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Kidney International|December 21, 2007
A proposed nomenclature and diagnostic criteria for protein-energy wasting in acute and chronic kidney diseaseD Fouque, K Kalantar-Zadeh, J Kopple, et al.
Cell Reports|October 24, 2024
Comparing neoantigen cancer vaccines and immune checkpoint therapy unveils an effective vaccine and anti-TREM2 macrophage-targeting dual therapySunita Keshari, Alexander S Shavkunov, Qi Miao, et al.
Human Mutation|July 16, 2009
The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesisErich Roessler, Kenia B El-Jaick, Christèle Dubourg, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|November 12, 2015
Home management of acute medical complications in cancer patients: a prospective pilot studyC Font, F Fernández-Avilés, C Calderon, et al.
JCO Global Oncology|July 22, 2022
Germline Pathogenic Variant Prevalence Among Latin American and US Hispanic Individuals Undergoing Testing for Hereditary Breast and Ovarian Cancer: A Cross-Sectional StudyCarlos Andrés Ossa Gomez, Maria Isabel Achatz, Mabel Hurtado, et al.
Molecular Genetics and Metabolism|July 20, 2011
Personalized genomic medicine: lessons from the exomeBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
STAT3 protects HSCs from intrinsic interferon signaling and loss of long-term blood-forming activityBhakti Patel, Yifan Zhou, Rachel L Babcock, et al.
Attention Deficit and Hyperactivity Disorders|July 23, 2011
Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolateDavid A Pineda, Francisco Lopera, Isabel C Puerta, et al.
JACC. Advances|July 4, 2025
Cardiologists' Perceptions of Cardiogenetic Testing and ManagementW H Wilson Tang, Quan M Bui, Allison L Cirino, et al.
Human Mutation|September 9, 2020
Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretationElizabeth M McCormick, Marie T Lott, Matthew C Dulik, et al.
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