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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 12 (of 12 Records)

Query Trace: Obesity and FH[original query]
Impact of genetic defects on atherosclerosis in patients suspected of familial hypercholesterolaemia.
European journal of clinical investigation 2001 Nov 31 (11): 958-65.
Descamps O S, Gilbeau J P, Leysen X, Van Leuven F, Heller F
Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia.
The Journal of clinical endocrinology and metabolism 2009 Nov 94 (11): 4391-7.
Solanas-Barca María, Mateo-Gallego Rocío, Calmarza Pilar, Jarauta Estíbaliz, Bea Ana M, Cenarro Ana, Civeira Fernan
Association of the UCP-1 single nucleotide polymorphism A-3826G with the dampness-phlegm pattern among Korean stroke patients.
BMC complementary and alternative medicine 2012 Oct 12 (1): 1.
Lim JH, Ko MM, Moon TW, Lee MS, Cha MH
Multiple hits for the association of uterine fibroids on human chromosome 1q43.
PloS one 2013 8 (3): e58399.
Aissani Brahim, Wiener Howard, Zhang K
ADRB3 gene promoter DNA methylation in blood and visceral adipose tissue is associated with metabolic disturbances in men.
Epigenomics 2014 Feb 6 (1): 33-43.
Guay Simon-Pierre, Brisson Diane, Lamarche Benoit, Biron Simon, Lescelleur Odette, Biertho Laurent, Marceau Simon, Vohl Marie-Claude, Gaudet Daniel, Bouchard Lui
Health related quality of life in individuals at high risk for familial hypercholesterolemia undergoing genetic cascade screening in Brazil.
Atherosclerosis 2018 10 277 464-469.
Souto Ana Cristina, Miname Marcio H, Fukushima Julia, Jannes Cinthia E, Krieger Jose E, Hagger Martin, Pereira Alexandre C, Santos Raul
Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction.
Lipids in health and disease 2019 Apr 18 (1): 95.
Lee Chongyou, Cui Yuxia, Song Junxian, Li Sufang, Zhang Feng, Wu Manyan, Li Long, Hu Dan, Chen Ho
Outcomes of Patients with Central Precocious Puberty Due to Loss-of-Function Mutations in the MKRN3 Gene after Treatment with Gonadotropin-Releasing Hormone Analog.
Neuroendocrinology 2019 11 110 (7-8): 705-713.
Ramos Carolina de Oliveira, Macedo Delanie B, Canton Ana Pinheiro M, Cunha-Silva Marina, Antonini Sonir R R, Stecchini Monica Freire, Seraphim Carlos Eduardo, Rodrigues Tania, Mendonca Berenice Bilharinho, Latronico Ana Claudia, Brito Vinicius Nahi
Reducing cardiovascular risk in patients with familial hypercholesterolemia: Risk prediction and lipid management.
Progress in cardiovascular diseases 2019 11 62 (5): 414-422.
Miname Marcio H, Santos Raul
A variant in the fibronectin (FN1) gene, rs1250229-T, is associated with decreased risk of coronary artery disease in familial hypercholesterolaemia.
Journal of clinical lipidology 2022 May .
Page Michael M, Ellis Katrina L, Chan Dick C, Pang Jing, Hooper Amanda J, Bell Damon A, Burnett John R, Moses Eric K, Watts Gerald
Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family history.
BMC medical genomics 2023 7 16 (1): 164.
Emadeldin Hassanin, Carlo Maj, Hannah Klinkhammer, Peter Krawitz, Patrick May, Dheeraj Reddy Bobbi
Impact of Healthy Lifestyle in Patients With Familial Hypercholesterolemia.
JACC. Asia 2023 3 3 (1): 152-160.
Tada Hayato, Kojima Nobuko, Yamagami Kan, Nomura Akihiro, Nohara Atsushi, Usui Soichiro, Sakata Kenji, Hayashi Kenshi, Fujino Noboru, Takamura Masayuki, Kawashiri Masa-A
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