Publications by authors named "Carla Rosenberg"

99Publications

Cytogenetically visible inversions are formed by multiple molecular mechanisms.

Hum Mutat 2020 Nov 1;41(11):1979-1998. Epub 2020 Oct 1.

Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

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http://dx.doi.org/10.1002/humu.24106DOI Listing
November 2020

Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing.

Ann Hum Genet 2020 Aug 6. Epub 2020 Aug 6.

The Human Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1111/ahg.12402DOI Listing
August 2020

Expanding the role of SETD5 haploinsufficiency in neurodevelopment and neuroblastoma.

Pediatr Blood Cancer 2020 Aug 3:e28376. Epub 2020 Aug 3.

Human Genome and Stem-Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1002/pbc.28376DOI Listing
August 2020

Genetic investigation of patients with tall stature.

Eur J Endocrinol 2020 Feb;182(2):139-147

Unidade de Endocrinologia Genética (LIM25), Laboratório de Hormônios e Genética Molecular (LIM42), Hospital das Clínicas da Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, Brasil.

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http://dx.doi.org/10.1530/EJE-19-0785DOI Listing
February 2020

Atypical presentation of a germline APC mutation in a child with supratentorial primitive neuroectodermal tumor.

Pediatr Blood Cancer 2019 04 4;66(4):e27566. Epub 2018 Dec 4.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1002/pbc.27566DOI Listing
April 2019

Increased DNA Copy Number Variation Mosaicism in Elderly Human Brain.

Neural Plast 2018 28;2018:2406170. Epub 2018 Jun 28.

Human Genome and Stem Cells Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão 277, 05508-090 São Paulo, SP, Brazil.

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http://dx.doi.org/10.1155/2018/2406170DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6046114PMC
December 2018

A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts.

Stem Cell Res 2018 08 4;31:52-54. Epub 2018 Jul 4.

Department of Genetics and Evolutionary Biology, Human Genome and Stem Cell Research Center, Biosciences Institute, University of São Paulo (USP), São Paulo, SP 05508-900, Brazil. Electronic address:

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http://dx.doi.org/10.1016/j.scr.2018.07.002DOI Listing
August 2018

Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion.

Chromosome Res 2018 09 12;26(3):191-198. Epub 2018 May 12.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão 277, Sao Paulo, SP, 05508-090, Brazil.

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http://link.springer.com/10.1007/s10577-018-9578-z
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http://dx.doi.org/10.1007/s10577-018-9578-zDOI Listing
September 2018

KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability.

Hum Genome Var 2018 29;5:18010. Epub 2018 Mar 29.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

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http://www.nature.com/articles/hgv201810
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http://dx.doi.org/10.1038/hgv.2018.10DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694292PMC
March 2018

Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes.

Clin Endocrinol (Oxf) 2018 03 10;88(3):425-431. Epub 2018 Jan 10.

Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormônios e Genética Molecular LIM42, Hospital das Clínicas, Disciplina de Endocrinologia, Faculdade de Medicina da Universidade de São Paulo, Sao Paulo, Brasil.

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http://dx.doi.org/10.1111/cen.13535DOI Listing
March 2018

Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause.

Horm Res Paediatr 2018 9;89(1):13-21. Epub 2017 Nov 9.

Unidade de Endocrinologia Genetica, Laboratorio de Endocrinologia Celular e Molecular LIM25, Disciplina de Endocrinologia da Faculdade de Medicina da Universidade de Sao Paulo (FMUSP), Sao Paulo, Brazil.

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http://dx.doi.org/10.1159/000481777DOI Listing
October 2018

Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting.

Eur J Med Genet 2017 Dec 4;60(12):667-674. Epub 2017 Sep 4.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão 277, 05508-090, São Paulo, SP, Brazil.

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http://dx.doi.org/10.1016/j.ejmg.2017.08.020DOI Listing
December 2017

Interstitial 1q21.1 Microdeletion Is Associated with Severe Skeletal Anomalies, Dysmorphic Face and Moderate Intellectual Disability.

Mol Syndromol 2016 Nov 26;7(6):344-348. Epub 2016 Oct 26.

