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Items: 1 to 50 of 57

1.

Impaired transmissibility of atypical prions from genetic CJDG114V.

Cali I, Mikhail F, Qin K, Gregory C, Solanki A, Martinez MC, Zhao L, Appleby B, Gambetti P, Norstrom E, Mastrianni JA.

Neurol Genet. 2018 Aug 7;4(4):e253. doi: 10.1212/NXG.0000000000000253. eCollection 2018 Aug.

2.

A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literature.

Upadia J, Philips JB 3rd, Robin NH, Lose EJ, Mikhail FM.

Clin Case Rep. 2018 Feb 14;6(4):612-616. doi: 10.1002/ccr3.1298. eCollection 2018 Apr.

3.

Therapy-associated myelodysplastic syndrome with monosomy 7 arising in a Muir-Torre Syndrome patient carrying SETBP1 mutation.

Ullman D, Baumgartner E, Wnukowski N, Koenig G, Mikhail FM, Pavlidakey P, Peker D.

Mol Clin Oncol. 2018 Feb;8(2):306-309. doi: 10.3892/mco.2017.1532. Epub 2017 Dec 8.

4.

Malignant Ewing-Like Neoplasm With an EWSR1-KLF15 Fusion: At the Crossroads of a Myoepithelial Carcinoma and a Ewing-Like Sarcoma. A Case Report With Treatment Options.

Stevens TM, Qarmali M, Morlote D, Mikhail FM, Swensen J, Gatalica Z, Siegal GP, Conry RM.

Int J Surg Pathol. 2018 Aug;26(5):440-447. doi: 10.1177/1066896918755009. Epub 2018 Feb 1.

PMID:
29390927
5.

Diagnostic and Prognostic Utility of Fluorescence In situ Hybridization (FISH) Analysis in Acute Myeloid Leukemia.

Gonzales PR, Mikhail FM.

Curr Hematol Malig Rep. 2017 Dec;12(6):568-573. doi: 10.1007/s11899-017-0426-6. Review.

PMID:
29064023
6.

Concomitant imatinib and ibrutinib in a patient with chronic myelogenous leukemia and chronic lymphocytic leukemia.

Shea LK, Mikhail FM, Forero-Torres A, Davis RS.

Clin Case Rep. 2017 Apr 24;5(6):899-901. doi: 10.1002/ccr3.974. eCollection 2017 Jun.

7.

Overview of Genetic Diagnosis in Cancer.

Korf BR, Mikhail FM.

Curr Protoc Hum Genet. 2017 Apr 6;93:10.1.1-10.1.9. doi: 10.1002/cphg.36. Review.

PMID:
28384400
8.

An adolescent with large cell calcifying sertoli cell tumor of the testis and undiagnosed Carney Complex: A case report.

Rosenblum F, Koenig RG, Mikhail FM, Porterfield JR, Nix JW, Eltoum IA.

Diagn Cytopathol. 2017 Jul;45(7):634-639. doi: 10.1002/dc.23700. Epub 2017 Mar 9.

PMID:
28276158
9.

Enhanced targeting of CML stem and progenitor cells by inhibition of porcupine acyltransferase in combination with TKI.

Agarwal P, Zhang B, Ho Y, Cook A, Li L, Mikhail FM, Wang Y, McLaughlin ME, Bhatia R.

Blood. 2017 Feb 23;129(8):1008-1020. doi: 10.1182/blood-2016-05-714089. Epub 2016 Dec 23.

10.

Buzz Juice: Neurological sequelae of synthetic cannabinoids.

Kak M, Mikhail F, Yano ST, Guan R, Lukas RV.

J Clin Neurosci. 2017 Mar;37:43. doi: 10.1016/j.jocn.2016.10.046. Epub 2016 Nov 16.

PMID:
27865819
11.

Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.

Hollenbeck D, Williams CL, Drazba K, Descartes M, Korf BR, Rutledge SL, Lose EJ, Robin NH, Carroll AJ, Mikhail FM.

Genet Med. 2017 Apr;19(4):377-385. doi: 10.1038/gim.2016.132. Epub 2016 Sep 15.

PMID:
27632688
12.

Section E6.5-6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor-acquired chromosomal abnormalities.

Cooley LD, Morton CC, Sanger WG, Saxe DF, Mikhail FM.

Genet Med. 2016 Jun;18(6):643-8. doi: 10.1038/gim.2016.51. Epub 2016 Apr 28.

PMID:
27124786
13.

Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalities.

Mikhail FM, Heerema NA, Rao KW, Burnside RD, Cherry AM, Cooley LD.

Genet Med. 2016 Jun;18(6):635-42. doi: 10.1038/gim.2016.50. Epub 2016 Apr 28. Erratum in: Genet Med. 2016 Aug;18(8):859.

