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A prospective comparison of UroVysion FISH and urine cytology in bladder cancer detection.
BMC Cancer. 2017 Apr 7;17(1):247. doi: 10.1186/s12885-017-3227-3.
BMC Cancer. 2017.
PMID: 28388880
Free PMC article.
Frequency, molecular pathology and potential clinical significance of partial chromosome 3 aberrations in uveal melanoma.
Abdel-Rahman MH, Christopher BN, Faramawi MF, Said-Ahmed K, Cole C, McFaddin A, Ray-Chaudhury A, Heerema N, Davidorf FH.
Abdel-Rahman MH, et al. Among authors: mcfaddin a.
Mod Pathol. 2011 Jul;24(7):954-62. doi: 10.1038/modpathol.2011.51. Epub 2011 Apr 15.
Mod Pathol. 2011.
PMID: 21499235
Free PMC article.
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Dic(17;18)(p11.2;p11.2) is a recurring abnormality in chronic lymphocytic leukaemia associated with aggressive disease.
Woyach JA, Heerema NA, Zhao J, McFaddin A, Stark A, Lin TS, Andritsos LA, Blum KA, Flynn JM, Jones JA, Byrd JC.
Woyach JA, et al. Among authors: mcfaddin a.
Br J Haematol. 2010 Mar;148(5):754-9. doi: 10.1111/j.1365-2141.2009.08007.x. Epub 2009 Dec 16.
Br J Haematol. 2010.
PMID: 20015097
Free PMC article.
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Jumping translocations, a novel finding in chronic lymphocytic leukaemia.
Miller CR, Stephens D, Ruppert AS, Racke F, McFaddin A, Breidenbach H, Lin HJ, Waller K, Bannerman T, Jones JA, Woyach JA, Andritsos LA, Maddocks K, Zhao W, Lozanski G, Flynn JM, Grever M, Byrd JC, Heerema NA.
Miller CR, et al. Among authors: mcfaddin a.
Br J Haematol. 2015 Jul;170(2):200-7. doi: 10.1111/bjh.13422. Epub 2015 Apr 19.
Br J Haematol. 2015.
PMID: 25891862
Free PMC article.
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Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives.
Byers HM, Jacobson A, McFaddin AS, Ussakli CH, Newlin A, Stanich PP, More S, Hamblett A, Tait JF, Shirts B, Pritchard CC, Konnick EQ, Lockwood CM.
Byers HM, et al. Among authors: mcfaddin as.
JCO Precis Oncol. 2018 Aug 14;2:PO.18.00108. doi: 10.1200/PO.18.00108. eCollection 2018.
JCO Precis Oncol. 2018.
PMID: 32913991
Free PMC article.
No abstract available.
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Simultaneous germline and somatic sequencing in ovarian carcinoma: mutation rate and impact on clinical decision-making.
Jorge S, McFaddin AS, Doll KM, Pennington KP, Norquist BM, Bennett RL, Pritchard CC, Swisher EM.
Jorge S, et al. Among authors: mcfaddin as.
Gynecol Oncol. 2020 Mar;156(3):517-522. doi: 10.1016/j.ygyno.2019.12.010. Epub 2019 Dec 27.
Gynecol Oncol. 2020.
PMID: 31883735
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Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach.
Harrison SM, Dolinksy JS, Chen W, Collins CD, Das S, Deignan JL, Garber KB, Garcia J, Jarinova O, Knight Johnson AE, Koskenvuo JW, Lee H, Mao R, Mar-Heyming R, McFaddin AS, Moyer K, Nagan N, Rentas S, Santani AB, Seppälä EH, Shirts BH, Tidwell T, Topper S, Vincent LM, Vinette K, Rehm HL; ClinGen Sequence Variant Inter-Laboratory Discrepancy Resolution Working Group.
Harrison SM, et al. Among authors: mcfaddin as.
Hum Mutat. 2018 Nov;39(11):1641-1649. doi: 10.1002/humu.23643.
Hum Mutat. 2018.
PMID: 30311378
Free PMC article.
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