Department of Clinical Genetics, Hospital for Rehabilitation of Craniofacial Anomalies (HRCA), University of São Paulo, Bauru, Brazil.

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http://dx.doi.org/10.1159/000450971DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131332PMC
November 2016

Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer's Disease?

Front Genet 2016 14;7:107. Epub 2016 Jun 14.

Human Genome and Stem-Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo Brazil.

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http://dx.doi.org/10.3389/fgene.2016.00107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905985PMC
July 2016

Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer's Disease Individuals.

Neural Plast 2016 26;2016:2584940. Epub 2016 Apr 26.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão 277, 05508-090 São Paulo, SP, Brazil.

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http://dx.doi.org/10.1155/2016/2584940DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861808PMC
December 2016

Partial 1q Duplications and Associated Phenotype.

Mol Syndromol 2016 Feb 4;6(6):297-303. Epub 2016 Feb 4.

Programa de Pós-graduação em Ciências da Saúde, São Paulo, Brazil; Faculdade de Medicina, Universidade de Brasília, São Paulo, Brazil.

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http://dx.doi.org/10.1159/000443599DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4803000PMC
February 2016

Role of rare germline copy number variation in melanoma-prone patients.

Future Oncol 2016 Jun 29;12(11):1345-57. Epub 2016 Mar 29.

Department of Genetics & Evolutionary Biology, Institute of Biosciences, University of São Paulo, Brazil.

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http://dx.doi.org/10.2217/fon.16.22DOI Listing
June 2016

Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?

Am J Med Genet A 2016 Feb 14;170A(2):403-409. Epub 2015 Nov 14.

Programa de Graduação em Biotecnologia, Centro de Ciências da Saúde, Universidade Federal do Espírito Santo (UFES), Vitória, Espírito Santo, Brasil.

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http://dx.doi.org/10.1002/ajmg.a.37448DOI Listing
February 2016

DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma Patients.

Biomed Res Int 2015 12;2015:376423. Epub 2015 Apr 12.

International Research Center, A.C.Camargo Cancer Center, Rua Taguá 440, 01508010 São Paulo, SP, Brazil ; Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão 277, 05508090 São Paulo, SP, Brazil.

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http://dx.doi.org/10.1155/2015/376423DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4461735PMC
March 2016

Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies.

Mol Genet Genomics 2015 Dec 4;290(6):2213-6. Epub 2015 Jun 4.

Department of Genetics, Institute of Biosciences, University of São Paulo State, Botucatu, SP, Brazil.

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http://link.springer.com/10.1007/s00438-015-1072-0
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http://dx.doi.org/10.1007/s00438-015-1072-0DOI Listing
December 2015

Novel partial duplication of EYA1 causes branchiootic syndrome in a large Brazilian family.

Int J Audiol 2015 30;54(9):593-8. Epub 2015 Apr 30.

* Department of Genetics and Evolutionary Biology, Biosciences Institute, University of São Paulo , Brazil.

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http://dx.doi.org/10.3109/14992027.2015.1030511DOI Listing
May 2016

Cleft lip/palate, short stature, and developmental delay in a boy with a 5.6-mb interstitial deletion involving 10p15.3p14.

Mol Syndromol 2015 Feb 22;6(1):39-43. Epub 2015 Jan 22.

Department of Genetics, Institute of Biosciences, São Paulo, Brazil ; Department of Genetics, Institute of Biosciences, Federal University of Goias, Goiânia, Brazil.

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http://dx.doi.org/10.1159/000371404DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369120PMC
February 2015

Subtelomeric 6p25 deletion/duplication: Report of a patient with new clinical findings and genotype-phenotype correlations.

Eur J Med Genet 2015 May 24;58(5):310-8. Epub 2015 Mar 24.

Departamento de Propedêutica Complementar, Faculdade de Medicina, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

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http://dx.doi.org/10.1016/j.ejmg.2015.02.011DOI Listing
May 2015

LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis.

