Publications:

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Circadian stabilization loop: the regulatory hub and therapeutic target promoting circadian resilience and physiological health.

F1000Research

Kim, Eunju E; Yoo, Seung-Hee SH; Chen, Zheng Z

Publication Date: 2022

Variant appearance in text: rs7164773

PubMed Link: 36415204

Variant Present in the following documents:

• Main text
• f1000research-11-138767.pdf

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A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG.

Frontiers In Genetics

Haaland, Øystein A ØA; Lie, Rolv T RT; Romanowska, Julia J; Gjerdevik, Miriam M; Gjessing, Håkon K HK; Jugessur, Astanand A

Publication Date: 2018

Variant appearance in text: rs7164773

PubMed Link: 29535761

Variant Present in the following documents:

• Main text

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Circadian pathway genetic variation and cancer risk: evidence from genome-wide association studies.

Bmc Medicine

Mocellin, Simone S; Tropea, Saveria S; Benna, Clara C; Rossi, Carlo Riccardo CR

Publication Date: 2018-02-19

Variant appearance in text: rs7164773

PubMed Link: 29455641

Variant Present in the following documents:

• Main text
• 12916_2018_Article_1010.pdf

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Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival.

International Journal Of Cancer

Li, Bo B; Wang, Yanru Y; Xu, Yinghui Y; Liu, Hongliang H; Bloomer, Wendy W; Zhu, Dakai D; Amos, Christopher I CI; Fang, Shenying S; Lee, Jeffrey E JE; Li, Xin X; Han, Jiali J; Wei, Qingyi Q

Publication Date: 2018-06-01

Variant appearance in text: rs7164773

PubMed Link: 29313974

Variant Present in the following documents:

• Main text

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Genetic Epidemiology of Type 2 Diabetes in Mexican Mestizos.

Biomed Research International

García-Chapa, Eiralí Guadalupe EG; Leal-Ugarte, Evelia E; Peralta-Leal, Valeria V; Durán-González, Jorge J; Meza-Espinoza, Juan Pablo JP

Publication Date: 2017

Variant appearance in text: rs7164773

PubMed Link: 28607931

Variant Present in the following documents:

• Main text
• BMRI2017-3937893.pdf

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Immune-related gene polymorphisms in pulmonary diseases.

Toxicology

Singh, Dhirendra P DP; Bagam, Prathyusha P; Sahoo, Malaya K MK; Batra, Sanjay S

Publication Date: 2017-05-15

Variant appearance in text: rs7164773

PubMed Link: 28366820

Variant Present in the following documents:

• Main text

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Genetic variation of clock genes and cancer risk: a field synopsis and meta-analysis.

Oncotarget

Benna, Clara C; Helfrich-Förster, Charlotte C; Rajendran, Senthilkumar S; Monticelli, Halenya H; Pilati, Pierluigi P; Nitti, Donato D; Mocellin, Simone S

Publication Date: 2017-04-04

Variant appearance in text: rs7164773

PubMed Link: 28177907

Variant Present in the following documents:

• Main text
• oncotarget-08-23978.pdf

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Retinoic Acid-Related Orphan Receptors (RORs): Regulatory Functions in Immunity, Development, Circadian Rhythm, and Metabolism.

Nuclear Receptor Research

Cook, Donald N DN; Kang, Hong Soon HS; Jetten, Anton M AM

Publication Date: 2015

Variant appearance in text: rs7164773

PubMed Link: 26878025

Variant Present in the following documents:

• Main text
• nihms746408.pdf

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Rule-based models of the interplay between genetic and environmental factors in childhood allergy.

Plos One

Bornelöv, Susanne S; Sääf, Annika A; Melén, Erik E; Bergström, Anna A; Torabi Moghadam, Behrooz B; Pulkkinen, Ville V; Acevedo, Nathalie N; Orsmark Pietras, Christina C; Ege, Markus M; Braun-Fahrländer, Charlotte C; Riedler, Josef J; Doekes, Gert G; Kabesch, Michael M; van Hage, Marianne M; Kere, Juha J; Scheynius, Annika A; Söderhäll, Cilla C; Pershagen, Göran G; Komorowski, Jan J

Publication Date: 2013

Variant appearance in text: rs7164773

PubMed Link: 24260339

Variant Present in the following documents:

• pone.0080080.s003.xls, sheet 1

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Interaction between retinoid acid receptor-related orphan receptor alpha (RORA) and neuropeptide S receptor 1 (NPSR1) in asthma.

Plos One

Acevedo, Nathalie N; Sääf, Annika A; Söderhäll, Cilla C; Melén, Erik E; Mandelin, Jami J; Pietras, Christina Orsmark CO; Ezer, Sini S; Karisola, Piia P; Vendelin, Johanna J; Gennäs, Gustav Boije af GB; Yli-Kauhaluoma, Jari J; Alenius, Harri H; von Mutius, Erika E; Doekes, Gert G; Braun-Fahrländer, Charlotte C; Riedler, Josef J; van Hage, Marianne M; D'Amato, Mauro M; Scheynius, Annika A; Pershagen, Göran G; Kere, Juha J; Pulkkinen, Ville V

Publication Date: 2013

Variant appearance in text: rs7164773

PubMed Link: 23565190

Variant Present in the following documents:

• Main text

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Retinoic acid-related orphan receptors α and γ: key regulators of lipid/glucose metabolism, inflammation, and insulin sensitivity.

Frontiers In Endocrinology

Jetten, Anton M AM; Kang, Hong Soon HS; Takeda, Yukimasa Y

Publication Date: 2013

Variant appearance in text: rs7164773

PubMed Link: 23355833

Variant Present in the following documents:

• Main text

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Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.

Diabetes

Gamboa-Meléndez, Marco Alberto MA; Huerta-Chagoya, Alicia A; Moreno-Macías, Hortensia H; Vázquez-Cárdenas, Paola P; Ordóñez-Sánchez, María Luisa ML; Rodríguez-Guillén, Rosario R; Riba, Laura L; Rodríguez-Torres, Maribel M; Guerra-García, María Teresa MT; Guillén-Pineda, Luz Elizabeth LE; Choudhry, Shweta S; Del Bosque-Plata, Laura L; Canizales-Quinteros, Samuel S; Pérez-Ortiz, Gustavo G; Escobedo-Aguirre, Fernando F; Parra, Adalberto A; Lerman-Garber, Israel I; Aguilar-Salinas, Carlos Alberto CA; Tusié-Luna, María Teresa MT

Publication Date: 2012-12

Variant appearance in text: rs7164773

PubMed Link: 22923468

Variant Present in the following documents:

• Main text
• 3314.pdf

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Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.

American Journal Of Human Genetics

El-Sayed, Walid W; Parry, David A DA; Shore, Roger C RC; Ahmed, Mushtaq M; Jafri, Hussain H; Rashid, Yasmin Y; Al-Bahlani, Suhaila S; Al Harasi, Sharifa S; Kirkham, Jennifer J; Inglehearn, Chris F CF; Mighell, Alan J AJ

Publication Date: 2009-11

Variant appearance in text: rs7164773

PubMed Link: 19853237

Variant Present in the following documents:

• mmc1.pdf

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