Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 197 Records) |
Query Trace: RHD[original query] |
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Identification of RHD allelic variants discovered by atypical typing results on the NEO/Echo platforms. Immunohematology 2021 12 37 (4): 165-170. Hudgins J P, Matsushita C, Tuma C W, O'Brien L, Shulman I |
The importance of being heterozygote: effects of RHD-genotype-sex interaction on the physical and mental health of a non-clinical population. Scientific reports 2021 Nov 11 (1): 21960. Flegr Jaroslav, P?íplatová Lenka, Hlavá?ová Jana, Šebánková Blanka, Ž?árský Emanuel, Ka?ková Šár |
Molecular red cell genotyping of rare blood donors in South Africa to enhance rare donor-patient blood matching. African journal of laboratory medicine 2021 10 (1): 1400. Govender Lavendri, Prakashchandra Rosaley D, Pillay Pavitra, Jentsch U |
Molecular blood group screening in Omani blood donors. Vox sanguinis 2021 10 117 (3): 424-430. Al-Riyami Arwa Z, Al Hinai Dina, Al-Rawahi Mohammed, Al-Hosni Saif, Al-Zadjali Shoaib, Al-Marhoobi Ali, Al-Khabori Murtadha, Al-Riyami Hamad, Denomme Gregory |
Molecular basis of RhD-negative phenotype in North Indian blood donor population. The Indian journal of medical research 2022 8 155 (2): 286-292. Khetan Dheeraj, Shukla Jai Shukla, Chaudhary Rajendra |
RHD 1227 A and hybrid Rhesus box analysis in Thai RhD+ and RhD- blood donors: Prevalence, RHD zygosity, and molecular screening. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2022 7 61 (6): 103496. Simtong Piyapong, Phothi Rattanaporn, Puapairoj Chintana, Leelayuwat Chanvit, Romphruk Amornrat |
From the investigation of RHD-CE hybrid genes to the recognition of RHCE variants and RHD zygosity. Expanding the analysis by QMPSF in Brazilian donors and in patients with sickle cell disease. Blood transfusion = Trasfusione del sangue 2022 May . de Paula Vendrame Tatiane A, Arnoni Carine P, Latini Flavia R M, Pereira Cortez Afonso J, Bénech Caroline, Fichou Yann, Castilho Lili |
The Frequency of Rh Phenotype and Its Probable Genotype. Cureus 2022 7 14 (6): e25775. Tariq Faryal, Ashfaq Javeria, Ahmed Rehana, Fatima Naveena, Ahmed Yumna, Borhany Muni |
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years. Vox sanguinis 2022 5 117 (7): 949-957. Ye Luyi, Li Minghao, Yang Qixiu, Zhu Ziy |
The genomic landscape of blood groups in Indigenous Australians in remote communities. Transfusion 2022 4 62 (5): 1110-1120. Jadhao Sudhir, Hoy Wendy, Lee Simon, Patel Hardip R, McMorran Brendan J, Flower Robert L, Nagaraj Shivashankar |
Confirmed non-invasive prenatal testing for foetal Rh blood group genotyping along with bi-allelic short insertion/deletion polymorphisms as a positive internal control. Transfusion medicine (Oxford, England) 2022 3 32 (2): 141-152. Armstrong-Fisher Sylvia, Koushki Khadijeh, Mashayekhi Kazem, Urbaniak Stanislaw J, van der Schoot Ellen, Varzi Ali Mohamm |
PSRC1 May Affect Coronary Artery Disease Risk by Altering CELSR2, PSRC1, and SORT1 Gene Expression and Circulating Granulin and Apolipoprotein B Protein Levels. Frontiers in cardiovascular medicine 2022 3 9 763015. Chai Tianci, Wang Zhisheng, Yang Xiaojie, Qiu Zhihuang, Chen Liangw |
RHD exon 5, 7 and 10 targeted non-invasive prenatal screening of fetal Rhesus-D (RhD) in selected RhD negative pregnant women in Ethiopia. PloS one 2022 3 17 (3): e0265583. Niguse Birhanu, Ermias Mihertab, Berhanu Solomon, Abayneh Lemma, Chakiso Bekele, Rather Riyaz Ahm |
Emphasizing the link between blood types in multi-ethnic disparities and COVID-19 infection in Makkah, Saudi Arabia. Saudi medical journal 2022 2 43 (2): 177-186. Nasif Wesam A, Ali Abeer S E, Khogeer Asim A, Mukhtar Mohammed H, NourEldein Mohamed M, Shebly Ahmed Y, Alqahtani Shmukh H, Alnashri Yahya A, Khouj Ghidaa E, Gadah Ziyad I, Althubiti Mohammad |