Melanoma Res 2015 Apr;25(2):173-7

aInternational Research Center bDepartment of Oncogenetics cSkin Cancer Department, A. C. Camargo Cancer Center dDepartment of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo eFederal Technological University of Paraná, Paraná, Brazil.

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http://dx.doi.org/10.1097/CMR.0000000000000141DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352068PMC
April 2015

Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas.

Future Oncol 2014 Dec;10(15):2449-57

Department of Genetics & Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.2217/fon.14.149DOI Listing
December 2014

Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.

Am J Hum Genet 2014 Nov 6;95(5):565-78. Epub 2014 Nov 6.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.10.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225592PMC
November 2014

Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutations.

Exp Mol Pathol 2014 Dec 16;97(3):425-32. Epub 2014 Sep 16.

International Center for Research, A. C. Camargo Cancer Center, Sao Paulo, Brazil; Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of Sao Paulo, Sao Paulo, Brazil. Electronic address:

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http://dx.doi.org/10.1016/j.yexmp.2014.09.009DOI Listing
December 2014

A microdeletion in Alzheimer's disease disrupts NAMPT gene.

J Genet 2014 Aug;93(2):535-7

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matáo 277, 05508-090, Sáo Paulo, Brazil.

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http://dx.doi.org/10.1007/s12041-014-0399-3DOI Listing
August 2014

Genome-wide screening of copy number variants in children born small for gestational age reveals several candidate genes involved in growth pathways.

Eur J Endocrinol 2014 Aug 30;171(2):253-62. Epub 2014 May 30.

Unidade de Endocrinologia GeneticaLaboratorio de Endocrinologia Celular e Molecular LIM/25, Disciplina de Endocrinologia da Faculdade de Medicina da Universidade de Sao Paulo, Av. Dr. Arnaldo, 455 5° Andar Sala 5340, CEP 01246-903 Sao Paulo, BrazilDepartamento de Genetica e Biologia EvolutivaInstituto de Biociencias da Universidade de Sao Paulo, 05508-900 Sao Paulo, BrazilUnidade de GeneticaInstituto da Crianca, Faculdade de Medicina da Universidade de Sao Paulo, 05403-000 Sao Paulo, BrazilUnidade de Endocrinologia do DesenvolvimentoLaboratorio de Hormonios e Genetica Molecular LIM/42 do Hospital das Clinicas, Disciplina de Endocrinologia da Faculdade de Medicina da Universidade de Sao Paulo, 05403-900 Sao Paulo, Brazil

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http://dx.doi.org/10.1530/EJE-14-0232DOI Listing
August 2014

The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations.

Orphanet J Rare Dis 2014 Apr 28;9:63. Epub 2014 Apr 28.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão, 277-05422-970 São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1186/1750-1172-9-63DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022048PMC
April 2014

Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss.

Eur J Med Genet 2014 Mar 18;57(4):125-8. Epub 2014 Feb 18.

Department of Genetics and Evolutionary Biology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212140003
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http://dx.doi.org/10.1016/j.ejmg.2014.02.006DOI Listing
March 2014

Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum.

Am J Med Genet A 2014 Feb 5;164A(2):551-3. Epub 2013 Dec 5.

Programa de Pós-Graduação em Ciências da Saúde, Universidade de Brasília, DF, Brazil; Laboratório de Genética, Departamento de Genética e Morfologia, Instituto de, Ciências Biológicas Universidade de Brasília, Brasília, DF, Brazil.

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http://dx.doi.org/10.1002/ajmg.a.36231DOI Listing
February 2014

Array-CGH as an adjuvant tool in cytogenetic diagnosis of pediatric MDS and JMML.

Med Oncol 2013 Dec 2;30(4):734. Epub 2013 Oct 2.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão, 277, São Paulo, 05508-090, Brazil,

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http://dx.doi.org/10.1007/s12032-013-0734-1DOI Listing
December 2013

Single-nucleotide polymorphism-array improves detection rate of genomic alterations in core-binding factor leukemia.

Med Oncol 2013 1;30(2):579. Epub 2013 May 1.

Division of Hematology and Hemotherapy, UNIFESP/Escola Paulista de Medicina, São Paulo, SP, CEP: 04037-002, Brazil.

