-
1
-
-
67650483405
-
Set-up and routine use of a database of 10555 genotyped blood donors to facilitate the screening of compatible blood components for alloimmunized patients
-
Perrault J., Lavoie J., Painchaud P., Côté M., Constanzo-Yanez J., Côté R., et al. Set-up and routine use of a database of 10555 genotyped blood donors to facilitate the screening of compatible blood components for alloimmunized patients. Vox Sang 2009, 97:61-68.
-
(2009)
Vox Sang
, vol.97
, pp. 61-68
-
-
Perrault, J.1
Lavoie, J.2
Painchaud, P.3
Côté, M.4
Constanzo-Yanez, J.5
Côté, R.6
-
2
-
-
84858276939
-
High-throughput multiplex PCR genotyping for 35 red blood cell antigens in blood donors
-
Jungbauer J., Hobel C.M., Schwartz D.W.M., Mayr W.R. High-throughput multiplex PCR genotyping for 35 red blood cell antigens in blood donors. Vox Sang 2012, 102:234-242.
-
(2012)
Vox Sang
, vol.102
, pp. 234-242
-
-
Jungbauer, J.1
Hobel, C.M.2
Schwartz, D.W.M.3
Mayr, W.R.4
-
3
-
-
84883778347
-
Prospects for the provision of genotyped blood for transfusion
-
Denomme G. Prospects for the provision of genotyped blood for transfusion. Br J Haematol 2013, 163:3-9.
-
(2013)
Br J Haematol
, vol.163
, pp. 3-9
-
-
Denomme, G.1
-
4
-
-
70349553955
-
Blood group genotyping: from patient to high-throughput donor screening
-
Veldhuisen B., van der Schoot C.E., de Haas M. Blood group genotyping: from patient to high-throughput donor screening. Vox Sang 2009, 97:198-206.
-
(2009)
Vox Sang
, vol.97
, pp. 198-206
-
-
Veldhuisen, B.1
van der Schoot, C.E.2
de Haas, M.3
-
5
-
-
84868213735
-
Challenges of alloimmunisation in patients with haemoglobinopathies
-
Chou S.T., Liem R.I., Thompson A.A. Challenges of alloimmunisation in patients with haemoglobinopathies. Br J Haematol 2012, 159(4):394-404.
-
(2012)
Br J Haematol
, vol.159
, Issue.4
, pp. 394-404
-
-
Chou, S.T.1
Liem, R.I.2
Thompson, A.A.3
-
6
-
-
73649090025
-
High-throughput red blood cell antigen genotyping using a nanofluidic real-time polymerase chain reaction platform
-
Hopp K., Weber K., Bellissimo D., Johnson S.T., Pietz B. High-throughput red blood cell antigen genotyping using a nanofluidic real-time polymerase chain reaction platform. Transfusion 2010, 50:40-46.
-
(2010)
Transfusion
, vol.50
, pp. 40-46
-
-
Hopp, K.1
Weber, K.2
Bellissimo, D.3
Johnson, S.T.4
Pietz, B.5
-
7
-
-
84893161498
-
Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy
-
Haer-Wigman L., Ji Y., Lodén M., de Haas M., van der Schoot E., Veldhuisen B. Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy. Transfusion 2013, 53:2899-2909.
-
(2013)
Transfusion
, vol.53
, pp. 2899-2909
-
-
Haer-Wigman, L.1
Ji, Y.2
Lodén, M.3
de Haas, M.4
van der Schoot, E.5
Veldhuisen, B.6
-
8
-
-
84872232876
-
Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry-based blood group genotyping - the alternative approach
-
Gassner C., Meyer S., Frey B.M., Vollmert C. Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry-based blood group genotyping - the alternative approach. Transfus Med Rev 2013, 27:2-9.
-
(2013)
Transfus Med Rev
, vol.27
, pp. 2-9
-
-
Gassner, C.1
Meyer, S.2
Frey, B.M.3
Vollmert, C.4
-
9
-
-
74549187471
-
A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein
-
Tilley L., Green C., Poole J., Gaskell A., Ridgwell K., Burton N.M., et al. A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein. Vox Sang 2010, 98:151-159.
-
(2010)
Vox Sang
, vol.98
, pp. 151-159
-
-
Tilley, L.1
Green, C.2
Poole, J.3
Gaskell, A.4
Ridgwell, K.5
Burton, N.M.6
-
10
-
-
84882326962
-
KETI, a novel high incidence antigen in the Kell blood group system: a serological and molecular study
-
Karamatic-Crew V., Poole J., Bullock T., Regan P., Burton N., Daniels G. KETI, a novel high incidence antigen in the Kell blood group system: a serological and molecular study. Vox Sang 2011, 101(suppl. 1):19.
