Human Genome Epidemiology Literature Finder
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PD-L1 Expression is not a Predictive Factor for Recurrence in Resected Non-small Cell Lung Cancer. Lung 2022 12 201 (1): 95-101. Motono Nozomu, Mizoguchi Takaki, Ishikawa Masahito, Iwai Shun, Iijima Yoshihito, Uramoto Hideta |
Significant association between HLA-B*35:01 and onset of drug-induced liver injury caused by Kampo medicines in Japanese patients. Hepatology research : the official journal of the Japan Society of Hepatology 2022 12 . Nakamura Ryosuke, Arakawa Noriaki, Tanaka Yoichi, Uchiyama Nahoko, Sekine Akihiro, Mashimo Yoichi, Tsuji Keiji, Kagawa Tatehiro, Sato Ken, Watanabe Masaaki, Aiso Mitsuhiko, Hiasa Yoichi, Takei Yoshiyuki, Ohira Hiromasa, Ayada Minoru, Tsukagoshi Eri, Maekawa Keiko, Tohkin Masahiro, Saito Yoshiro, Takikawa Haji |
Impact of Serotonin Pathway Gene Polymorphisms and Serotonin Levels in Suicidal Behavior. Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2023 9 . Sneha Sivaramakrishnan, Vettriselvi Venkatesan, Sampath Kumar Paranthaman, R Sathianathan, Swetha Raghavan, Priyadarshee Pradh |
Irinotecan-Induced Toxicity: A Pharmacogenetic Study Beyond UGT1A1. Clinical pharmacokinetics 2023 9 . Mirjam de With, Leni van Doorn, Esmay Kloet, Anne van Veggel, Maja Matic, Micha J de Neijs, Esther Oomen-de Hoop, Esther van Meerten, Ron H N van Schaik, Ron H J Mathijssen, Sander Bi |
Association between Chinese herbal medicine (CHM) treatment and depression among cancer patients in China: An outpatient-based cross-sectional study. Medicine 2023 9 102 (34): e34695. Huiyue Lin, Xueting Zhang, Yi Zhang, Wenjing Cui, Fang Jia, Juyong Wa |
Vitamin D and vitamin D receptor polymorphism in Asian adolescents with primary dysmenorrhea. BMC women's health 2023 8 23 (1): 414. Ainur Donayeva, Ainur Amanzholkyzy, Roza Nurgaliyeva, Gulnara Gubasheva, Samat Saparbayev, Dinmukhamed Ayaganov, Aiman Kaldybayeva, Ibrahim A Abdelazim, Mohamed M Fargha |
VDR, SOD-2, and CYP24A1 Gene Expression in Different Genotypes of BsmI SNP of the Vitamin D Receptor Gene in Individuals with Hypovitaminosis. Nutrients 2023 8 15 (16): . Vanessa Rosa Retamoso, Fernanda Barbisan, Graziele Meira Moro, Patricia Maurer, Débora Vasquez Rubio, Lauren Flores Viera Dos Santos, Lyana Berro Feijóo, Matias Nunes Frizzo, Ivana Beatrice Mânica da Cruz, Vanusa Manfredini, Ana Letícia Vargas Barcelos, Jacqueline da Costa Escobar Picco |
Association of CYP2C9*2 Allele with Sulphonylurea-Induced Hypoglycaemia in Type 2 Diabetes Mellitus Patients: A Pharmacogenetic Study in Pakistani Pashtun Population. Biomedicines 2023 8 11 (8): . Asif Jan, Muhammad Saeed, Ramzi A Mothana, Tahir Muhammad, Naveed Rahman, Abdullah R Alanzi, Rani Akb |
Exome sequencing in a Romanian Bardet-Biedl syndrome cohort revealed an overabundance of causal BBS12 variants. American journal of medical genetics. Part A 2023 6 . Sheraz Khan, Ina Ofelia Foc?a, Magdalena Budi?teanu, Cristina Stoica, Florina Nedelea, Lauren?iu Bohîl?ea, Lavinia Caba, L?cr?mioara Butnariu, Monica Pânzaru, Cristina Rusu, Claudia Jurc?, Adela Chirita-Emandi, Claudia B?nescu, Wasim Abbas, Azita Sadeghpour, Shahid Mahmood Baig, Mihaela B?lgr?dean, Erica E Dav |
Effect of the Angiotensin-Converting Enzyme (ACE) (I/D) Polymorphism in COVID-19 Patients and Their Healthy Contacts. Cureus 2023 6 15 (5): e38610. Prishni Gupta, Eli Mohapatra, Suprava Patel, Lisie L Patnayak, Rachita Nanda, Seema Shah, Jessy Abraham, Ajoy Behera, Atul Jind |
Prevalence of Hearing Loss in Type 2 Diabetes Mellitus and Its Association with Severity of Diabetic Neuropathy and Glycemic Control. The Journal of the Association of Physicians of India 2023 6 71 (6): 11-12. Abin M Abraham, Jubbin Jagan Jacob, Ashish Varghe |
Study of genetic variants and their clinical significance in Mexican pediatric patients with epilepsy. Gene 2023 6 877 147565. Iris A Feria-Romero, Aracely Reyes-Cuayahuitl, Justina Sosa-Maldonado, Alexia V Montes-Aparicio, Darío Rayo-Mares, Daniel Pérez-Pérez, Israel Grijalva-Otero, Sandra Orozco-Suar |
Association between HMGB1 genetic variants and ischemic stroke susceptibility, onset age, and recurrence risk among Chinese Han individuals. American journal of translational research 2023 6 15 (5): 3326-3341. Luying Qiu, Long Li, Zhiyi He, Fang Liu, Shumin Deng, Yanzhe Wa |