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http://dx.doi.org/10.1007/s12032-013-0579-7DOI Listing
October 2013

A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate.

Eur J Med Genet 2013 Apr 8;56(4):222-5. Epub 2013 Feb 8.

Department of Genetics and Evolutionary Biology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1016/j.ejmg.2013.01.002DOI Listing
April 2013

Molecular and clinical delineation of the 17q22 microdeletion phenotype.

Eur J Hum Genet 2013 Oct 30;21(10):1085-92. Epub 2013 Jan 30.

1] Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden [2] Department of Molecular Medicine and Surgery and Center of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden [3] Department of Hand Surgery, Södersjukhuset, Stockholm, Sweden.

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http://www.nature.com/articles/ejhg2012306
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http://dx.doi.org/10.1038/ejhg.2012.306DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778344PMC
October 2013

Number of rare germline CNVs and TP53 mutation types.

Orphanet J Rare Dis 2012 Dec 21;7:101. Epub 2012 Dec 21.

International Center for Research and Training, A.C. Camaargo Hospital, São Paulo, Brazil.

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http://dx.doi.org/10.1186/1750-1172-7-101DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558401PMC
December 2012

A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state.

Eur J Med Genet 2012 Nov 20;55(11):660-5. Epub 2012 Jul 20.

Department of Medical Genetics, Faculty of Medical Sciences, University of Campinas, Rua Tessália Vieira de Camargo, 126 CEP 13083-887 Campinas, São Paulo, Brazil.

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http://dx.doi.org/10.1016/j.ejmg.2012.06.015DOI Listing
November 2012

Germline copy number variations and cancer predisposition.

Future Oncol 2012 Apr;8(4):441-50

CIPE, AC Camargo Hospital, São Paulo, Brazil.

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http://dx.doi.org/10.2217/fon.12.34DOI Listing
April 2012

Germline DNA copy number variation in familial and early-onset breast cancer.

Breast Cancer Res 2012 Feb 7;14(1):R24. Epub 2012 Feb 7.

National Institute of Science and Technology in Oncogenomics, AC Camargo Hospital, Rua Taguá 440, 01508-010, São Paulo, Brazil.

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http://dx.doi.org/10.1186/bcr3109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496142PMC
February 2012

Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy.

Epilepsia 2010 Dec 30;51(12):2457-60. Epub 2010 Sep 30.

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1111/j.1528-1167.2010.02742.xDOI Listing
December 2010

A novel de novo microdeletion spanning the SYNGAP1 gene on the short arm of chromosome 6 associated with mental retardation.

Am J Med Genet A 2010 Sep;152A(9):2376-8

Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of S~ao Paulo, S~ao Paulo, Brazil.

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http://dx.doi.org/10.1002/ajmg.a.33554DOI Listing
September 2010

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.

Genet Med 2007 Sep;9(9):600-6

Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115 , USA.

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http://dx.doi.org/10.1097/gim.0b013e318149e1e3DOI Listing
September 2007

Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndrome.

Am J Med Genet A 2007 Aug;143A(15):1790-5

Centro de Estudos do Genoma Humano, Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1002/ajmg.a.31661DOI Listing
August 2007

Ring chromosome formation as a novel escape mechanism in patients with inverted duplication and terminal deletion.

Eur J Hum Genet 2007 May 7;15(5):548-55. Epub 2007 Mar 7.

Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1038/sj.ejhg.5201807DOI Listing
May 2007

Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and array-CGH.

Am J Med Genet A 2007 Mar;143A(6):610-4

Center for Human and Clinical Genetics, Leiden University Medical Center, RC Leiden, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.31593DOI Listing
March 2007

Detection and molecular cytogenetic characterization of a novel ring chromosome in a histological variant of Ewing sarcoma.

Cancer Genet Cytogenet 2007 Jan;172(1):12-22

Department of Molecular Cell Biology, Leiden University Medical Center, Post Zone S-01-P, PO Box 9600, 2300RC Leiden, The Netherlands.

