Keller MA - Search Results

1

Effect on gene expression of three allelic variants in GATA motifs of ABO, RHD, and RHCE regulatory elements.

Fennell K, Hoffman R, Yoshida K, Iwamoto S, Govender L, Vather K, Sookraj A, Jentsch U, Pambrun C, McAuley C, Keller MA, Ochoa-Garay G. Fennell K, et al. Among authors: keller ma. Transfusion. 2017 Nov;57(11):2804-2808. doi: 10.1111/trf.14299. Epub 2017 Aug 16. Transfusion. 2017. PMID: 28815618

2

RHCE variant allele: RHCE*ce254G,733G.

Keller JA, Horn T, Chiappa C, Melland C, Vietz C, Castilho L, Keller MA. Keller JA, et al. Among authors: keller ma. Immunohematology. 2014;30(3):121-2. Immunohematology. 2014. PMID: 25695437

3

Financial implications of RHD genotyping of pregnant women with a serologic weak D phenotype.

Kacker S, Vassallo R, Keller MA, Westhoff CM, Frick KD, Sandler SG, Tobian AA. Kacker S, et al. Among authors: keller ma. Transfusion. 2015 Sep;55(9):2095-103. doi: 10.1111/trf.13074. Epub 2015 Mar 21. Transfusion. 2015. PMID: 25808011 Free PMC article.

4

Strategies to identify candidates for D variant genotyping.

Luo X, Keller MA, James I, Grant M, Liu S, Massey KS, Czulewicz A, Nance S, Li Y. Luo X, et al. Among authors: keller ma. Blood Transfus. 2018 May;16(3):293-301. doi: 10.2450/2017.0274-16. Epub 2017 Apr 5. Blood Transfus. 2018. PMID: 28488958 Free PMC article.

5

Novel mutations in KLF1 encoding the In(Lu) phenotype reflect a diversity of clinical presentations.

Keller J, Vege S, Horn T, Keller MA, Leger RM, Aeschlimann J, Lomas-Francis C, Westhoff CM. Keller J, et al. Among authors: keller ma. Transfusion. 2018 Jan;58(1):196-199. doi: 10.1111/trf.14378. Epub 2017 Oct 19. Transfusion. 2018. PMID: 29047116

6

RH genotype matching for transfusion support in sickle cell disease.

Chou ST, Evans P, Vege S, Coleman SL, Friedman DF, Keller M, Westhoff CM. Chou ST, et al. Blood. 2018 Sep 13;132(11):1198-1207. doi: 10.1182/blood-2018-05-851360. Epub 2018 Jul 19. Blood. 2018. PMID: 30026182 Free article.

7

Experience with RHD*weak D type 4.0 in the USA.

Westhoff CM, Nance S, Lomas-Francis C, Keller M, Chou ST. Westhoff CM, et al. Blood Transfus. 2019 Mar;17(2):91-93. doi: 10.2450/2018.0114-18. Epub 2018 Jul 6. Blood Transfus. 2019. PMID: 30036180 Free PMC article. No abstract available.

8

It's time to phase out "serologic weak D phenotype" and resolve D types with RHD genotyping including weak D type 4.

Flegel WA, Denomme GA, Queenan JT, Johnson ST, Keller MA, Westhoff CM, Katz LM, Delaney M, Vassallo RR, Simon CD, Sandler SG. Flegel WA, et al. Among authors: keller ma. Transfusion. 2020 Apr;60(4):855-859. doi: 10.1111/trf.15741. Epub 2020 Mar 12. Transfusion. 2020. PMID: 32163599 Free PMC article. No abstract available.

9

New ABO intron 1 variant alleles.

Fennell K, Keller MA, Villa MA, Paccapelo C, Kucerakova M, Rosochova J, Clemente DosSantos C, Brackney L, Lee CJ, Metcalf R, Crovetti G, Barbieri M, Travali S, Barrotta G, Giuca G, Guerra LE, Ochoa-Garay G. Fennell K, et al. Among authors: keller ma. Immunohematology. 2021;37(4):178-184. doi: 10.21307/immunohematology-2021-029. Immunohematology. 2021. PMID: 34964317

10

A model for integrating molecular-based testing in transfusion services.

Sandler SG, Horn T, Keller J, Langeberg A, Keller MA. Sandler SG, et al. Among authors: keller j, keller ma. Blood Transfus. 2016 Nov;14(6):566-572. doi: 10.2450/2015.0070-15. Epub 2015 Sep 3. Blood Transfus. 2016. PMID: 26509823 Free PMC article.

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