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Books
Το αίνιγμα της κερασόπιτας / Βάσια Ακαρέπη
To ainigma tēs kerasopitas / Vasia Akarepē.
Author / Creator:Akarepē, Vasia, author. | Ακαρέπη, Βάσια, author
Publisher:Athēna : Dioptra, 2017
Call Numbers:GRE/010174
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Οι κερασιές θ' ανθίσουν και φέτος... μυθιστόρημα / Μενέλαος Λουντέμης.
Hoi kerasies th' anthisoun kai phetos... mythistorēma / Melelaos Lountemēs.
Author / Creator:Lountemēs, Menelaos, 1912-1977, author. | Λουντέμης, Μενέλαος, 1912-1977, author
Publisher:Athēna : Ekdoseis Patakē, 2015.
Call Numbers:GRE/01007
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ArticlesPeer ReviewedFull Text
Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and th...
Author / Creator:Riggs, Erin Rooney ; Andersen, Erica F. ; Cherry, Athena M. ; Kantarci, Sibel ; Kearney, Hutton ; Patel, Ankita ; Raca, Gordana ; Ritter, Deborah I. ; South, Sarah T. ; Thorland, Erik C. ; Pineda-Alvarez, Daniel ; Aradhya, Swaroop ; Martin, Christa Lese
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2020-02, Vol.22 (2), p.245-257
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ArticlesPeer ReviewedFull Text
Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells
Author / Creator:Sun, Ning ; Panetta, Nicholas J ; Gupta, Deepak M ; Wilson, Kitchener D ; Lee, Andrew ; Jia, Fangjun ; Hu, Shijun ; Cherry, Athena M ; Robbins, Robert C ; Longaker, Michael T ; Wu, Joseph C
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2009-09, Vol.106 (37), p.15720-15725
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ArticlesPeer ReviewedFull Text
Loss of SMARCB1/INI1 expression in poorly differentiated chordomas
Author / Creator:Mobley, Bret C. ; McKenney, Jesse K. ; Bangs, Charles D. ; Callahan, Katherine ; Yeom, Kristen W. ; Schneppenheim, Reinhard ; Hayden, Melanie G. ; Cherry, Athena M. ; Gokden, Murat ; Edwards, Michael S. B. ; Fisher, Paul G. ; Vogel, Hannes
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Acta neuropathologica, 2010-12, Vol.120 (6), p.745-753
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ArticlesPeer ReviewedFull Text
CTCF Mediates Interchromosomal Colocalization between Igf2/H19 and Wsb1/Nf1
Author / Creator:Ling, Jian Qun ; Li, Tao ; Hu, Ji Fan ; Vu, Thanh H. ; Chen, Hui Ling ; Qiu, Xin Wen ; Cherry, Athena M. ; Hoffman, Andrew R.
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2006-04, Vol.312 (5771), p.269-272
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ArticlesPeer ReviewedFull Text
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG)
Author / Creator:Cherry, Athena M ; Akkari, Yassmine M ; Barr, Kimberly M ; Kearney, Hutton M ; Rose, Nancy C ; South, Sarah T ; Tepperberg, James H ; Meck, Jeanne M
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2017-08, Vol.19 (8), p.845-850
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ArticlesPeer ReviewedFull Text
Section E6.1–6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow–acquired chromosomal abnormalities
Author / Creator:Mikhail, Fady M. ; Heerema, Nyla A. ; Rao, Kathleen W. ; Burnside, Rachel D. ; Cherry, Athena M. ; Cooley, Linda D.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2016-06, Vol.18 (6), p.635-642
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ArticlesPeer ReviewedFull Text
Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (...
Author / Creator:Riggs, Erin Rooney ; Andersen, Erica F. ; Cherry, Athena M. ; Kantarci, Sibel ; Kearney, Hutton ; Patel, Ankita ; Raca, Gordana ; Ritter, Deborah I. ; South, Sarah T. ; Thorland, Erik C. ; Pineda-Alvarez, Daniel ; Aradhya, Swaroop ; Martin, Christa Lese
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2021-11, Vol.23 (11), p.2230-2230
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ArticlesPeer ReviewedFull Text
Hidden mastocytosis in acute myeloid leukemia with t(8;21)(q22;q22)
Author / Creator:Johnson, Ryan C ; Savage, Natasha M ; Chiang, Tsoyu ; Gotlib, Jason R ; Cherry, Athena M ; Arber, Daniel A ; George, Tracy I
Publisher:England: Oxford University Press
Journal title:American journal of clinical pathology, 2013-10, Vol.140 (4), p.525-535
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ArticlesPeer ReviewedFull Text
Characterization of D-cyclin proteins in hematolymphoid neoplasms: lack of specificity of cyclin-D2 and D3 expression in lymphoma subtypes
Author / Creator:Metcalf, Ryan A ; Zhao, Shuchun ; Anderson, Matthew W ; Lu, Zhi Shun ; Galperin, Ilana ; Marinelli, Robert J ; Cherry, Athena M ; Lossos, Izidore S ; Natkunam, Yasodha
Publisher:New York: Nature Publishing Group US
Journal title:Modern pathology, 2010-03, Vol.23 (3), p.420-433
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ArticlesPeer ReviewedFull Text
Cytogenetic Variation of B-Lymphoblastic Leukemia With Intrachromosomal Amplification of Chromosome 21 (iAMP21): A Multi-Institutional Series Review
Author / Creator:Johnson, Ryan C ; Weinberg, Olga K ; Cascio, Michael J ; Dahl, Gary V ; Mitton, Bryan A ; Silverman, Lewis B ; Cherry, Athena M ; Arber, Daniel A ; Ohgami, Robert S
Publisher:England: Oxford University Press
Journal title:American journal of clinical pathology, 2015-07, Vol.144 (1), p.103-112
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ArticlesPeer ReviewedFull Text
Isolated Follicles Enriched for Centroblasts and Lacking t(14;18)/BCL2 in Lymphoid Tissue: Diagnostic and Clinical Implications
Author / Creator:Nybakken, Grant E ; Bala, Rajeev ; Gratzinger, Dita ; Jones, Carol D ; Zehnder, James L ; Bangs, Charles D ; Cherry, Athena ; Warnke, Roger A ; Natkunam, Yasodha
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-03, Vol.11 (3), p.e0151735
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ArticlesPeer ReviewedFull Text
B-cell transcription factor expression and immunoglobulin gene rearrangement frequency in acute myeloid leukemia with t(8;21)(q22;q22)
Author / Creator:Johnson, Ryan C ; Ma, Lisa ; Cherry, Athena M ; Arber, Daniel A ; George, Tracy I
Publisher:England: Oxford University Press
Journal title:American journal of clinical pathology, 2013-09, Vol.140 (3), p.355-362
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Terminal 22q deletion syndrome: A newly recognized cause of speech and language disability in the autism spectrum
Author / Creator:MANNING, Melanie A ; CASSIDY, Suzanne B ; CLERICUZIO, Carol ; CHERRY, Athena M ; SCHWARTZ, Stuart ; HUDGINS, Louanne ; ENNS, Gregory M ; HOYME, H. Eugene
Publisher:Elk Grove Village, IL: American Academy of Pediatrics
Journal title:Pediatrics (Evanston), 2004-08, Vol.114 (2), p.451-457
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Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics
Author / Creator:Bieber, Frederick R. ; Cherry, Athena M. ; Emanuel, Beverly S. ; Francke, Uta ; Hoyme, H. Eugene ; Jackson, Laird G. ; Morton, Cynthia C. ; Muenke, Maximillian ; Powell, Cynthia M. ; Punnett, Hope H. ; Rao, P. Nagesh ; Schwartz, Stuart ; Stevenson, Roger E. ; Van Dyke, Daniel L.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2017-03, Vol.19 (3), p.294-296
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Defective Double-Strand DNA Break Repair and Chromosomal Translocations by MYC Overexpression
Author / Creator:Karlsson, Asa ; Deb-Basu, Debabrita ; Cherry, Athena ; Turner, Stephanie ; Ford, James ; Felsher, Dean W.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2003-08, Vol.100 (17), p.9974-9979
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Risk categorization for oversight of laboratory-developed tests for inherited conditions
Author / Creator:Monaghan, Kristin G. ; Benkendorf, Judith ; Cherry, Athena M. ; Gross, Susan J. ; Richards, C. Sue ; Sutton, Vernon Reid ; Watson, Michael S.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2013-04, Vol.15 (4), p.314-315
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Gliosarcoma with melanocytic differentiation
Author / Creator:Dulai, Mohanpal S. ; Moes, Gregory S. ; Briley, Anita L. ; Galperin, Ilana B. ; Smyth, Lawrence ; Cherry, Athena M. ; Lehman, Norman L.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Acta neuropathologica, 2008-03, Vol.115 (3), p.357-361
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ArticlesPeer ReviewedFull Text
Complete remission of primary plasma cell leukemia with bortezomib, doxorubicin, and dexamethasone: a case report
Author / Creator:Chan, Steven M ; George, Tracy ; Cherry, Athena M ; Medeiros, Bruno C
Publisher:England: Cases Network Ltd
Journal title:Cases journal, 2009-02, Vol.2 (1), p.121-121, Article 121
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To ainigma tēs kerasopitas / Vasia Akarepē.