-
(2011)
Vox Sang
, vol.101
, Issue.SUPPL. 1
, pp. 19
-
-
Karamatic-Crew, V.1
Poole, J.2
Bullock, T.3
Regan, P.4
Burton, N.5
Daniels, G.6
-
11
-
-
84900480541
-
Two novel RhD variants that share the weak D type 4 mutations
-
Grimsley S., Skidmore I., Lee E., Thornton N., Daniels G. Two novel RhD variants that share the weak D type 4 mutations. Transfus Med 2013, 23(suppl. 2):65.
-
(2013)
Transfus Med
, vol.23
, Issue.SUPPL. 2
, pp. 65
-
-
Grimsley, S.1
Skidmore, I.2
Lee, E.3
Thornton, N.4
Daniels, G.5
-
12
-
-
84874687425
-
Developing genome and exome sequencing for candidate gene identification in inherited disorders
-
Coonrod E.M., Durtschi J.D., Margraf R.L., Voelkerding K.V. Developing genome and exome sequencing for candidate gene identification in inherited disorders. Arch Pathol Lab Med 2013, 137:415-433.
-
(2013)
Arch Pathol Lab Med
, vol.137
, pp. 415-433
-
-
Coonrod, E.M.1
Durtschi, J.D.2
Margraf, R.L.3
Voelkerding, K.V.4
-
13
-
-
84887611816
-
Next-generation sequencing in the clinic: promises and challenges
-
Xuan J., Yu Y., Qing T., Guo L., Shi L. Next-generation sequencing in the clinic: promises and challenges. Cancer Lett 2013, 340:284-295.
-
(2013)
Cancer Lett
, vol.340
, pp. 284-295
-
-
Xuan, J.1
Yu, Y.2
Qing, T.3
Guo, L.4
Shi, L.5
-
14
-
-
84862777457
-
Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities
-
Lin X., Tang W., Ahmad S., Lu J., Colby C., Zhu J., et al. Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities. Hear Res 2012, 288:67-76.
-
(2012)
Hear Res
, vol.288
, pp. 67-76
-
-
Lin, X.1
Tang, W.2
Ahmad, S.3
Lu, J.4
Colby, C.5
Zhu, J.6
-
15
-
-
84872596130
-
Next generation diagnostics in inherited arrhythmia syndromes - a comparison of two approaches
-
Ware J., John S., Roberts A.M., Buchan R., Gong S., Peters N.S., et al. Next generation diagnostics in inherited arrhythmia syndromes - a comparison of two approaches. J Cardiovasc Transl Res 2013, 6:94-103.
-
(2013)
J Cardiovasc Transl Res
, vol.6
, pp. 94-103
-
-
Ware, J.1
John, S.2
Roberts, A.M.3
Buchan, R.4
Gong, S.5
Peters, N.S.6
-
16
-
-
84872250896
-
16th IHIW: review of HLA typing by NGS
-
De Santis D., Dinauer D., Duke J., Erlich H.A., Holcomb C.L., Lind C., et al. 16th IHIW: review of HLA typing by NGS. Int J Immunogenet 2013, 40:72-76.
-
(2013)
Int J Immunogenet
, vol.40
, pp. 72-76
-
-
De Santis, D.1
Dinauer, D.2
Duke, J.3
Erlich, H.A.4
Holcomb, C.L.5
Lind, C.6
-
17
-
-
84875689644
-
Rapid, scalable and highly automated HLA genotyping using next-generation sequencing: a transition from research to diagnostics
-
Danzer M., Niklas N., Stabentheiner S., Hofer K., Pröll J., Stückler C., et al. Rapid, scalable and highly automated HLA genotyping using next-generation sequencing: a transition from research to diagnostics. BMC Genomics 2013, 14:221.
-
(2013)
BMC Genomics
, vol.14
, pp. 221
-
-
Danzer, M.1
Niklas, N.2
Stabentheiner, S.3
Hofer, K.4
Pröll, J.5
Stückler, C.6
-
18
-
-
84900502145
-
Next generation sequencing (NGS) for blood group genotyping
-
Fichou Y., Audrézet M.P., Guéguen P., Dupont I., James D., Le Maréchal C., et al. Next generation sequencing (NGS) for blood group genotyping. Vox Sang 2013, 105(suppl. 1):59.
-
(2013)
Vox Sang
, vol.105
, Issue.SUPPL. 1
, pp. 59
-
-
Fichou, Y.1
Audrézet, M.P.2
Guéguen, P.3
Dupont, I.4
James, D.5
Le Maréchal, C.6
-
19
-
-
84900467859
-
Comprehensive genotyping for Kell and Rh blood group systems by next-generation DNA sequencing
-
Halawani A.J., Altayar M.A., Kiernan M., Kaushik N., Reynolds A., Madgett T., et al. Comprehensive genotyping for Kell and Rh blood group systems by next-generation DNA sequencing. Transfus Med 2013, 23(suppl. 2):62.
