Publications:

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RHD Genotyping of Rh-Negative and Weak D Phenotype among Blood Donors in Southeast Iran.

International Journal Of Hematology-Oncology And Stem Cell Research

Sadeghi-Bojd, Younes Y; Amirizadeh, Naser N; Oodi, Arezoo A

Publication Date: 2021-10-01

Variant appearance in text: RHD: 667T>G

PubMed Link: 35291662

Variant Present in the following documents:

• Main text
• IJHOSCR-15-213.pdf

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RHD Genotypes in a Chinese Cohort of Pregnant Women.

Frontiers In Genetics

Zhang, Jianjun J; Zeng, Yan Y; Wang, Yuefeng Y; Fan, Jiaming J; Chen, Haijiang H; Yang, Dan D; Shi, Xiaoliang X; Xu, Hualin H; Fu, Zimu Z; Sheng, Fang F; Xuan, Jie J; Pan, Xiaoxi X; Zhang, Zhiming Z; Ai, Liping L; Zhang, Yue Y; Pan, Jingjing J; Zhao, Jing J; Wang, Mingming M

Publication Date: 2021

Variant appearance in text: RHD: 667T>G

PubMed Link: 34970297

Variant Present in the following documents:

• Main text
• fgene-12-752485.pdf

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Transfusion support during childbirth for a woman with anti-U and the RHD*weak D type 4.0 allele.

Immunohematology

Yin, Q Q; Srivastava, K K; Brust, D G DG; Flegel, W A WA

Publication Date: 2021-03

Variant appearance in text: RHD: Phe223Val; rs1053356

PubMed Link: 33962485

Variant Present in the following documents:

• Main text

View BVdb publication page

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High prevalence of serological weak D phenotype and preponderance of weak D type 4.0.1. genetic variant in a Nigerian population: implications for transfusion practice in a resource-limited setting.

Hematology, Transfusion And Cell Therapy

Maryam, Dauda Usman DU; Mukhtar, Isyaku Gwarzo IG; Yusuf, Aminu Abba AA; Salisu, Ahmed Ibrahim AI

Publication Date: 2022

Variant appearance in text: RHD: F223V

PubMed Link: 33744228

Variant Present in the following documents:

• Main text
• main.pdf

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Next-generation sequencing of 35 RHD variants in 16 253 serologically D- pregnant women in the Finnish population.

Blood Advances

Tammi, Silja M SM; Tounsi, Wajnat A WA; Sainio, Susanna S; Kiernan, Michele M; Avent, Neil D ND; Madgett, Tracey E TE; Haimila, Katri K

Publication Date: 2020-10-27

Variant appearance in text: RHD: Phe223Val

PubMed Link: 33057632

Variant Present in the following documents:

• Main text

View BVdb publication page

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Comprehensive Molecular Analysis of Serologically D-Negative and Weak/Partial D Phenotype in Thai Blood Donors.

Transfusion Medicine And Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie

Thongbut, Jairak J; Raud, Loann L; Férec, Claude C; Promwong, Charuporn C; Nuchnoi, Pornlada P; Fichou, Yann Y

Publication Date: 2020-02

Variant appearance in text: RHD: 667T>G; F223V

PubMed Link: 32110194

Variant Present in the following documents:

• Main text

View BVdb publication page

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First Korean Case of Partial D DBS-1.

Annals Of Laboratory Medicine

Choi, Sooin S; Yu, HongBi H; Cho, Duck D

Publication Date: 2020-07

Variant appearance in text: RHD: F223V

PubMed Link: 32067436

Variant Present in the following documents:

• Main text
• alm-40-337.pdf

View BVdb publication page

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Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping.

The Journal Of Molecular Diagnostics : Jmd

Volkova, Evgeniya E; Sippert, Emilia E; Liu, Meihong M; Mercado, Teresita T; Denomme, Gregory A GA; Illoh, Orieji O; Liu, Zhugong Z; Rios, Maria M; ,

Publication Date: 2019-05

Variant appearance in text: RHD: 667T>G

PubMed Link: 30872185

Variant Present in the following documents:

• Main text

View BVdb publication page

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A recurrent point mutation in PRKCA is a hallmark of chordoid gliomas.

Nature Communications

Rosenberg, Shai S; Simeonova, Iva I; Bielle, Franck F; Verreault, Maite M; Bance, Bertille B; Le Roux, Isabelle I; Daniau, Mailys M; Nadaradjane, Arun A; Gleize, Vincent V; Paris, Sophie S; Marie, Yannick Y; Giry, Marine M; Polivka, Marc M; Figarella-Branger, Dominique D; Aubriot-Lorton, Marie-Hélène MH; Villa, Chiara C; Vasiljevic, Alexandre A; Lechapt-Zalcman, Emmanuèle E; Kalamarides, Michel M; Sharif, Ariane A; Mokhtari, Karima K; Pagnotta, Stefano Maria SM; Iavarone, Antonio A; Lasorella, Anna A; Huillard, Emmanuelle E; Sanson, Marc M

Publication Date: 2018-06-18

Variant appearance in text: RHD: F223V

PubMed Link: 29915258

Variant Present in the following documents:

• 41467_2018_4622_MOESM6_ESM.xlsx, sheet 1

View BVdb publication page

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Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia.

