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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 the Clinical Genome Resource (ClinGen)

Genetics in medicine, 2020-02, Vol.22 (2), p.245-257

2020

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

Proceedings of the National Academy of Sciences - PNAS, 2009-09, Vol.106 (37), p.15720-15725

2009

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A Clinicopathologic and Molecular Analysis of 34 Mediastinal Germ Cell Tumors Suggesting Different Modes of Teratoma Development

The American journal of surgical pathology, 2018-12, Vol.42 (12), p.1662-1673

2018

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Is it time to sound an alarm about false-positive cell-free DNA testing for fetal aneuploidy?

American journal of obstetrics and gynecology, 2013-11, Vol.209 (5), p.415-419

2013

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Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings

American journal of obstetrics and gynecology, 2015-08, Vol.213 (2), p.214.e1-214.e5

2015

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Loss of SMARCB1/INI1 expression in poorly differentiated chordomas

Acta neuropathologica, 2010-12, Vol.120 (6), p.745-753

2010

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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 (ACMG) and the Clinical Genome Resource (ClinGen)

Genetics in medicine, 2021-11, Vol.23 (11), p.2230-2230

2021

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Still a screening test: more attention needed to noninvasive prenatal test false-positive rates

American journal of obstetrics and gynecology, 2013-08, Vol.209 (2), p.160-161

2013

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

Modern pathology, 2010-03, Vol.23 (3), p.420-433

2010

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Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes

Haematologica (Roma), 2013-11, Vol.98 (11), p.1689-1696

2013

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Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?

Leukemia research, 2012-07, Vol.36 (7), p.832-840

2012

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

Science (American Association for the Advancement of Science), 2006-04, Vol.312 (5771), p.269-272

2006

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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)

Genetics in medicine, 2017-08, Vol.19 (8), p.845-850

2017

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Overexpression of the Anaphase Promoting Complex/Cyclosome Inhibitor Emi1 Leads to Tetraploidy and Genomic Instability of p53-Deficient Cells

Cell cycle (Georgetown, Tex.), 2006-07, Vol.5 (14), p.1569-1573

2006

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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

Genetics in medicine, 2016-06, Vol.18 (6), p.635-642

2016

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HER2 expression in gastric and gastroesophageal junction adenocarcinoma in a US population: clinicopathologic analysis with proposed approach to HER2 assessment

Applied immunohistochemistry & molecular morphology, 2012-01, Vol.20 (1), p.13

2012

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Terminal deletion of 6p results in a recognizable phenotype

American journal of medical genetics. Part A, 2005-07, Vol.136A (2), p.162-168

2005

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Immune checkpoint blockade as a potential therapeutic strategy for undifferentiated malignancies

Human pathology, 2018-12, Vol.82, p.39-45

2018

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Acute leukemia in a patient with 15q overgrowth syndrome

American journal of medical genetics. Part A, 2019-06, Vol.179 (6), p.1025-1029

2019

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

American journal of clinical pathology, 2013-10, Vol.140 (4), p.525-535

2013

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Investigating human placentation and pregnancy using first trimester chorionic villi

Placenta (Eastbourne), 2018-05, Vol.65, p.65-75

2018

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Long-term remission of Philadelphia chromosome–positive acute lymphoblastic leukemia after allogeneic hematopoietic cell transplantation from matched sibling donors: a 20-year experience with the fractionated total body irradiation–etoposide regimen

Blood, 2008-08, Vol.112 (3), p.903-909

2008

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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 the Clinical Genome Resource (ClinGen)

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

A Clinicopathologic and Molecular Analysis of 34 Mediastinal Germ Cell Tumors Suggesting Different Modes of Teratoma Development

Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

Is it time to sound an alarm about false-positive cell-free DNA testing for fetal aneuploidy?

Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings

Loss of SMARCB1/INI1 expression in poorly differentiated chordomas

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 (ACMG) and the Clinical Genome Resource (ClinGen)

Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study

Still a screening test: more attention needed to noninvasive prenatal test false-positive rates

Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials

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

Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes

Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?

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

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

Overexpression of the Anaphase Promoting Complex/Cyclosome Inhibitor Emi1 Leads to Tetraploidy and Genomic Instability of p53-Deficient Cells

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

HER2 expression in gastric and gastroesophageal junction adenocarcinoma in a US population: clinicopathologic analysis with proposed approach to HER2 assessment

Terminal deletion of 6p results in a recognizable phenotype

Immune checkpoint blockade as a potential therapeutic strategy for undifferentiated malignancies

Acute leukemia in a patient with 15q overgrowth syndrome

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

Investigating human placentation and pregnancy using first trimester chorionic villi

Long-term remission of Philadelphia chromosome–positive acute lymphoblastic leukemia after allogeneic hematopoietic cell transplantation from matched sibling donors: a 20-year experience with the fractionated total body irradiation–etoposide regimen

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