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Detection of Early Alzheimer's disease at AdventHealth: A Davos Alzheimer's Collaborative flagship site.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.083046
By:
- Baldivieso, Valeria;
- Erickson, Kirk I.;
- Smith, Steven R.;
- Pratley, Richard E.;
- Baksh, Magda R.;
- Shepherd, Gayle;
- Lopez, Janice;
- Jain, Shivangi;
- Selzler, Katherine J.;
- Murray, James F;
- West, Tim;
- Ortega, Julia;
- Coppinger, Justine;
- Venkatesh, Venky;
- Monane, Mark;
- Braunstein, Joel B.
Publication type:
Article
Framework for disclosing AD biomarker results following cognitive assessment within a pragmatic, multi‐country implementation evaluation.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 7, p. 1, doi. 10.1002/alz.063746
By:
- MacLeod, Tim;
- Baksh, Magda Ruth;
- Filho, Otelo Corrêa dos Santos;
- Govia, Ishtar;
- Robledo, Luis Miguel Gutierrez;
- Kowa, Hisatomo;
- Ritchie, Craig W.;
- Willis, Deanna R;
- Coppinger, Justine;
- Ball, Daniel E;
- Murray, James F;
- Largent, Emily A.
Publication type:
Article
The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective.
Published in:
Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00244
By:
- Latham, Gary J.;
- Coppinger, Justine;
- Hadd, Andrew G.;
- Nolin, Sarah L.
Publication type:
Article
Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications.
Published in:
Journal of Neurodevelopmental Disorders, 2010, v. 2, n. 1, p. 26, doi. 10.1007/s11689-009-9037-4
By:
- Rosenfeld, Jill;
- Coppinger, Justine;
- Bejjani, Bassem;
- Girirajan, Santhosh;
- Eichler, Evan;
- Shaffer, Lisa;
- Ballif, Blake
Publication type:
Article
Deletions flanked by breakpoints 3 and 4 on 15q13 may contribute to abnormal phenotypes.
Published in:
European Journal of Human Genetics, 2011, v. 19, n. 5, p. 547, doi. 10.1038/ejhg.2010.237
By:
- Rosenfeld, Jill A.;
- Stephens, Lindsey E.;
- Coppinger, Justine;
- Ballif, Blake C;
- Hoo, Joe J.;
- French, Beatrice N.;
- Banks, Valerie C.;
- Smith, Wendy E.;
- Manchester, David;
- Tsai, Anne Chun-Hui;
- Merrion, Katrina;
- Mendoza-Londono, Roberto;
- Dupuis, Lucie;
- Schultz, Roger;
- Torchia, Beth;
- Sahoo, Trilochan;
- Bejjani, Bassem;
- Weaver, David D.;
- Shaffer, Lisa G.
Publication type:
Article
Altered Distribution of Mitochondria and Actin Fibers in 3T3 Cells Cultured on Microcarriers.
Published in:
Biotechnology Progress, 1992, v. 8, n. 6, p. 572, doi. 10.1021/bp00018a600
By:
- Laney, Tracey V.Du;
- Cherry, Robert S.;
- Coppinger, Justine A.;
- Truskey, George A.
Publication type:
Article
A blood biomarker test for brain amyloid impacts the clinical evaluation of cognitive impairment.
Published in:
Annals of Clinical & Translational Neurology, 2023, v. 10, n. 10, p. 1738, doi. 10.1002/acn3.51863
By:
- Monane, Mark;
- Johnson, Kim G.;
- Snider, B. Joy;
- Turner, Raymond S.;
- Drake, Jonathan D.;
- Maraganore, Demetrius M.;
- Bicksel, James L.;
- Jacobs, Daniel H.;
- Ortega, Julia L.;
- Henderson, Joni;
- Jiang, Yan;
- Huang, Shuguang;
- Coppinger, Justine;
- Fogelman, Ilana;
- West, Tim;
- Braunstein, Joel B.
Publication type:
Article
Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Published in:
Prenatal Diagnosis, 2012, v. 32, n. 10, p. 976, doi. 10.1002/pd.3945
By:
- Shaffer, Lisa G.;
- Dabell, Mindy P.;
- Fisher, Allan J.;
- Coppinger, Justine;
- Bandholz, Anne M.;
- Ellison, Jay W.;
- Ravnan, J. Britt;
- Torchia, Beth S.;
- Ballif, Blake C.;
- Rosenfeld, Jill A.
