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Frontiers in Oncology|July 5, 2016
Polymorphisms of Insulin-Like Growth Factor 1 Pathway Genes and Breast Cancer RiskJoy Shi, Kristan J Aronson, Anne Grundy, et al.
Molecular Vision|December 6, 2012
Absence of NR2E1 mutations in patients with aniridiaXimena Corso-Díaz, Adrienne E Borrie, Russell Bonaguro, et al.
Plos One|October 8, 2013
Non-Hodgkin lymphoma risk and variants in genes controlling lymphocyte developmentJohanna M Schuetz, Denise Daley, Stephen Leach, et al.
Scientific Reports|December 30, 2022
Profiling placental DNA methylation associated with maternal SSRI treatment during pregnancyAmy M Inkster, Chaini Konwar, Maria S Peñaherrera, et al.
Leukemia|December 23, 2011
BCL2 mutations in diffuse large B-cell lymphomaJ M Schuetz, N A Johnson, R D Morin, et al.
Plos One|September 27, 2013
Sex- and subtype-specific analysis of H2AFX polymorphisms in non-Hodgkin lymphomaKarla L Bretherick, Johanna M Schuetz, Lindsay M Morton, et al.
Research Square|July 18, 2023
The application of epiphenotyping approaches to DNA methylation array studies of the human placentaAlmas Khan, Amy M Inkster, Maria S Peñaherrera, et al.
Epigenetics & Chromatin|October 4, 2023
The application of epiphenotyping approaches to DNA methylation array studies of the human placentaA Khan, A M Inkster, M S Peñaherrera, et al.
Insights Into Imaging|August 14, 2024
The effectiveness of coronary computed tomography angiography and functional testing for the diagnosis of obstructive coronary artery disease: results from the individual patient data Collaborative Meta-Analysis of Cardiac CT (COME-CCT)Peter Schlattmann, Viktoria Wieske, Keno K Bressem, et al.
Orphanet Journal of Rare Diseases|May 23, 2026
Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephalyChristiane R Proepper, Lisa-Maria Schwarz, Sofia M Schuetz, et al.
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