Results 221 to 230 of about 372,458 (325)

Genetic Predisposition Toward Multicellularity in Chlamydomonas reinhardtii. [PDF]

Genome Biol Evol
Chen ICK, Khatri S, Herron MD, Rosenzweig F.   +3 more
europepmc   +1 more source

Genetic Predisposition to Higher Blood Pressure Increases Coronary Artery Disease Risk [PDF]

, 2013
Wolfgang Lieb, Henning Jansen, Christina Loley, Michael J. Pencina, Christopher P. Nelson, Christopher Newton‐Cheh, Sekar Kathiresan, Muredach P. Reilly, Themistocles L. Assimes, Eric Boerwinkle, Alistair S. Hall, Christian Hengstenberg, Reijo Laaksonen, Ruth McPherson, Unnur Þorsteinsdóttir, Andreas Ziegler, Annette Peters, John R. Thompson, Inke R. König, Jeanette Erdmann, Nilesh J. Samani, Ramachandran S. Vasan, Heribert Schunkert   +22 more
openalex   +1 more source

Genetic predisposition [PDF]

, 2019
openaire   +1 more source

Promoting radical healing to facilitate community capacity building among formerly incarcerated Black and Latino men with substance use disorders

American Journal of Community Psychology, EarlyView.
Abstract This study reports on a qualitative thematic analysis of secondary data from group session recordings collected as part of the Community Wise Optimization Trial. Community Wise is a multilevel behavioral intervention designed to increase critical consciousness and reduce substance use among formerly incarcerated men living in predominantly ...
Richmond E. Hayes, Heather A. Jones, Ellen Benoit, Dora N. Watkins, Liliane C. Windsor   +4 more
wiley   +1 more source

Genetic predisposition and the impact of missense genetic variants on the structural and functional protein dynamics in idiopathic pulmonary fibrosis. [PDF]

Lung India
Barney AM, Isaac B, Christopher DJ, Thangakunam B, Balaji J, Mohan VR, Christudass CS, Danda D, Danda S.   +8 more
europepmc   +1 more source

A genetic risk tool for obesity predisposition assessment and personalized nutrition implementation based on macronutrient intake [PDF]

, 2014
Leticia Goñi, Marta Cuervo, Fermı́n I. Milagro, J. Alfredo Martínéz   +3 more
openalex   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Molecular Profiling of Genes Associated With Methylphenidate Pathway Therapy and Discovery of New Variants in Amazonian Amerindian Populations

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT In Attention Deficit Hyperactivity Disorder (ADHD), methylphenidate is one of the most widely used drugs, in which patient response significantly impacts prognosis. This study aimed to characterize the molecular profile of 10 genes associated with methylphenidate therapy.
Aline Pasquini Santos, Tatiane Carinta de Souza, Kaio Evandro Cardoso Aguiar, Ana Caroline Alves da Costa, Natasha Monte, Juliana Carla Gomes Rodrigues, Giovanna Gilioli da Costa Nunes, Rita de Cássia Calderaro Coelho, Ândrea Ribeiro‐dos‐Santos, André Maurício Ribeiro dos Santos, Sandro José de Souza, Sidney Emanuel Batista dos Santos, Rommel Mario Rodriguez Burbano, Marianne Rodrigues Fernandes, Ney Pereira Carneiro dos Santos   +14 more
wiley   +1 more source

Frailty, genetic predisposition, and incident chronic kidney disease. [PDF]

Sci Rep
Zou S, Sun Y, Zhou Y, Yu B, Li J, Yu Y, Chen J, Li Y, Wang N, Wang L.   +9 more
europepmc   +1 more source

Rüdin's Unpublished Family Study From the Early 1920s: “On the Inheritance of Manic‐Depressive Insanity”

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Ernst Rüdin, an important and controversial figure in the history of psychiatric genetics, published only one major empirical study on siblings of dementia praecox (DP) probands in 1916. He conducted a parallel study of siblings of probands with manic‐depressive insanity (MDI), but the resulting monograph, written in the early 1920s, was left ...
Kenneth S. Kendler, Astrid Klee
wiley   +1 more source