Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 110 Records) |
Query Trace: MBP[original query] |
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A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect. Molecular genetics & genomic medicine 2019 11 8 (2): e1070. Dawson Lesa M, Smith Kerri N, Werdyani Salem, Ndikumana Robyn, Penney Cindy, Wiede Louisa L, Smith Kendra L, Pater Justin A, MacMillan Andrée, Green Jane, Drover Sheila, Young Terry-Lynn, O'Rielly Darren |
Clinical implications of next-generation sequencing-based panel tests for malignant ovarian tumors. Cancer medicine 2020 Aug . Saotome Keiko, Chiyoda Tatsuyuki, Aimono Eriko, Nakamura Kohei, Tanishima Shigeki, Nohara Sachio, Okada Chihiro, Hayashi Hideyuki, Kuroda Yuka, Nomura Hiroyuki, Susumu Nobuyuki, Iwata Takashi, Yamagami Wataru, Kataoka Fumio, Nishihara Hiroshi, Aoki Daisu |
Influence of Genetic Admixture Components on CYP3A5*3 Allele-Associated Hypertension in Amerindian Populations From Northwest Mexico. Frontiers in pharmacology 2020 6 11 638. Galaviz-Hernández Carlos, Lazalde-Ramos Blanca P, Lares-Assef Ismael, Macías-Salas Alejo, Ortega-Chavez Margarita A, Rangel-Villalobos Héctor, Sosa-Macías Mart |
A Polymorphism Within the MBP Gene Is Associated With a Higher Relapse Number in Male Patients of Multiple Sclerosis. Frontiers in immunology 2020 11 771. Espino-Paisán Laura, Agudo-Jiménez Teresa, Rosales-Martínez Isabel, López-Cotarelo Pilar, García-Martínez María Ángel, Domínguez-Mozo María Inmaculada, Pérez-Pérez Silvia, Dieli-Crimi Romina, Comabella Manuel, Urcelay Elena, Álvarez-Lafuente Rober |
Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome. European journal of pediatrics 2020 3 179 (9): 1481-1486. Korsgaard Trine, Joshi Shivani, Andersen Rene F, Moeller Kristina, Seeman Tomás, Podracká Ludmila, Eiberg Hans, Rittig Sør |
Novel haplotypes responsible for prenatal death in Nordic Red and Danish Jersey cattle. Journal of dairy science 2020 Mar . Wu Xiaoping, Mesbah-Uddin Md, Guldbrandtsen Bernt, Lund Mogens S, Sahana Gout |
Targeted next-generation sequencing for locally advanced prostate cancer in the Korean population. Investigative and clinical urology 2020 3 61 (2): 127-135. Suh Jungyo, Jeong Chang Wook, Choi Seongmin, Ku Ja Hyeon, Kim Hyeon Hoe, Kim Kwang Soo, Kwak Che |
HLA Class II Genotype Does Not Affect the Myelin Responsiveness of Multiple Sclerosis Patients. Cells 2020 12 9 (12): . Derdelinckx Judith, Nkansah Irene, Ooms Naomi, Van Bruggen Laura, Emonds Marie-Paule, Daniëls Liesbeth, Reynders Tatjana, Willekens Barbara, Cras Patrick, Berneman Zwi N, Cools Nathal |
A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders. Current Alzheimer research 2020 Nov . El Bitar Fadia, Al Sudairy Nourah, Qadi Najeeb, Al Rajeh Saad, Alghamdi Fatimah, Al Amari Hala, Al Dawsari Ghadeer, Alsubaie Sahar, Al Sudairi Mishael, Abdulaziz Sara, Al Tassan Na |
Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent. Frontiers in genetics 2020 11 11 558762. Joslin Shannon E K, Durbin-Johnson Blythe P, Britton Monica, Settles Matthew L, Korf Ian, Lemay Danielle |
Insertion variants missing in the human reference genome are widespread among human populations. BMC biology 2020 11 18 (1): 167. Lee Young-Gun, Lee Jin-Young, Kim Junhyong, Kim Young-Jo |
Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.
PloS one 2021 9 16 (9): e0247287. Ashvetiya Tamara, Fan Sherry X, Chen Yi-Ju, Williams Charles H, O'Connell Jeffery R, Perry James A, Hong Charles |
Genetic Susceptibility for Low Testosterone in Men and Its Implications in Biology and Screening: Data from the UK Biobank.