Chronic inflammatory intestinal disorders in hidradenitis suppurativa. Dermatology (Basel, Switzerland) 2023 4 . Réka Palatka, Janka Eszter Anna, Soltész Lilla, Szabó Imre L?rinc, Kapitány Anikó, Dajnoki Zsolt, Emri Gabriella, Nagy Gábor, Palatka Károly, Zouboulis Christos C, Szegedi Andrea, Gáspár Kriszti |
Risk Factors of Incident Kidney Stones in Indian Adults: A Hospital-Based Cross-Sectional Study. Cureus 2023 4 15 (2): e35558. Singh Smriti, Gupta Sanjay, Mishra Tushar, Banerjee Basu Dev, Sharma Tus |
Risk factor of elevated matrix metalloproteinase-3 gene expression in synovial fluid in knee osteoarthritis women. PloS one 2023 3 18 (3): e0283831. Sulastri Delmi, Arnadi Arnadi, Afriwardi Afriwardi, Desmawati Desmawati, Amir Arni, Irawati Nuzulia, Yanis Amel, Yusrawati Yusrawa |
Protein Intake Is Associated with Blood Pressure and Cholesterol Levels in Italian Older Adults: A Cross-Sectional Study. Metabolites 2023 3 13 (3): . Coelho-Júnior Hélio José, Calvani Riccardo, Picca Anna, Tosato Matteo, Savera Giulia, Landi Francesco, Marzetti Emanue |
Germline Mutations Landscape in a Cohort of the State of Minas Gerais, Brazil, in Patients Who Underwent Genetic Counseling for Gynecological and Breast Cancer. Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia 2023 3 45 (2): 74-81. Carvalho Camila Martins de, Braga Letícia da Conceição, Silva Luciana Maria, Chami Anisse Marques, Silva Filho Agnaldo Lopes |
Contribution of NOS3AS Variants to Susceptibility to Essential Hypertension: A Study in Kermanshah Province, Western Iran. Biochemical genetics 2023 3 . Karami Bahareh, Azimi Azam, Rahimi Zohreh, Mahmoudi Sousan, Jalilian Nazan |
[Ala54Thr polymorphism of the fatty acid transporter gene (FABP2) in patients with type 2 diabetes mellitus in Yakutia]. Terapevticheskii arkhiv 2023 12 95 (10): 845-849. L A Sydykova, N I Pavlova, A A Bochurov, V A Alekseev, A V Krylov, K A Kurtanov, M V Shestako |
Association of ITPA 94C>A genetic polymorphisms with azathioprine induced adverse effects in the South Indian population. Drug metabolism and personalized therapy 2023 12 . Reka Deva, Priyadharsini Rajendran, Sivaranjani Ramasamy, Senthamizh Selvan, Kesavan Ramasa |
Genetic Association of the C-C Motif Chemokine Ligand 2 (CCL2) rs1024611 Polymorphism With Periodontitis. Cureus 2023 11 15 (10): e46438. Hooriyah Laiq Ahmed Khan, Karthikeyan Murthykumar, Dhanraj Ganapat |
DRD4 VNTR 4/4 homozygosity as a genetic biomarker for treatment selection in patients with schizophrenia. Asian journal of psychiatry 2023 11 91 103831. Hao-Ming Yang, Hsuan Lung, Ming-Chang Yang, For-Wey Lu |
ASSOCIATION BETWEEN GLN27GLU POLYMORPHISM IN THE ?2 ADRENERGIC RECEPTOR GENE AND OBESITY RISK IN PATIENTS WITH EARLY-ONSET AND LATE-ONSET BRONCHIAL ASTHMA. Georgian medical news 2023 10 (340-341): 254-258. V Kachkovs |
Genome-Wide Association Study Identifies Novel Candidate Variants Associated with Postoperative Nausea and Vomiting. Cancers 2023 10 15 (19): . Daisuke Nishizawa, Ryozo Morino, Rie Inoue, Seii Ohka, Shinya Kasai, Junko Hasegawa, Yuko Ebata, Kyoko Nakayama, Hiroyuki Sumikura, Masakazu Hayashida, Miyuki Yokota, Kazutaka Ike |
Association of the BB genotype of the ABO gene with the risk of acute myocardial infarction in hospital-based study. Pakistan journal of medical sciences 2023 1 39 (1): 133-138. Yousuf Farzana Abubakar, Azam Iqbal, Tareen Asal Khan, Kazmi Khawar A, Muhammad Jibran Sualeh, Iqbal Mohammad Perwa |
Capecitabine-induced hand-foot syndrome: A pharmacogenetic study beyond DPYD. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2023 1 159 114232. de With Mirjam, van Doorn Leni, Maasland Demi C, Mulder Tessa A M, Oomen-de Hoop Esther, Mostert Bianca, Homs Marjolein Y V, El Bouazzaoui Samira, Mathijssen Ron H J, van Schaik Ron H N, Bins Sand |
Prevalence of CYP2C19*2 and CYP2C19*3 Allelic Variants and Clopidogrel Use in Patients with Cardiovascular Disease in Trinidad & Tobago. Cardiology and therapy 2024 1 . Daniele Jones, Shana Persad-Ramdeensingh, Sheherazade Crystal Abrahim, Naveen Seecheran, Rajini Rani Haraksin |
Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study. Journal of thoracic disease 2024 1 15 (12): 7013-7023. Yalei Zhang, Yan Hao, Hui Pan, Hongbo Zheng, Jiaqi Zh |
The Effect of FSHR (G2039A) Polymorphism on Müllerian Duct Development and Hormonal Profile of Women with Primary Amenorrhea. Journal of reproduction & infertility 2024 1 24 (4): 240-247. Priyanka Sanghavi, Divya Chand |
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- Page last updated:Apr 29, 2024
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