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Items: 38

1.

Effect of endomyocardial biopsy on levels of donor-specific cell-free DNA.

Zangwill SD, Stamm KD, Hidestrand M, Tomita-Mitchell A, Mitchell ME.

J Heart Lung Transplant. 2019 Oct;38(10):1118-1120. doi: 10.1016/j.healun.2019.06.005. Epub 2019 Jun 28. No abstract available.

PMID:
31324442
2.

Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta.

LaDisa JF Jr, Tomita-Mitchell A, Stamm K, Bazan K, Mahnke DK, Goetsch MA, Wegter BJ, Gerringer JW, Repp K, Palygin O, Zietara AP, Krolikowski MM, Eddinger TJ, Alli AA, Mitchell ME.

Physiol Genomics. 2019 Jun 1;51(6):177-185. doi: 10.1152/physiolgenomics.00049.2018. Epub 2019 Apr 19.

PMID:
31002586
3.

GSEPD: a Bioconductor package for RNA-seq gene set enrichment and projection display.

Stamm K, Tomita-Mitchell A, Bozdag S.

BMC Bioinformatics. 2019 Mar 6;20(1):115. doi: 10.1186/s12859-019-2697-5.

4.

Metakaryotic cells linked to pediatric pulmonary vein stenosis.

Kirkpatrick EC, Mitchell ME, Thilly WG, Hidestrand P, Tomita-Mitchell A, Hidestrand M, Gostjeva EV.

Cardiovasc Pathol. 2019 Mar - Apr;39:51-53. doi: 10.1016/j.carpath.2018.12.005. Epub 2018 Dec 21. No abstract available.

PMID:
30660022
5.

Noninvasive Assay for Donor Fraction of Cell-Free DNA in Pediatric Heart Transplant Recipients.

Ragalie WS, Stamm K, Mahnke D, Liang HL, Simpson P, Katz R, Tomita-Mitchell A, Kindel SJ, Zangwill S, Mitchell ME.

J Am Coll Cardiol. 2018 Jun 26;71(25):2982-2983. doi: 10.1016/j.jacc.2018.04.026. No abstract available.

6.

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.

Guo T, Repetto GM, McDonald McGinn DM, Chung JH, Nomaru H, Campbell CL, Blonska A, Bassett AS, Chow EWC, Mlynarski EE, Swillen A, Vermeesch J, Devriendt K, Gothelf D, Carmel M, Michaelovsky E, Schneider M, Eliez S, Antonarakis SE, Coleman K, Tomita-Mitchell A, Mitchell ME, Digilio MC, Dallapiccola B, Marino B, Philip N, Busa T, Kushan-Wells L, Bearden CE, Piotrowicz M, Hawuła W, Roberts AE, Tassone F, Simon TJ, van Duin EDA, van Amelsvoort TA, Kates WR, Zackai E, Johnston HR, Cutler DJ, Agopian AJ, Goldmuntz E, Mitchell LE, Wang T, Emanuel BS, Morrow BE; International 22q11.2 Consortium/Brain and Behavior Consortium*.

Circ Cardiovasc Genet. 2017 Oct;10(5). pii: e001690. doi: 10.1161/CIRCGENETICS.116.001690.

7.

Impact of MYH6 variants in hypoplastic left heart syndrome.

Tomita-Mitchell A, Stamm KD, Mahnke DK, Kim MS, Hidestrand PM, Liang HL, Goetsch MA, Hidestrand M, Simpson P, Pelech AN, Tweddell JS, Benson DW, Lough JW, Mitchell ME.

Physiol Genomics. 2016 Dec 1;48(12):912-921. doi: 10.1152/physiolgenomics.00091.2016. Epub 2016 Oct 27.

8.

Ciliopathy variant burden and developmental delay in children with hypoplastic left heart syndrome.

Geddes GC, Stamm K, Mitchell M, Mussatto KA, Tomita-Mitchell A.

Genet Med. 2017 Jun;19(6):711-714. doi: 10.1038/gim.2016.167. Epub 2016 Oct 27.

PMID:
27787502
9.

Effect of 22q11.2 deletion on bleeding and transfusion utilization in children with congenital heart disease undergoing cardiac surgery.

Brenner MK, Clarke S, Mahnke DK, Simpson P, Bercovitz RS, Tomita-Mitchell A, Mitchell ME, Newman DK.

Pediatr Res. 2016 Feb;79(2):318-24. doi: 10.1038/pr.2015.216. Epub 2015 Oct 22.

10.

Activin-A and Bmp4 levels modulate cell type specification during CHIR-induced cardiomyogenesis.

Kim MS, Horst A, Blinka S, Stamm K, Mahnke D, Schuman J, Gundry R, Tomita-Mitchell A, Lough J.

PLoS One. 2015 Feb 23;10(2):e0118670. doi: 10.1371/journal.pone.0118670. eCollection 2015.

11.

Use of cell-free fetal DNA in maternal plasma for noninvasive prenatal screening.

Wagner AJ, Mitchell ME, Tomita-Mitchell A.

Clin Perinatol. 2014 Dec;41(4):957-66. doi: 10.1016/j.clp.2014.08.013. Epub 2014 Oct 1. Review.

