Historical linkages: epidemic threat, economic risk, and xenophobia
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Reckoning with histories of medical racism and violence in the USA
Nuriddin, Ayah, Mooney, Graham, White, Alexandre I R
Published in The Lancet (British edition) (03.10.2020)
Published in The Lancet (British edition) (03.10.2020)
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Racism, xenophobia, discrimination, and the determination of health
Devakumar, Delan, Selvarajah, Sujitha, Abubakar, Ibrahim, Kim, Seung-Sup, McKee, Martin, Sabharwal, Nidhi S, Saini, Angela, Shannon, Geordan, White, Alexandre I R, Achiume, E Tendayi
Published in The Lancet (British edition) (10.12.2022)
Published in The Lancet (British edition) (10.12.2022)
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Missense variant in SRCAP with distinct DNA methylation signature associated with non-FLHS SRCAP-related neurodevelopmental disorder
White-Brown, Alexandre, Choufani, Sanaa, Weksberg, Rosanna, Dyment, David
Published in American journal of medical genetics. Part A (01.10.2023)
Published in American journal of medical genetics. Part A (01.10.2023)
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The public’s role in COVID-19 vaccination: Human-centered recommendations to enhance pandemic vaccine awareness, access, and acceptance in the United States
Schoch-Spana, Monica, Brunson, Emily K., Long, Rex, Ruth, Alexandra, Ravi, Sanjana J., Trotochaud, Marc, Borio, Luciana, Brewer, Janesse, Buccina, Joseph, Connell, Nancy, Hall, Laura Lee, Kass, Nancy, Kirkland, Anna, Koonin, Lisa, Larson, Heidi, Lu, Brooke Fisher, Omer, Saad B., Orenstein, Walter A., Poland, Gregory A., Privor-Dumm, Lois, Quinn, Sandra Crouse, Salmon, Daniel, White, Alexandre
Published in Vaccine (24.09.2021)
Published in Vaccine (24.09.2021)
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Further characterization of CEP85L ‐associated lissencephaly type 10: Report of a three‐generation family and review of the literature
Leduc‐Pessah, Heather, White‐Brown, Alexandre, Miller, Elka, McMillan, Hugh J., Boycott, Kym M.
Published in American journal of medical genetics. Part A (01.12.2023)
Published in American journal of medical genetics. Part A (01.12.2023)
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A disease‐causing variant in HNRNPH2 inherited from an unaffected mother with skewed X‐inactivation
White‐Brown, Alexandre M., Lemire, Gabrielle, Ito, Yoko A., Thornburg, Olivia, Bain, Jennifer M., Dyment, David A.
Published in American journal of medical genetics. Part A (01.02.2022)
Published in American journal of medical genetics. Part A (01.02.2022)
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PRKAG2 ‐Related Lethal Congenital Glycogen Storage Disease of the Heart as Rare Cause of Fetal Hydrops With Bradycardia and Cardiomyopathy: Clinical Report and Literature Review
White‐Brown, Alexandre M., Richard, Marilyn, Morency, Anne‐Maude, Maedler‐Kron, Chelsea, De Bie, Isabelle
Published in American journal of medical genetics. Part A (30.08.2024)
Published in American journal of medical genetics. Part A (30.08.2024)
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Categorisation and Minoritisation
Selvarajah, Sujitha, Deivanayagam, Thilagawathi Abi, Lasco, Gideon, Scafe, Suzanne, White, Alexandre, Zembe-Mkabile, Wanga, Devakumar, Delan
Published in BMJ global health (01.12.2020)
Published in BMJ global health (01.12.2020)
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Residential racial segregation and social distancing in the United States during COVID-19
White, Alexandre, Hao, Lingxin, Yu, Xiao, Thorpe, Roland J.
Published in EClinicalMedicine (01.05.2021)
Published in EClinicalMedicine (01.05.2021)
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Genetically unresolved case of Rauch-Steindl syndrome diagnosed by its wolf-hirschhorn associated DNA methylation episignature
McConkey, Haley, White-Brown, Alexandre, Kerkhof, Jennifer, Dyment, David, Sadikovic, Bekim
Published in Frontiers in cell and developmental biology (15.12.2022)
Published in Frontiers in cell and developmental biology (15.12.2022)
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The Benefit of Multigene Panel Testing for the Diagnosis and Management of the Genetic Epilepsies
Leduc-Pessah, Heather, White-Brown, Alexandre, Hartley, Taila, Pohl, Daniela, Dyment, David A
Published in Genes (13.05.2022)
Published in Genes (13.05.2022)
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