PMID:
27124785
14.

Family history of hematologic malignancies and risk of multiple myeloma: differences by race and clinical features.

VanValkenburg ME, Pruitt GI, Brill IK, Costa L, Ehtsham M, Justement IT, Innis-Shelton RD, Salzman D, Reddy ES, Godby KN, Mikhail FM, Carroll AJ, Reddy VB, Sanderson RD, Justement LB, Sanders PW, Brown EE.

Cancer Causes Control. 2016 Jan;27(1):81-91. doi: 10.1007/s10552-015-0685-2. Epub 2015 Nov 23.

15.

Cleft palate in a patient with the nested 22q11.2 LCR C to D deletion.

Williams CL, Nelson KR, Grant JH, Mikhail FM, Robin NH.

Am J Med Genet A. 2016 Jan;170A(1):260-2. doi: 10.1002/ajmg.a.37408. Epub 2015 Sep 30. No abstract available.

PMID:
26419407
16.

Partial trisomy 21: a fifty-year follow-up visit.

Hamm JA, Carroll AJ, Mikhail FM, Korf BR, Finley WH.

Am J Med Genet A. 2015 Jul;167(7):1610-3. doi: 10.1002/ajmg.a.37031. Epub 2015 May 5.

PMID:
25944586
17.

Lack of exacerbation of neurodegeneration in a double transgenic mouse model of mutant LRRK2 and tau.

Mikhail F, Calingasan N, Parolari L, Subramanian A, Yang L, Flint Beal M.

Hum Mol Genet. 2015 Jun 15;24(12):3545-56. doi: 10.1093/hmg/ddv105. Epub 2015 Mar 24.

PMID:
25804954
18.

Sex-discordant monochorionic twins with blood and tissue chimerism.

Rodriguez-Buritica D, Rojnueangnit K, Messiaen LM, Mikhail FM, Robin NH.

Am J Med Genet A. 2015 Apr;167A(4):872-7. doi: 10.1002/ajmg.a.37022. Epub 2015 Feb 23.

PMID:
25708669
19.

Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or Palate.

Rojnueangnit K, Mikhail FM, Cui X, Yu S, Robin NH.

Cleft Palate Craniofac J. 2015 Nov;52(6):724-31. doi: 10.1597/14-088. Epub 2014 Dec 9.

PMID:
25489768
20.

Array comparative genomic hybridisation testing in CHD.

Hightower HB, Robin NH, Mikhail FM, Ambalavanan N.

Cardiol Young. 2015 Aug;25(6):1155-72. doi: 10.1017/S1047951114001838. Epub 2014 Oct 8.

PMID:
25296170
21.

Identification of large NF1 duplications reciprocal to NAHR-mediated type-1 NF1 deletions.

Kehrer-Sawatzki H, Bengesser K, Callens T, Mikhail F, Fu C, Hillmer M, Walker ME, Saal HM, Lacassie Y, Cooper DN, Messiaen L.

Hum Mutat. 2014 Dec;35(12):1469-75. doi: 10.1002/humu.22692.

PMID:
25205021
22.

Incidental detection of cancer predisposition gene copy number variations by array comparative genomic hybridization.

Hamm JA, Mikhail FM, Hollenbeck D, Farmer M, Robin NH.

J Pediatr. 2014 Nov;165(5):1057-9.e1-4. doi: 10.1016/j.jpeds.2014.07.042. Epub 2014 Sep 4.

PMID:
25201531
23.

Copy number variations and human genetic disease.

Mikhail FM.

Curr Opin Pediatr. 2014 Dec;26(6):646-52. doi: 10.1097/MOP.0000000000000142. Review.

PMID:
25198053
24.

Quality assurance and quality control in clinical cytogenetics.

Mikhail FM, Watson MS.

Curr Protoc Hum Genet. 2014 Jul 14;82:8.2.1-10. doi: 10.1002/0471142905.hg0802s82.

PMID:
25042720
25.

Palindrome-mediated and replication-dependent pathogenic structural rearrangements within the NF1 gene.

Hsiao MC, Piotrowski A, Alexander J, Callens T, Fu C, Mikhail FM, Claes KB, Messiaen L.

Hum Mutat. 2014 Jul;35(7):891-8. doi: 10.1002/humu.22569. Epub 2014 May 21.

PMID:
24760680
26.

Neuregulin-1 overexpression and Trp53 haploinsufficiency cooperatively promote de novo malignant peripheral nerve sheath tumor pathogenesis.

Brosius SN, Turk AN, Byer SJ, Brossier NM, Kohli L, Whitmire A, Mikhail FM, Roth KA, Carroll SL.