PMID:
25459783
12.

The inferred cardiogenic gene regulatory network in the mammalian heart.

Bazil JN, Stamm KD, Li X, Thiagarajan R, Nelson TJ, Tomita-Mitchell A, Beard DA.

PLoS One. 2014 Jun 27;9(6):e100842. doi: 10.1371/journal.pone.0100842. eCollection 2014.

13.

Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.

Thorsson T, Russell WW, El-Kashlan N, Soemedi R, Levine J, Geisler SB, Ackley T, Tomita-Mitchell A, Rosenfeld JA, Töpf A, Tayeh M, Goodship J, Innis JW, Keavney B, Russell MW.

Congenit Heart Dis. 2015 May-Jun;10(3):193-208. doi: 10.1111/chd.12179. Epub 2014 Apr 11.

14.

Highly sensitive noninvasive cardiac transplant rejection monitoring using targeted quantification of donor-specific cell-free deoxyribonucleic acid.

Hidestrand M, Tomita-Mitchell A, Hidestrand PM, Oliphant A, Goetsch M, Stamm K, Liang HL, Castleberry C, Benson DW, Stendahl G, Simpson PM, Berger S, Tweddell JS, Zangwill S, Mitchell ME.

J Am Coll Cardiol. 2014 Apr 1;63(12):1224-1226. doi: 10.1016/j.jacc.2013.09.029. Epub 2013 Oct 16. No abstract available.

15.

Use of combination chemotherapy for treatment of granulomatous and lymphocytic interstitial lung disease (GLILD) in patients with common variable immunodeficiency (CVID).

Chase NM, Verbsky JW, Hintermeyer MK, Waukau JK, Tomita-Mitchell A, Casper JT, Singh S, Shahir KS, Tisol WB, Nugent ML, Rao RN, Mackinnon AC, Goodman LR, Simpson PM, Routes JM.

J Clin Immunol. 2013 Jan;33(1):30-9. doi: 10.1007/s10875-012-9755-3. Epub 2012 Aug 29.

16.

Human gene copy number spectra analysis in congenital heart malformations.

Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME.

Physiol Genomics. 2012 May 1;44(9):518-41. doi: 10.1152/physiolgenomics.00013.2012. Epub 2012 Feb 7.

17.

Influence of temperature during transportation on cell-free DNA analysis.

Hidestrand M, Stokowski R, Song K, Oliphant A, Deavers J, Goetsch M, Simpson P, Kuhlman R, Ames M, Mitchell M, Tomita-Mitchell A.

Fetal Diagn Ther. 2012;31(2):122-8. doi: 10.1159/000335020. Epub 2012 Jan 19.

PMID:
22261730
18.

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.

Sparks AB, Wang ET, Struble CA, Barrett W, Stokowski R, McBride C, Zahn J, Lee K, Shen N, Doshi J, Sun M, Garrison J, Sandler J, Hollemon D, Pattee P, Tomita-Mitchell A, Mitchell M, Stuelpnagel J, Song K, Oliphant A.

Prenat Diagn. 2012 Jan;32(1):3-9. doi: 10.1002/pd.2922. Epub 2012 Jan 6.

19.

Exploring the environmental and genetic etiologies of congenital heart defects: the Wisconsin Pediatric Cardiac Registry.

Harris SE, Cronk C, Cassidy LD, Simpson P, Tomita-Mitchell A, Pelech AN.

J Registry Manag. 2011 Spring;38(1):24-9.

PMID:
22097702
20.

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.

Worthey EA, Mayer AN, Syverson GD, Helbling D, Bonacci BB, Decker B, Serpe JM, Dasu T, Tschannen MR, Veith RL, Basehore MJ, Broeckel U, Tomita-Mitchell A, Arca MJ, Casper JT, Margolis DA, Bick DP, Hessner MJ, Routes JM, Verbsky JW, Jacob HJ, Dimmock DP.

Genet Med. 2011 Mar;13(3):255-62. doi: 10.1097/GIM.0b013e3182088158.

PMID:
21173700
21.

Non-invasive prenatal detection of trisomy 21 using tandem single nucleotide polymorphisms.

Ghanta S, Mitchell ME, Ames M, Hidestrand M, Simpson P, Goetsch M, Thilly WG, Struble CA, Tomita-Mitchell A.

PLoS One. 2010 Oct 8;5(10):e13184. doi: 10.1371/journal.pone.0013184.

22.

Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease.

Tomita-Mitchell A, Mahnke DK, Larson JM, Ghanta S, Feng Y, Simpson PM, Broeckel U, Duffy K, Tweddell JS, Grossman WJ, Routes JM, Mitchell ME.

Physiol Genomics. 2010 Sep;42A(1):52-60. doi: 10.1152/physiolgenomics.00073.2010. Epub 2010 Jun 15.

23.

Metakaryotic stem cell lineages in organogenesis of humans and other metazoans.

Gostjeva EV, Koledova V, Tomita-Mitchell A, Mitchell M, Goetsch MA, Varmuza S, Fomina JN, Darroudi F, Thilly WG.

