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Daniel Pinkel
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61
Albertson, Donna
41
Gray, Joe
19
Fridlyand, Jane
18
Segraves, Richard
16
Snijders, Antoine
16
Waldman, Frederic
15
Kuo, Wen-Lin
15
Collins, Colin
14
Bastian, Boris
14
Kallioniemi, Olli
13
Kallioniemi, Anne
11
Jain, Ajay
10
Sudar, Damir
9
van Dekken, Herman
8
Kowbel, David
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All Publications
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2008: Clark Steve M; Hamilton Gregory E; Nordmeyer Robert A; Uber Donald; Cornell Earl W; Brown Nils; Segraves Richard; Davis Randy; Albertson Donna G; Pinkel Daniel
High-efficiency microarray printer using fused-silica capillary tube printing pins.
Analytical chemistry 2008;80(19):7639-42.
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2008: Bastian Boris C; Pinkel Daniel
Expanding the genetic spectrum of pigmentation.
Pigment cell & melanoma research 2008;21(5):507-8.
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2008: North Jeffrey P; Kageshita Toshiro; Pinkel Daniel; LeBoit Philip E; Bastian Boris C
Distribution and significance of occult intraepidermal tumor cells surrounding primary melanoma.
The Journal of investigative dermatology 2008;128(8):2024-30.
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2008: Viros Amaya; Fridlyand Jane; Bauer Juergen; Lasithiotakis Konstantin; Garbe Claus; Pinkel Daniel; Bastian Boris C
Improving melanoma classification by integrating genetic and morphologic features.
PLoS medicine 2008;5(6):e120.
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2008: Curtin John A; Pinkel Daniel; Bastian Boris C
Absence of PDGFRA mutations in primary melanoma.
The Journal of investigative dermatology 2008;128(2):488-9.
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2007: Herlyn Meenhard; Halaban Ruth; Ronai Ze'ev; Schuchter Lynn; Berwick Marianne; Pinkel Daniel
Roadmap for new opportunities in melanoma research.
Seminars in oncology 2007;34(6):566-76.
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2007: Pinkel Daniel
Analytical description of mutational effects in competing asexual populations.
Genetics 2007;177(4):2135-49.
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2007: Mefford Heather C; Clauin Severine; Sharp Andrew J; Moller Rikke S; Ullmann Reinhard; Kapur Raj; Pinkel Dan; Cooper Gregory M; Ventura Mario; Ropers H Hilger; Tommerup Niels; Eichler Evan E; Bellanne-Chantelot Christine
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.
American journal of human genetics 2007;81(5):1057-69.
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2007: Tokuyasu Taku A; Cotter Philip D; Segraves Richard; Harris Jeffrey; Elder Melissa E; Gonzales Marcos; Pinkel Daniel; Albertson Donna G; Rauen Katherine A
Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system.
American journal of medical genetics. Part A 2007;143A(9):925-32.
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2007: Climent Joan; Dimitrow Peter; Fridlyand Jane; Palacios Jose; Siebert Reiner; Albertson Donna G; Gray Joe W; Pinkel Daniel; Lluch Ana; Martinez-Climent Jose A
Deletion of chromosome 11q predicts response to anthracycline-based chemotherapy in early breast cancer.
Cancer research 2007;67(2):818-26.
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2007: Thorns Christoph; Bastian Boris; Pinkel Daniel; Roydasgupta Ritu; Fridlyand Jane; Merz Hartmut; Krokowski Manuela; Bernd Heinz-Wolfram; Feller Alfred Christian
Chromosomal aberrations in angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma unspecified: A matrix-based CGH approach.
Genes, chromosomes & cancer 2007;46(1):37-44.
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2007: Mestre-Escorihuela Cinta; Rubio-Moscardo Fanny; Richter Jose A; Siebert Reiner; Climent Joan; Fresquet Vicente; Beltran Elena; Agirre Xabier; Marugan Isabel; Marín Miguel; Rosenwald Andreas; Sugimoto Kei-Ji; Wheat Luise M; Karran E Loraine; García Juan F; Sanchez Lydia; Prosper Felipe; Staudt Louis M; Pinkel Daniel; Dyer Martin J S; Martinez-Climent Jose A
Homozygous deletions localize novel tumor suppressor genes in B-cell lymphomas.
Blood 2007;109(1):271-80.
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2007: Bauer Jürgen; Curtin John A; Pinkel Dan; Bastian Boris C
Congenital melanocytic nevi frequently harbor NRAS mutations but no BRAF mutations.
The Journal of investigative dermatology 2007;127(1):179-82.
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2007: Gajduskova Pavla; Snijders Antoine M; Kwek Serena; Roydasgupta Ritu; Fridlyand Jane; Tokuyasu Taku; Pinkel Daniel; Albertson Donna G
Genome position and gene amplification.
Genome biology 2007;8(6):R120.