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Hoi kerasies th' anthisoun kai phetos... mythistorēma / Melelaos Lountemēs.

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Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and th...

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Feeder-free derivation of induced pluripotent stem cells from adult human adipose stem cells

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Loss of SMARCB1/INI1 expression in poorly differentiated chordomas

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CTCF Mediates Interchromosomal Colocalization between Igf2/H19 and Wsb1/Nf1

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Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG)

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

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Correction: Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (...

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Hidden mastocytosis in acute myeloid leukemia with t(8;21)(q22;q22)

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Characterization of D-cyclin proteins in hematolymphoid neoplasms: lack of specificity of cyclin-D2 and D3 expression in lymphoma subtypes

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Cytogenetic Variation of B-Lymphoblastic Leukemia With Intrachromosomal Amplification of Chromosome 21 (iAMP21): A Multi-Institutional Series Review

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Isolated Follicles Enriched for Centroblasts and Lacking t(14;18)/BCL2 in Lymphoid Tissue: Diagnostic and Clinical Implications

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B-cell transcription factor expression and immunoglobulin gene rearrangement frequency in acute myeloid leukemia with t(8;21)(q22;q22)

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Terminal 22q deletion syndrome: A newly recognized cause of speech and language disability in the autism spectrum

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Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics

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Defective Double-Strand DNA Break Repair and Chromosomal Translocations by MYC Overexpression

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Risk categorization for oversight of laboratory-developed tests for inherited conditions

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Gliosarcoma with melanocytic differentiation

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Complete remission of primary plasma cell leukemia with bortezomib, doxorubicin, and dexamethasone: a case report

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