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http://linkinghub.elsevier.com/retrieve/pii/S016546080600469
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http://dx.doi.org/10.1016/j.cancergencyto.2006.07.007DOI Listing
January 2007

Molecular cytogenetic characterization of four previously established and two newly established Ewing sarcoma cell lines.

Cancer Genet Cytogenet 2006 Apr;166(2):173-9

Department of Molecular Cell Biology, Leiden University Medical Center, PO Box 9600, 2300RC, Leiden, The Netherlands.

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http://dx.doi.org/10.1016/j.cancergencyto.2005.11.006DOI Listing
April 2006

Chromosomal instability in MYH- and APC-mutant adenomatous polyps.

Cancer Res 2006 Mar;66(5):2514-9

Department of Pathology, Josephine Nefkens Institute, Rotterdam, the Netherlands.

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http://dx.doi.org/10.1158/0008-5472.CAN-05-2407DOI Listing
March 2006

An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome.

Am J Med Genet A 2005 Dec;139(3):221-6

Centro de Estudos do Genoma Humano, Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.

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http://dx.doi.org/10.1002/ajmg.a.30991DOI Listing
December 2005

Array CGH detection of a cryptic deletion in a complex chromosome rearrangement.

Hum Genet 2005 Apr 22;116(5):390-4. Epub 2005 Feb 22.

Laboratory of Cytochemistry and Cytometry, Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1007/s00439-004-1248-xDOI Listing
April 2005

Insights from genomic microarrays into structural chromosome rearrangements.

Am J Med Genet A 2005 Jan;132A(1):36-40

Laboratory for Cytochemistry and Cytometry, Department of Molecular Cell Biology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.30378DOI Listing
January 2005

Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH.

Nucleic Acids Res 2004 Oct 28;32(19):e146. Epub 2004 Oct 28.

Department of Pathology, Josephine Nefkens Institute, Erasmus University Medical Center, Rotterdam, The Netherlands.

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http://dx.doi.org/10.1093/nar/gnh142DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC528818PMC
October 2004

Multicolor fluorescence in situ hybridization analysis of a synovial sarcoma of the larynx with a t(X;18)(p11.2;q11.2) and trisomies 2 and 8.

Cancer Genet Cytogenet 2004 Aug;153(1):48-52

Department of Molecular Cell Biology, Leiden University Medical Center, Albinusdreef2, 2333ZA Leiden, The Netherlands.

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http://dx.doi.org/10.1016/j.cancergencyto.2003.12.012DOI Listing
August 2004

Array comparative genomic hybridization with cyanin cis-platinum-labeled DNAs.

Biotechniques 2004 Jul;37(1):130-4

Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.2144/04371DD03DOI Listing
July 2004

A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B gene.

Cancer Genet Cytogenet 2004 Feb;149(1):72-6

Laboratory of Cytochemistry and Cytometry, Department of Molecular Cell Biology, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands.

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http://dx.doi.org/10.1016/s0165-4608(03)00302-9DOI Listing
February 2004

Multiple supernumerary ring chromosomes of different origin in a patient: a clinical report and review of the literature.

Am J Med Genet A 2003 Oct;122A(2):168-73

Clinical Genetic Center, Leiden University Medical Center (LUMC), Leiden, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.20163DOI Listing
October 2003

Application of multicolor fluorescence in situ hybridization analysis for detection of cross-contamination and in vitro progression in commonly used murine tumor cell lines.

Cancer Genet Cytogenet 2002 Dec;139(2):126-32

Laboratory for Cytochemistry and Cytometry, Department Molecular Cell Biology, Leiden University Medical Center, 2333 AL, Leiden, The Netherlands.

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http://dx.doi.org/10.1016/s0165-4608(02)00623-4DOI Listing
December 2002

Spectrum of genetic changes in gastro-esophageal cancer cell lines determined by an integrated molecular cytogenetic approach.

Cancer Genet Cytogenet 2002 May;135(1):35-41

Laboratory of Cytochemistry and Cytometry, Department Molecular Cell Biology, Leiden University Medical Center (LUMC), Leiden, The Netherlands.

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http://dx.doi.org/10.1016/s0165-4608(01)00639-2DOI Listing
May 2002