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2006: Chin Koei; DeVries Sandy; Fridlyand Jane; Spellman Paul T; Roydasgupta Ritu; Kuo Wen-Lin; Lapuk Anna; Neve Richard M; Qian Zuwei; Ryder Tom; Chen Fanqing; Feiler Heidi; Tokuyasu Taku; Kingsley Chris; Dairkee Shanaz; Meng Zhenhang; Chew Karen; Pinkel Daniel; Jain Ajay; Ljung Britt Marie; Esserman Laura; Albertson Donna G; Waldman Frederic M; Gray Joe W
Genomic and transcriptional aberrations linked to breast cancer pathophysiologies.
Cancer cell 2006;10(6):529-41.
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2006: Neve Richard M; Chin Koei; Fridlyand Jane; Yeh Jennifer; Baehner Frederick L; Fevr Tea; Clark Laura; Bayani Nora; Coppe Jean-Philippe; Tong Frances; Speed Terry; Spellman Paul T; DeVries Sandy; Lapuk Anna; Wang Nick J; Kuo Wen-Lin; Stilwell Jackie L; Pinkel Daniel; Albertson Donna G; Waldman Frederic M; McCormick Frank; Dickson Robert B; Johnson Michael D; Lippman Marc; Ethier Stephen; Gazdar Adi; Gray Joe W
A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes.
Cancer cell 2006;10(6):515-27.
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2006: Stransky Nicolas; Vallot Céline; Reyal Fabien; Bernard-Pierrot Isabelle; de Medina Sixtina Gil Diez; Segraves Rick; de Rycke Yann; Elvin Paul; Cassidy Andrew; Spraggon Carolyn; Graham Alexander; Southgate Jennifer; Asselain Bernard; Allory Yves; Abbou Claude C; Albertson Donna G; Thiery Jean Paul; Chopin Dominique K; Pinkel Daniel; Radvanyi François
Regional copy number-independent deregulation of transcription in cancer.
Nature genetics 2006;38(12):1386-96.
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2006: Curtin John A; Busam Klaus; Pinkel Daniel; Bastian Boris C
Somatic activation of KIT in distinct subtypes of melanoma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2006;24(26):4340-6.
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2006: Sharp Andrew J; Hansen Sierra; Selzer Rebecca R; Cheng Ze; Regan Regina; Hurst Jane A; Stewart Helen; Price Sue M; Blair Edward; Hennekam Raoul C; Fitzpatrick Carrie A; Segraves Rick; Richmond Todd A; Guiver Cheryl; Albertson Donna G; Pinkel Daniel; Eis Peggy S; Schwartz Stuart; Knight Samantha J L; Eichler Evan E
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
Nature genetics 2006;38(9):1038-42.
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2006: Locke Devin P; Sharp Andrew J; McCarroll Steven A; McGrath Sean D; Newman Tera L; Cheng Ze; Schwartz Stuart; Albertson Donna G; Pinkel Daniel; Altshuler David M; Eichler Evan E
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
American journal of human genetics 2006;79(2):275-90.
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2006: Landi Maria Teresa; Bauer Jürgen; Pfeiffer Ruth M; Elder David E; Hulley Benjamin; Minghetti Paola; Calista Donato; Kanetsky Peter A; Pinkel Daniel; Bastian Boris C
MC1R germline variants confer risk for BRAF-mutant melanoma.
Science (New York, N.Y.) 2006;313(5786):521-2.
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2006: Curtin John A; Stark Mitchell S; Pinkel Daniel; Hayward Nicholas K; Bastian Boris C
PI3-kinase subunits are infrequent somatic targets in melanoma.
The Journal of investigative dermatology 2006;126(7):1660-3.
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2006: Albertson Donna G; Snijders Antoine M; Fridlyand Jane; Jordan Richard; Pinkel Daniel; Schmidt Brian L
Genomic analysis of tumors by array comparative genomic hybridization: more is better.
Cancer research 2006;66(7):3955-6; author reply 3956.
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2006: Li Marilyn; Pinkel Daniel
Clinical cytogenetics and molecular cytogenetics.
Journal of Zhejiang University. Science. B 2006;7(2):162-3.
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2006: Iglesias Alejandro; Rauen Katherine A; Albertson Donna G; Pinkel Daniel; Cotter Philip D
Duplication of distal 20q: clinical, cytogenetic and array CGH. Characterization of a new case.
Clinical dysmorphology 2006;15(1):19-23.
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2006: Glass Ian A; Rauen Katherine A; Chen Emily; Parkes Jillian; Alberston Donna G; Pinkel Daniel; Cotter Philip D
Ring chromosome 15: characterization by array CGH.
Human genetics 2006;118(5):611-7.
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2006: Hamilton G; Brown N; Oseroff V; Huey B; Segraves R; Sudar D; Kumler J; Albertson D; Pinkel D
A large field CCD system for quantitative imaging of microarrays.
Nucleic acids research 2006;34(8):e58.
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2006: Fridlyand Jane; Snijders Antoine M; Ylstra Bauke; Li Hua; Olshen Adam; Segraves Richard; Dairkee Shanaz; Tokuyasu Taku; Ljung Britt Marie; Jain Ajay N; McLennan Jane; Ziegler John; Chin Koei; Devries Sandy; Feiler Heidi; Gray Joe W; Waldman Frederic; Pinkel Daniel; Albertson Donna G
Breast tumor copy number aberration phenotypes and genomic instability.