Acta Neuropathol. 2014 Apr;127(4):573-91.

27.

The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization system.

Mikhail FM, Burnside RD, Rush B, Ibrahim J, Godshalk R, Rutledge SL, Robin NH, Descartes MD, Carroll AJ.

Genet Med. 2014 Jan;16(1):92-100. doi: 10.1038/gim.2013.79. Epub 2013 Jun 13.

PMID:
23765049
28.

Inflammatory Flt3l is essential to mobilize dendritic cells and for T cell responses during Plasmodium infection.

Guermonprez P, Helft J, Claser C, Deroubaix S, Karanje H, Gazumyan A, Darasse-Jèze G, Telerman SB, Breton G, Schreiber HA, Frias-Staheli N, Billerbeck E, Dorner M, Rice CM, Ploss A, Klein F, Swiecki M, Colonna M, Kamphorst AO, Meredith M, Niec R, Takacs C, Mikhail F, Hari A, Bosque D, Eisenreich T, Merad M, Shi Y, Ginhoux F, Rénia L, Urban BC, Nussenzweig MC.

Nat Med. 2013 Jun;19(6):730-8. doi: 10.1038/nm.3197. Epub 2013 May 19.

29.

Transgenic mice overexpressing neuregulin-1 model neurofibroma-malignant peripheral nerve sheath tumor progression and implicate specific chromosomal copy number variations in tumorigenesis.

Kazmi SJ, Byer SJ, Eckert JM, Turk AN, Huijbregts RP, Brossier NM, Grizzle WE, Mikhail FM, Roth KA, Carroll SL.

Am J Pathol. 2013 Mar;182(3):646-67. doi: 10.1016/j.ajpath.2012.11.017. Epub 2013 Jan 13.

30.

Endoscopic ultrasound and endobronchial ultrasound-guided fine-needle aspiration of deep-seated lymphadenopathy: Analysis of 1338 cases.

Nunez AL, Jhala NC, Carroll AJ, Mikhail FM, Reddy VV, Xian RR, Jhala DN.

Cytojournal. 2012;9:14. doi: 10.4103/1742-6413.95845. Epub 2012 May 5.

31.

In vivo regulation of the heme oxygenase-1 gene in humanized transgenic mice.

Kim J, Zarjou A, Traylor AM, Bolisetty S, Jaimes EA, Hull TD, George JF, Mikhail FM, Agarwal A.

Kidney Int. 2012 Aug;82(3):278-91. doi: 10.1038/ki.2012.102. Epub 2012 Apr 11.

32.

Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders.

Mikhail FM, Lose EJ, Robin NH, Descartes MD, Rutledge KD, Rutledge SL, Korf BR, Carroll AJ.

Am J Med Genet A. 2011 Oct;155A(10):2386-96. doi: 10.1002/ajmg.a.34177.

PMID:
22031302
33.

Monosomy1p36.3 and trisomy 19p13.3 in a child with periventricular nodular heterotopia.

Descartes M, Mikhail FM, Franklin JC, McGrath TM, Bebin M.

Pediatr Neurol. 2011 Oct;45(4):274-8. doi: 10.1016/j.pediatrneurol.2011.06.002.

PMID:
21907895
34.

A case of acute promyelocytic leukemia without RARα rearrangement and apparently normal cytogenetics.

Vaklavas C, Steciuk MR, Ren Y, Baird MF, Mikhail FM, Foran JM.

Clin Lymphoma Myeloma Leuk. 2011 Dec;11(6):521-4. doi: 10.1016/j.clml.2011.03.036. Epub 2011 May 19. No abstract available.

PMID:
21729689
35.

Identification of SPRED1 deletions using RT-PCR, multiplex ligation-dependent probe amplification and quantitative PCR.

Spencer E, Davis J, Mikhail F, Fu C, Vijzelaar R, Zackai EH, Feret H, Meyn MS, Shugar A, Bellus G, Kocsis K, Kivirikko S, Pöyhönen M, Messiaen L.

Am J Med Genet A. 2011 Jun;155A(6):1352-9. doi: 10.1002/ajmg.a.33894. Epub 2011 May 5.

PMID:
21548021
36.

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.

Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, Potluri VR, Risheg H, Rush B, Smith JL, Schwartz S, Tepperberg JH, Butler MG.

Hum Genet. 2011 Oct;130(4):517-28. doi: 10.1007/s00439-011-0970-4. Epub 2011 Feb 27.

PMID:
21359847
37.

Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1).

Messiaen L, Vogt J, Bengesser K, Fu C, Mikhail F, Serra E, Garcia-Linares C, Cooper DN, Lazaro C, Kehrer-Sawatzki H.

