medulloblastoma risk and population demographics: a Poisson regression analysis
Ivo S Muskens and others
Neuro-Oncology Advances, Volume 2, Issue 1, January-December 2020, vdaa089, https://doi.org/10.1093/noajnl/vdaa089
Published: 22 July 2020
Journal Article
European genetic ancestry associated with risk of childhood ependymoma
Chenan Zhang and others
Neuro-Oncology, Volume 22, Issue 11, November 2020, Pages 1637–1646, https://doi.org/10.1093/neuonc/noaa130
Published: 02 June 2020
Journal Article
History of Early Childhood Infections and Acute Lymphoblastic Leukemia Risk Among Children in a US Integrated Health-Care System
Libby M Morimoto and others
American Journal of Epidemiology, Volume 189, Issue 10, October 2020, Pages 1076–1085, https://doi.org/10.1093/aje/kwaa062
Published: 23 April 2020
Journal Article
Germline cancer predisposition variants and pediatric glioma: a population-based study in California
Ivo S Muskens and others
Neuro-Oncology, Volume 22, Issue 6, June 2020, Pages 864–874, https://doi.org/10.1093/neuonc/noaa014
Published: 23 January 2020
Journal Article
Germline genetic landscape of pediatric central nervous system tumors
Ivo S Muskens and others
Neuro-Oncology, Volume 21, Issue 11, November 2019, Pages 1376–1388, https://doi.org/10.1093/neuonc/noz108
Published: 19 June 2019
Journal Article
Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers
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Kyle M. Walsh and others
Carcinogenesis, Volume 37, Issue 6, June 2016, Pages 576–582, https://doi.org/10.1093/carcin/bgw037
Published: 01 April 2016
Journal Article
Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion
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Kristen Martins-Taylor and others
Human Molecular Genetics, Volume 23, Issue 9, 1 May 2014, Pages 2364–2373, https://doi.org/10.1093/hmg/ddt628
Published: 20 December 2013
Journal Article
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity
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Julia S. El-Sayed Moustafa and others
Human Molecular Genetics, Volume 21, Issue 16, 15 August 2012, Pages 3727–3738, https://doi.org/10.1093/hmg/dds187
Published: 16 May 2012
Journal Article
Accurate Single-Nucleotide Polymorphism Allele Assignment in Trisomic or Duplicated Regions by Using a Single Base–Extension Assay with MALDI-TOF Mass Spectrometry
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Anne L Trewick and others
Clinical Chemistry, Volume 57, Issue 8, 1 August 2011, Pages 1188–1195, https://doi.org/10.1373/clinchem.2010.159558
Published: 01 August 2011
Includes: Multimedia
Journal Article
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
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Adam J. de Smith and others
Human Molecular Genetics, Volume 18, Issue 17, 1 September 2009, Pages 3257–3265, https://doi.org/10.1093/hmg/ddp263
Published: 04 June 2009
Journal Article
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases
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Adam J. de Smith and others
Human Molecular Genetics, Volume 16, Issue 23, 1 December 2007, Pages 2783–2794, https://doi.org/10.1093/hmg/ddm208
Published: 31 July 2007
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