-
(2013)
Transfus Med
, vol.23
, Issue.SUPPL. 2
, pp. 62
-
-
Halawani, A.J.1
Altayar, M.A.2
Kiernan, M.3
Kaushik, N.4
Reynolds, A.5
Madgett, T.6
-
20
-
-
84900501462
-
Next generation sequencing of ABO, Duffy and Kidd blood group genotyping
-
Altayer M., Halawani A., Kiernan M., Reynolds A., Kaushik N., Madgett T., et al. Next generation sequencing of ABO, Duffy and Kidd blood group genotyping. Transfus Med 2013, 23(suppl. 2):62.
-
(2013)
Transfus Med
, vol.23
, Issue.SUPPL. 2
, pp. 62
-
-
Altayer, M.1
Halawani, A.2
Kiernan, M.3
Reynolds, A.4
Kaushik, N.5
Madgett, T.6
-
21
-
-
84900467548
-
International society of blood transfusion working party on red cell immunogenetics and blood group terminology: Cancun report (2012)
-
[ahead of print]
-
Storry J.R., Castilho L., Daniels G., Flegel W.A., Garratty G., de Haas M., et al. International society of blood transfusion working party on red cell immunogenetics and blood group terminology: Cancun report (2012). Vox Sang 2014, http://dx.doi.org/10.1111/vox.12127, [ahead of print].
-
(2014)
Vox Sang
-
-
Storry, J.R.1
Castilho, L.2
Daniels, G.3
Flegel, W.A.4
Garratty, G.5
de Haas, M.6
-
22
-
-
84878603453
-
Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype
-
Storry J.R., Jöud M., Christophersen M.K., Thuresson B., Åkerström B., Sojka B.N., et al. Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype. Nat Genet 2013, 45(5):537-541.
-
(2013)
Nat Genet
, vol.45
, Issue.5
, pp. 537-541
-
-
Storry, J.R.1
Jöud, M.2
Christophersen, M.K.3
Thuresson, B.4
Åkerström, B.5
Sojka, B.N.6
-
23
-
-
84878539656
-
SMIM1 underlies the Vel blood group and influences red blood cell traits
-
Cvejic A., Haer-Wigman L., Stephens J.C., Kostadima M., Smethurst P.A., Frontini M., et al. SMIM1 underlies the Vel blood group and influences red blood cell traits. Nat Genet 2013, 45:542-545.
-
(2013)
Nat Genet
, vol.45
, pp. 542-545
-
-
Cvejic, A.1
Haer-Wigman, L.2
Stephens, J.C.3
Kostadima, M.4
Smethurst, P.A.5
Frontini, M.6
-
24
-
-
84877617414
-
Disruption of SMIM1 causes the Vel-blood type
-
Ballif B.A., Helias V., Peyrard T., Menanteau C., Saison C., Lucien N., et al. Disruption of SMIM1 causes the Vel-blood type. EMBO Mol Med 2013, 5:751-761.
-
(2013)
EMBO Mol Med
, vol.5
, pp. 751-761
-
-
Ballif, B.A.1
Helias, V.2
Peyrard, T.3
Menanteau, C.4
Saison, C.5
Lucien, N.6
-
25
-
-
84904470443
-
A new blood group antigen is defined by anti-CD59, detected in a CD59-deficient patient
-
[ahead of print]
-
Anliker M., von Zabern I., Höchsmann B., Kyrieleis H., Dohna-Schwake C., Flegel W.A., et al. A new blood group antigen is defined by anti-CD59, detected in a CD59-deficient patient. Transfusion 2014, [ahead of print]. 10.1111/trf.12531.
-
(2014)
Transfusion
-
-
Anliker, M.1
von Zabern, I.2
Höchsmann, B.3
Kyrieleis, H.4
Dohna-Schwake, C.5
Flegel, W.A.6
-
26
-
-
84872613979
-
International reference reagents to standardise blood group genotyping: evaluation of candidate preparations in an international collaborative study
-
Boyle J., Thorpe S.J., Hawkins J.R., Lockie C., Fox B., Matejtschuk P., et al. International reference reagents to standardise blood group genotyping: evaluation of candidate preparations in an international collaborative study. Vox Sang 2013, 104:144-152.
-
(2013)
Vox Sang
, vol.104
, pp. 144-152
-
-
Boyle, J.1
Thorpe, S.J.2
Hawkins, J.R.3
Lockie, C.4
Fox, B.5
Matejtschuk, P.6
-
27
-
-
84865591846
-
A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers
-
Quail M.A., Smith M., Coupland P., Otto T.D., Harris S.R., Connor T.R., et al. A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers. BMC Genomics 2012, 13:341.
-
(2012)
BMC Genomics
, vol.13
, pp. 341
-
-
Quail, M.A.1
Smith, M.2
Coupland, P.3
Otto, T.D.4
Harris, S.R.5
Connor, T.R.6
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