Publication type:
Article
Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Published in:
Prenatal Diagnosis, 2012, v. 32, n. 10, p. 986, doi. 10.1002/pd.3943
By:
- Shaffer, Lisa G;
- Rosenfeld, Jill A;
- Dabell, Mindy P;
- Coppinger, Justine;
- Bandholz, Anne M;
- Ellison, Jay W;
- Ravnan, J Britt;
- Torchia, Beth S;
- Ballif, Blake C;
- Fisher, Allan J
Publication type:
Article
Referral patterns for microarray testing in prenatal diagnosis.
Published in:
Prenatal Diagnosis, 2012, v. 32, n. 6, p. 611, doi. 10.1002/pd.3909
By:
- Shaffer, Lisa G.;
- Dabell, Mindy Preston;
- Rosenfeld, Jill A.;
- Neill, Nicholas J.;
- Ballif, Blake C.;
- Coppinger, Justine;
- Diwan, Noa Rinzler;
- Chong, Karen;
- Shohat, Mordechai;
- Chitayat, David
Publication type:
Article
Referral patterns for microarray testing in prenatal diagnosis.
Published in:
Prenatal Diagnosis, 2012, v. 32, n. 4, p. 344, doi. 10.1002/pd.3856
By:
- Shaffer, Lisa G.;
- Dabell, Mindy Preston;
- Rosenfeld, Jill A.;
- Neill, Nicholas J.;
- Ballif, Blake C.;
- Coppinger, Justine;
- Diwan, Noa Rinzler;
- Chong, Karen;
- Shohat, Mordechai;
- Chitayat, David
Publication type:
Article
The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.
Published in:
Prenatal Diagnosis, 2011, v. 31, n. 8, p. 778, doi. 10.1002/pd.2766
By:
- Shaffer, Lisa G.;
- Coppinger, Justine;
- Morton, S. Annie;
- Alliman, Sarah;
- Burleson, Jessica;
- Traylor, Ryan;
- Walker, Cathryn;
- Byerly, Steve;
- Lamb, Allen N.;
- Schultz, Roger;
- Ravnan, J. Britt;
- Kashork, Catherine D.;
- Torchia, Beth S.;
- Sulpizio, Scott;
- Sundin, Kyle;
- Schermer, Mack;
- Adler, Karl;
- Dallaire, Stephanie;
- Ballif, Blake C.
Publication type:
Article
Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.
Published in:
Prenatal Diagnosis, 2010, v. 30, n. 12/13, p. 1131, doi. 10.1002/pd.2626
By:
- Maya, Idit;
- Davidov, Bella;
- Gershovitz, Liron;
- Zalzstein, Yael;
- Taub, Ellen;
- Coppinger, Justine;
- Shaffer, Lisa G.;
- Shohat, Mordechai
Publication type:
Article
Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray.
Published in:
Prenatal Diagnosis, 2009, v. 29, n. 12, p. 1156, doi. 10.1002/pd.2371
By:
- Coppinger, Justine;
- Alliman, Sarah;
- Lamb, Allen N.;
- Torchia, Beth S.;
- Bejjani, Bassem A.;
- Shaffer, Lisa G.
Publication type:
Article
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
Published in:
Prenatal Diagnosis, 2008, v. 28, n. 9, p. 789, doi. 10.1002/pd.2053
By:
- Shaffer, Lisa G.;
- Coppinger, Justine;
- Alliman, Sarah;
- Torchia, Beth A.;
- Theisen, Aaron;
- Ballif, Blake C.;
- Bejjani, Bassem A.
Publication type:
Article
Identification of familial and de novo microduplications of 22q11.21–q11.23 distal to the 22q11.21 microdeletion syndrome region.
Published in:
Human Molecular Genetics, 2009, v. 18, n. 8, p. 1377, doi. 10.1093/hmg/ddp042
By:
- Coppinger, Justine;
- McDonald-McGinn, Donna;
- Zackai, Elaine;
- Shane, Kate;
- Atkin, Joan F.;
- Asamoah, Alexander;
- Leland, Robert;
- Weaver, David D.;
- Lansky-Shafer, Susan;
- Schmidt, Karen;
- Feldman, Heidi;
- Cohen, William;
- Phalin, Judy;
- Powell, Berkley;
- Ballif, Blake C.;
- Theisen, Aaron;
- Geiger, Elizabeth;
- Haldeman-Englert, Chad;
- Shaikh, Tamim H.;
- Saitta, Sulagna
Publication type:
Article

Found: 16