Blood Advances

Chou, Stella T ST; Flanagan, Jonathan M JM; Vege, Sunitha S; Luban, Naomi L C NLC; Brown, R Clark RC; Ware, Russell E RE; Westhoff, Connie M CM

Publication Date: 2017-08-08

Variant appearance in text: RHD: 667T>G

PubMed Link: 29296782

Variant Present in the following documents:

• Main text

View BVdb publication page

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Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.

Transfusion

Ouchari, Mouna M; Srivastava, Kshitij K; Romdhane, Houda H; Jemni Yacoub, Saloua S; Flegel, Willy Albert WA

Publication Date: 2018-02

Variant appearance in text: RHD: F223V

PubMed Link: 29193104

Variant Present in the following documents:

• Main text

View BVdb publication page

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Single Molecule Fluorescence Microscopy and Machine Learning for Rhesus D Antigen Classification.

Scientific Reports

Borgmann, Daniela M DM; Mayr, Sandra S; Polin, Helene H; Schaller, Susanne S; Dorfer, Viktoria V; Obritzberger, Lisa L; Endmayr, Tanja T; Gabriel, Christian C; Winkler, Stephan M SM; Jacak, Jaroslaw J

Publication Date: 2016-09-01

Variant appearance in text: RHD: 667T>G; F223V

PubMed Link: 27580632

Variant Present in the following documents:

• Main text
• srep32317.pdf

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The DAU cluster: a comparative analysis of 18 RHD alleles, some forming partial D antigens.

Transfusion

Srivastava, Kshitij K; Polin, Helene H; Sheldon, Sherry Lynne SL; Wagner, Franz Friedrich FF; Grabmer, Christoph C; Gabriel, Christian C; Denomme, Gregory Andrew GA; Flegel, Willy Albert WA

Publication Date: 2016-10

Variant appearance in text: RHD: Phe223Val

PubMed Link: 27480171

Variant Present in the following documents:

• Main text

View BVdb publication page

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GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics

Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J

Publication Date: 2015-07-25

Variant appearance in text: RHD: F223V

PubMed Link: 26206375

Variant Present in the following documents:

• 12859_2015_673_MOESM1_ESM.xls, sheet 5

View BVdb publication page

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Whole-genome sequencing of the world's oldest people.

Plos One

Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK

Publication Date: 2014

Variant appearance in text: RHD: F223V; rs1053356

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

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Weak D in the Tunisian population.

Blood Transfusion = Trasfusione Del Sangue

Ouchari, Mouna M; Romdhane, Houda H; Chakroun, Taher T; Abdelkefi, Saida S; Houissa, Batoul B; Hmida, Slama S; Yacoub, Saloua Jemni SJ

Publication Date: 2015-04

Variant appearance in text: RHD: F223V

PubMed Link: 25369614

Variant Present in the following documents:

• Main text

View BVdb publication page

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RHD PCR of D-Negative Blood Donors.

Transfusion Medicine And Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie

Wagner, Franz F FF

Publication Date: 2013-06

Variant appearance in text: RHD: F223V

PubMed Link: 23922542

Variant Present in the following documents:

• Main text

View BVdb publication page

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RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.

Transfusion

Westhoff, Connie M CM; Vege, Sunitha S; Horn, Trina T; Hue-Roye, Kim K; Halter Hipsky, Christine C; Lomas-Francis, Christine C; Reid, Marion E ME

Publication Date: 2013-11

Variant appearance in text: RHD: Phe223Val

PubMed Link: 23772606

Variant Present in the following documents:

• Main text

View BVdb publication page

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Red cells from the original JAL+ proband are also DAK+ and STEM+.

Vox Sanguinis

Hue-Roye, K K; Reid, M E ME; Westhoff, C M CM; Lomas-Francis, C C

Publication Date: 2011-07

Variant appearance in text: RHD: Phe223Val

PubMed Link: 21477150

Variant Present in the following documents:

• Main text

View BVdb publication page

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DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.

Transfusion

Westhoff, Connie M CM; Vege, Sunitha S; Halter-Hipsky, Christine C; Whorley, Trina T; Hue-Roye, Kim K; Lomas-Francis, Christine C; Reid, Marion E ME

Publication Date: 2010-06

Variant appearance in text: RHD: Phe223Val

PubMed Link: 20088832

Variant Present in the following documents:

• Main text

View BVdb publication page

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RHD allele distribution in Africans of Mali.

Bmc Genetics

Wagner, Franz F FF; Moulds, Joann M JM; Tounkara, Anatole A; Kouriba, Bourema B; Flegel, Willy A WA

Publication Date: 2003-09-24

Variant appearance in text: RHD: F223V

PubMed Link: 14505497

Variant Present in the following documents:

• Main text
• 1471-2156-4-14.pdf

View BVdb publication page

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RHD positive haplotypes in D negative Europeans.

Bmc Genetics

Wagner, F F FF; Frohmajer, A A; Flegel, W A WA

Publication Date: 2001

Variant appearance in text: RHD: F223V

PubMed Link: 11495631

Variant Present in the following documents:

• Main text
• 1471-2156-2-10.pdf

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