Organogenesis. 2009 Oct;5(4):191-200.

24.

Investigation of somatic NKX2-5 mutations in congenital heart disease.

Draus JM Jr, Hauck MA, Goetsch M, Austin EH 3rd, Tomita-Mitchell A, Mitchell ME.

J Med Genet. 2009 Feb;46(2):115-22. doi: 10.1136/jmg.2008.060277.

25.

GATA4 sequence variants in patients with congenital heart disease.

Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E.

J Med Genet. 2007 Dec;44(12):779-83.

26.

The molecular basis of congenital heart disease.

Mitchell ME, Sander TL, Klinkner DB, Tomita-Mitchell A.

Semin Thorac Cardiovasc Surg. 2007 Fall;19(3):228-37. Review.

PMID:
17983950
27.

Spectrum of heart disease associated with murine and human GATA4 mutation.

Rajagopal SK, Ma Q, Obler D, Shen J, Manichaikul A, Tomita-Mitchell A, Boardman K, Briggs C, Garg V, Srivastava D, Goldmuntz E, Broman KW, Benson DW, Smoot LB, Pu WT.

J Mol Cell Cardiol. 2007 Dec;43(6):677-85. Epub 2007 Jun 21.

28.

Molecular and cellular basis of congenital heart disease.

Sander TL, Klinkner DB, Tomita-Mitchell A, Mitchell ME.

Pediatr Clin North Am. 2006 Oct;53(5):989-1009, x. Review. Erratum in: Pediatr Clin North Am. 2009 Aug;56(4):xix.

PMID:
17027620
29.

Design of an automated multicapillary instrument with fraction collection for DNA mutation discovery by constant denaturant capillary electrophoresis (CDCE).

Li Q, Deka C, Glassner BJ, Arnold K, Li-Sucholeiki XC, Tomita-Mitchell A, Thilly WG, Karger BL.

J Sep Sci. 2005 Aug;28(12):1375-89.

PMID:
16138690
30.

Scanning the beta-globin gene for mutations in large populations by denaturing capillary and gel electrophoresis.

Li-Sucholeiki XC, Hu G, Perls T, Tomita-Mitchell A, Thilly WG.

Electrophoresis. 2005 Jun;26(13):2531-8.

PMID:
15948210
31.

Detection and frequency estimation of rare variants in pools of genomic DNA from large populations using mutational spectrometry.

Li-Sucholeiki XC, Tomita-Mitchell A, Arnold K, Glassner BJ, Thompson T, Murthy JV, Berk L, Lange C, Leong-Morgenthaler PM, MacDougall D, Munro J, Cannon D, Mistry T, Miller A, Deka C, Karger B, Gillespie KM, Ekstrøm PO, Todd JA, Thilly WG.

Mutat Res. 2005 Mar 1;570(2):267-80.

PMID:
15708585
32.

Diversity and dynamics of a north atlantic coastal Vibrio community.

Thompson JR, Randa MA, Marcelino LA, Tomita-Mitchell A, Lim E, Polz MF.

Appl Environ Microbiol. 2004 Jul;70(7):4103-10.

33.

The mutational spectrum of the HPRT gene from human T cells in vivo shares a significant concordant set of hot spots with MNNG-treated human cells.

Tomita-Mitchell A, Ling LL, Glover CL, Goodluck-Griffith J, Thilly WG.

Cancer Res. 2003 Sep 15;63(18):5793-8.

34.

Identification of in vivo mutations in exon 5 of the human HPRT gene in a set of pooled T-cell mutants by constant denaturant capillary electrophoresis (CDCE).

Fält S, Kumar R, Wennborg A, Tomita-Mitchell A, Thilly WG, Lambert B.

Mutat Res. 2000 Jul 20;452(1):57-66.

PMID:
10894891
35.

Mismatch repair deficient human cells: spontaneous and MNNG-induced mutational spectra in the HPRT gene.

Tomita-Mitchell A, Kat AG, Marcelino LA, Li-Sucholeiki XC, Goodluck-Griffith J, Thilly WG.

Mutat Res. 2000 May 30;450(1-2):125-38.

PMID:
10838138
36.

Population risk and physiological rate parameters for colon cancer. The union of an explicit model for carcinogenesis with the public health records of the United States.

Herrero-Jimenez P, Tomita-Mitchell A, Furth EE, Morgenthaler S, Thilly WG.

Mutat Res. 2000 Jan 17;447(1):73-116.

PMID:
10686307
37.

Single nucleotide polymorphism spectra in newborns and centenarians: identification of genes coding for rise of mortal disease.

Tomita-Mitchell A, Muniappan BP, Herrero-Jimenez P, Zarbl H, Thilly WG.

Gene. 1998 Nov 26;223(1-2):381-91.

PMID:
9858772
38.

Mutation, cell kinetics, and subpopulations at risk for colon cancer in the United States.

Herrero-Jimenez P, Thilly G, Southam PJ, Tomita-Mitchell A, Morgenthaler S, Furth EE, Thilly WG.

Mutat Res. 1998 May 25;400(1-2):553-78.

PMID:
9685710

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