A study on the association of IL-10 promoter polymorphisms with rheumatic heart disease in Turkish female patients. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2022 Jan 50 (1): 14-21. Akadam-Teke Ay?egül Ba?ak, Teker Erh |
Investigating anti-D in an individual with the weak D type 2 genotype. Immunohematology 2022 10 38 (3): 77-81. Phou S, Nguyen N, Revilla J, Rodberg K, Gibb D R, Pepkowitz S H, Klapper E |
Frequency and characterization of RHD and RHCE variants in the Noir Marron population from French Guiana. Transfusion 2022 10 62 (12): 2631-2638. Laget Laurine, Izard Caroline, Durieux-Roussel Elisabeth, Filosa Lugdivine, Bailly Pascal, Mazières Stéphane, Chiaroni Jacqu |
Comparative analysis of antigen coding genes in 15 red cell blood group systems of Yunnan Yi nationality in China: A cross-sectional study. Health science reports 2022 Nov 5 (6): e891. He Kun-Hua, Xu Lu-Qiong, Hu Ying-Feng, Xu Yin-Xia, Zhao Yu, Bao Jing-Yan, Wang Bu-Qia |
Association of HLA-DRB1 alleles with anti-D alloimmunization in RhD negative pregnant women in India. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2023 9 103789. Ashish Jain, Ratti Ram Sharma, Ranjana W Minz, Subhas Chandra Sa |
Characterization of pediatric transfusion-dependent thalassemia patients in a large academic center. Journal of clinical laboratory analysis 2023 9 e24962. Dorsa Zarrabian, Mirette Han |
Evidence that donors with variant RH genotypes are associated with unexpected Rh antibodies. Transfusion 2023 9 . Julie Kirkegaard, Lynsi Rahorst, Anna Burgos, Lejla Music Aplenc, Nazia Tabassum Iqbal, Sunitha Vege, Christine Lomas Francis, Connie M Westho |
Association of HLA class II DR/DQ alleles in children and adolescents with rheumatic heart disease from a tertiary care centre in North India. Indian heart journal 2023 7 . Anbarasan A, Dinesh Kumar, Rakesh Deepak, Dheeraj Deo Bhatt, Lata Kumari, Praveen Arumugam, Kawaldeep Kaur, Likhith Kumar |
The Impact of ACE Gene Variants on Acute-Phase Reactants in Children with Rheumatic Heart Disease. Diagnostics (Basel, Switzerland) 2023 5 13 (10): . Abdulhadi H Almazroea, Sondos Yousef, Salma M S Ahmad, Hanin N AlHiraky, Amal Al-Haidose, Atiyeh M Abdall |
Prevalence of weak D phenotypes in the general population of Québec, Canada: A focus on weak D type 42. Vox sanguinis 2023 5 . Mathieu Drouin, Samuel Rochette, Maryse St-Louis, Antoine Lewin, Josée Laganiè |
Cases of RhD variants RhD*DAU2/DAU6 and RhD*weak D type 4.1 in pregnant women in Saudi Arabia. Acta bio-medica : Atenei Parmensis 2023 3 94 (S1): e2023080. Owaidah Amani, Aljuhani Khadijah, Albasri Jasem, Alsulmi Eman, Alsaihati Taibah, Alzahrani Fais |
Transfusion support for a patient with alloanti-D and the RHD*DV.1 allele. Clinica chimica acta; international journal of clinical chemistry 2023 2 541 117268. Jiang Luxi, Du Yaoqiang, Hao Ke, Mei Menghan, Li Yu, Chen Bingyu, Xie Yiw |
Polymorphisms in the promoter regions of RHD and RHCE genes in the Chinese Han population. Vox sanguinis 2023 10 . Lin-Nan Shao, Zi-Wei Zheng, Shi-Hang Zhou, Shu-Ting Zhang, Wen-Qian Song, Yue-Xin Xia, Xiao-Hua Lia |
Estimating the serological underrecognition of patients with weak or partial RHD variants. Transfusion 2024 4 . Glenn Ramsey, Christina M Barrite |
[Molecular biology analysis of 2 rare RhD variant individuals with RHD*DEL37]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2024 4 56 (2): 352-356. Peng Wang, Ziyao Yang, Meng Wang, Wei Wang, Aizhi |
[Establishment of a genotyping method for the junior blood group and identification of a rare blood type with partial DVI.3 and Jr(a-)]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 1 41 (1): 52-58. Shuang Liang, Chunyan Mo, Xiaoyang Liu, Yanli Ji, Yanlian Liang, Fan Wu, Guangping Luo, Yuqing |
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- Page last updated:Apr 22, 2024
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