European urology open science 2021 Jul 29 36-46. Fantus Richard J, Na Rong, Wei Jun, Shi Zhuqing, Resurreccion W Kyle, Halpern Joshua A, Franco Omar, Hayward Simon W, Isaacs William B, Zheng S Lilly, Xu Jianfeng, Helfand Brian |
Associations of Genetic Polymorphisms and Neuroimmune Markers With Some Parameters of Frontal Lobe Dysfunction in Schizophrenia. Frontiers in psychiatry 2021 12 655178. Morozova Anna, Zorkina Yana, Pavlov Konstantine, Pavlova Olga, Abramova Olga, Ushakova Valeria, Mudrak Alexander V, Zozulya Svetlana, Otman Irina, Sarmanova Zoya, Klyushnik Tatiana, Reznik Alexander, Kostyuk Georgiy, Chekhonin Vladim |
Associations of Serum Cytokine Levels and Interleukin-6-572C/G Polymorphism with Myelin Damage in Chinese Children with Autism Spectrum Disorder. Neuroscience 2021 Apr 465 95-104. Han Yu, Xiong Wenjuan, Liu Jiaxue, Dai Wei, Su Yuanyuan, Gao Lei, Wang Gengfu, Li Peiying, Zhang X |
[Specific features of immunological reactions in elderly and young patients with exacerbation of schizophrenia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2021 3 121 (2): 53-59. Klyushnik T P, Barkhatova A N, Sheshenin V S, Androsova L V, Zozulya S A, Otman I N, Pochueva V |
A novel c.1759T>G variant in follicle-stimulating hormone-receptor gene is concordant with male determination in the flathead grey mullet (Mugil cephalus). G3 (Bethesda, Md.) 2021 2 11 (2): . Curzon Arie Y, Dor Lior, Shirak Andrey, Meiri-Ashkenazi Iris, Rosenfeld Hana, Ron Micha, Seroussi Ey |
PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation. Journal of the American Heart Association 2021 11 10 (23): e023517. Guo Xiao-Juan, Qiu Xing-Biao, Wang Jun, Guo Yu-Han, Yang Chen-Xi, Li Li, Gao Ri-Feng, Ke Zun-Ping, Di Ruo-Min, Sun Yu-Min, Xu Ying-Jia, Yang Yi-Qi |
Influence of Genetic Polymorphisms on Clinical Outcomes of Glatiramer Acetate in Multiple Sclerosis Patients. Journal of personalized medicine 2021 Oct 11 (10): . Zarzuelo-Romero María José, Pérez-Ramírez Cristina, Cura Yasmín, Carrasco-Campos María Isabel, Marangoni-Iglecias Luciana María, Ramírez-Tortosa María Carmen, Jiménez-Morales Alber |
Prognostic Value of Copy Number Alteration Burden in Early-Stage Breast Cancer and the Construction of an 11-Gene Copy Number Alteration Model. Cancers 2022 9 14 (17): . Wang Dingyuan, Gao Songlin, Qian Haili, Yuan Peng, Zhang Bail |
Updated Genome-Wide Association Study of Intracranial Aneurysms by Genotype Correction and Imputation in Koreans. World neurosurgery 2022 Jul . Hong Eun Pyo, Kim Bong Jun, Youn Dong Hyuk, Lee Jae Jun, Jeon Hong Jun, Choi Hyuk Jai, Cho Yong Jun, Jeon Jin Pyeong, |
A Pex7 Deficient Mouse Series Correlates Biochemical and Neurobehavioral Markers to Genotype Severity-Implications for the Disease Spectrum of Rhizomelic Chondrodysplasia Punctata Type 1. Frontiers in cell and developmental biology 2022 7 10 886316. Fallatah Wedad, Cui Wei, Di Pietro Erminia, Carter Grace T, Pounder Brittany, Dorninger Fabian, Pifl Christian, Moser Ann B, Berger Johannes, Braverman Nancy |
Phase Ib study of anlotinib combined with TQB2450 in pretreated advanced biliary tract cancer and biomarker analysis. Hepatology (Baltimore, Md.) 2022 May . Zhou Jun, Sun Yongkun, Zhang Wen, Yuan Jiajia, Peng Zhi, Wang Wei, Gong Jifang, Yang Lin, Cao Yanshuo, Zhao Hong, Chen Chao, Wang Weifeng, Shen Lin, Zhou Aipi |
Investigation of the relationship between MBP gene polymorphisms and delayed encephalopathy after acute carbon monoxide poisoning. Neurotoxicology 2022 Dec . Zhang Fan, Zeng Jiao, Zhang Xiaoli, Gu Jiapeng, Han Yongkai, Zhang Ping, Li Wenqiang, Gu Renj |
Novel synthetic lethality drug target in urothelial bladder cancer based on MTAP genomic loss. Urologic oncology 2022 11 41 (2): 109.e15-109.e22. Basin Michael F, Bratslavsky Gennady, Nahhas Nathan, Basnet Alina, Goldberg Hanan, Necchi Andrea, Sokol Ethan S, Ramkissoon Shakti H, Huang Richard S P, Ross Jeffrey S, Jacob Joseph |
The kinetics of blast clearance are associated with copy number alterations in childhood B-cell acute lymphoblastic leukemia. Neoplasia (New York, N.Y.) 2022 10 35 100840. Urba?ska Zuzanna, Lejman Monika, Taha Joanna, Madzio Joanna, Ostrowska Kinga, Miarka-Walczyk Karolina, Wypyszczak Kamila, Styka Borys, Jakubowska Justyna, S?dek ?ukasz, Szczepa?ski Tomasz, Sta?czak Marcin, Fendler Wojciech, M?ynarski Wojciech, Pastorczak Aga |
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis. International journal of molecular sciences 2022 10 23 (19): . Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee |
Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor. Biomedicines 2022 1 10 (1): . Abondio Paolo, Sarno Stefania, Giuliani Cristina, Laganà Valentina, Maletta Raffaele, Bernardi Livia, Bruno Francesco, Colao Rosanna, Puccio Gianfranco, Frangipane Francesca, Borroni Barbara, Van Broeckhoven Christine, Luiselli Donata, Bruni Amal |
Astrocytic response mediated by the CLU risk allele inhibits OPC proliferation and myelination in a human iPSC model. Cell reports 2023 7 42 (8): 112841. Zhenqing Liu, Jianfei Chao, Cheng Wang, Guihua Sun, Daniel Roeth, Wei Liu, Xianwei Chen, Li Li, E Tian, Lizhao Feng, Hayk Davtyan, Mathew Blurton-Jones, Markus Kalkum, Yanhong S |
Marker-trait association analyses revealed major novel QTLs for grain yield and related traits in durum wheat. Frontiers in plant science 2023 2 13 1009244. Mulugeta Behailu, Tesfaye Kassahun, Ortiz Rodomiro, Johansson Eva, Hailesilassie Teklehaimanot, Hammenhag Cecilia, Hailu Faris, Geleta Mula |
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- Page last updated:Apr 22, 2024
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