Hum Mutat. 2011 Feb;32(2):213-9. doi: 10.1002/humu.21418.

PMID:
21280148
38.

Use of array comparative genome hybridization in orofacial clefting.

Gallego CJ, Grant J, Mikhail FM, Barger C, Robin NH.

J Craniofac Surg. 2010 Sep;21(5):1591-4. doi: 10.1097/SCS.0b013e3181ebcc9c.

PMID:
20856054
39.

Identification of PKHD1 multiexon deletions using multiplex ligation-dependent probe amplification and quantitative polymerase chain reaction.

Zvereff V, Yao S, Ramsey J, Mikhail FM, Vijzelaar R, Messiaen L.

Genet Test Mol Biomarkers. 2010 Aug;14(4):505-10. doi: 10.1089/gtmb.2009.0188.

PMID:
20575693
40.

Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia.

Harvey RC, Mullighan CG, Chen IM, Wharton W, Mikhail FM, Carroll AJ, Kang H, Liu W, Dobbin KK, Smith MA, Carroll WL, Devidas M, Bowman WP, Camitta BM, Reaman GH, Hunger SP, Downing JR, Willman CL.

Blood. 2010 Jul 1;115(26):5312-21. doi: 10.1182/blood-2009-09-245944. Epub 2010 Feb 4.

41.

Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia.

Mullighan CG, Collins-Underwood JR, Phillips LA, Loudin MG, Liu W, Zhang J, Ma J, Coustan-Smith E, Harvey RC, Willman CL, Mikhail FM, Meyer J, Carroll AJ, Williams RT, Cheng J, Heerema NA, Basso G, Pession A, Pui CH, Raimondi SC, Hunger SP, Downing JR, Carroll WL, Rabin KR.

Nat Genet. 2009 Nov;41(11):1243-6. doi: 10.1038/ng.469. Epub 2009 Oct 18.

42.

Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication.

Burnside RD, Lose EJ, Domínguez MG, Sánchez-Corona J, Rivera H, Carroll AJ, Mikhail FM.

Am J Med Genet A. 2009 Jul;149A(7):1516-22. doi: 10.1002/ajmg.a.32906.

PMID:
19533774
43.

A new syndrome with Stargardt macular degeneration, abnormalities of the corpus callosum, mental retardation, and dysmorphic features: a case report of two siblings.

Descartes M, Royal SA, Franklin J, Goodin K, Mancuso M, Mikhail FM, Holt L.

Clin Dysmorphol. 2009 Jul;18(3):178-80. doi: 10.1097/MCD.0b013e32832a9ef2. No abstract available.

PMID:
19451813
44.

Distal 22q11.2 microduplication encompassing the BCR gene.

Descartes M, Franklin J, Diaz de Ståhl T, Piotrowski A, Bruder CE, Dumanski JP, Carroll AJ, Mikhail FM.

Am J Med Genet A. 2008 Dec 1;146A(23):3075-81. doi: 10.1002/ajmg.a.32572.

PMID:
19006218
45.

Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities.

Descartes M, Hain JZ, Conklin M, Franklin J, Mikhail FM, Lachman RS, Nolet S, Messiaen LM.

Am J Med Genet A. 2008 Nov 15;146A(22):2937-43. doi: 10.1002/ajmg.a.32550.

PMID:
18925675
46.

A prenatally ascertained X;Y translocation characterized using conventional and molecular cytogenetics.

Burnside RD, Mikhail FM, Cosper PC.

Am J Med Genet A. 2008 May 1;146A(9):1221-4. doi: 10.1002/ajmg.a.32265. No abstract available.

PMID:
18384143
47.

A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.

Mikhail FM, Descartes M, Piotrowski A, Andersson R, Diaz de Ståhl T, Komorowski J, Bruder CE, Dumanski JP, Carroll AJ.

Am J Med Genet A. 2007 Sep 15;143A(18):2178-84.

PMID:
17676630
48.

Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).

Mikhail FM, Sathienkijkanchai A, Robin NH, Prucka S, Biggerstaff JS, Komorowski J, Andersson R, Bruder CE, Piotrowski A, Diaz de Ståhl T, Dumanski JP, Carroll AJ.

Am J Med Genet A. 2007 Aug 1;143A(15):1760-6.

PMID:
17603794
49.

Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2).

Mikhail FM, McIlvried D, Holt RL, Messiaen L, Descartes MD, Carroll AJ.

Am J Med Genet A. 2006 Aug 1;140(15):1647-54.

PMID:
16835929
50.

Normal and transforming functions of RUNX1: a perspective.

Mikhail FM, Sinha KK, Saunthararajah Y, Nucifora G.

J Cell Physiol. 2006 Jun;207(3):582-93. Review.

PMID:
16250015

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