BMC cancer 2006;6():96.
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2005: Curtin John A; Fridlyand Jane; Kageshita Toshiro; Patel Hetal N; Busam Klaus J; Kutzner Heinz; Cho Kwang-Hyun; Aiba Setsuya; Bröcker Eva-Bettina; LeBoit Philip E; Pinkel Dan; Bastian Boris C
Distinct sets of genetic alterations in melanoma.
The New England journal of medicine 2005;353(20):2135-47.
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2005: Sherr E H; Owen R; Albertson D G; Pinkel D; Cotter P D; Slavotinek A M; Hetts S W; Jeremy R J; Schilmoeller G; Schilmoeller K; Wakahiro M; Barkovich A J
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies.
Neurology 2005;65(9):1496-8.
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2005: Klein Ophir D; Cotter Philip D; Schmidt Ann M; Bick David P; Tidyman William E; Albertson Donna G; Pinkel Daniel; Rauen Katherine A
Interstitial deletion of chromosome 12q: genotype-phenotype correlation of two patients utilizing array comparative genomic hybridization.
American journal of medical genetics. Part A 2005;138(4):349-54.
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2005: Rubio-Moscardo Fanny; Blesa David; Mestre Cinta; Siebert Reiner; Balasas Theo; Benito Adalberto; Rosenwald Andreas; Climent Joan; Martinez Jose I; Schilhabel Markus; Karran E Lorraine; Gesk Stefan; Esteller Manel; deLeeuw Ronald; Staudt Louis M; Fernandez-Luna Jose Luis; Pinkel Daniel; Dyer Martin J S; Martinez-Climent Jose A
Characterization of 8p21.3 chromosomal deletions in B-cell lymphoma: TRAIL-R1 and TRAIL-R2 as candidate dosage-dependent tumor suppressor genes.
Blood 2005;106(9):3214-22.
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2005: Sharp Andrew J; Locke Devin P; McGrath Sean D; Cheng Ze; Bailey Jeffrey A; Vallente Rhea U; Pertz Lisa M; Clark Royden A; Schwartz Stuart; Segraves Rick; Oseroff Vanessa V; Albertson Donna G; Pinkel Daniel; Eichler Evan E
Segmental duplications and copy-number variation in the human genome.
American journal of human genetics 2005;77(1):78-88.
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2005: Tuzun Eray; Sharp Andrew J; Bailey Jeffrey A; Kaul Rajinder; Morrison V Anne; Pertz Lisa M; Haugen Eric; Hayden Hillary; Albertson Donna; Pinkel Daniel; Olson Maynard V; Eichler Evan E
Fine-scale structural variation of the human genome.
Nature genetics 2005;37(7):727-32.
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2005: Pinkel Daniel; Albertson Donna G
Array comparative genomic hybridization and its applications in cancer.
Nature genetics 2005;37 Suppl():S11-7.
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2005: Ching Tsui-Ting; Maunakea Alika K; Jun Peter; Hong Chibo; Zardo Giuseppe; Pinkel Daniel; Albertson Donna G; Fridlyand Jane; Mao Jian-Hua; Shchors Ksenya; Weiss William A; Costello Joseph F
Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3.
Nature genetics 2005;37(6):645-51.
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2005: Cheng Sabrina F; Rauen Katherine A; Pinkel Daniel; Albertson Donna G; Cotter Philip D
Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.
American journal of medical genetics. Part A 2005;135(3):308-13.
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2005: Snijders Antoine M; Schmidt Brian L; Fridlyand Jane; Dekker Nusi; Pinkel Daniel; Jordan Richard C K; Albertson Donna G
Rare amplicons implicate frequent deregulation of cell fate specification pathways in oral squamous cell carcinoma.
Oncogene 2005;24(26):4232-42.
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2005: Rubio-Moscardo Fanny; Climent Joan; Siebert Reiner; Piris Miguel A; Martín-Subero Jose I; Nieländer Inga; Garcia-Conde Javier; Dyer Martin J S; Terol Maria Jose; Pinkel Daniel; Martinez-Climent Jose A
Mantle-cell lymphoma genotypes identified with CGH to BAC microarrays define a leukemic subgroup of disease and predict patient outcome.
Blood 2005;105(11):4445-54.
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2005: Misra Anjan; Pellarin Malgorzata; Nigro Janice; Smirnov Ivan; Moore Dan; Lamborn Kathleen R; Pinkel Daniel; Albertson Donna G; Feuerstein Burt G
Array comparative genomic hybridization identifies genetic subgroups in grade 4 human astrocytoma.
Clinical cancer research : an official journal of the American Association for Cancer Research 2005;11(8):2907-18.
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2005: Snijders Antoine M; Nowak Norma J; Huey Bing; Fridlyand Jane; Law Sindy; Conroy Jeffrey; Tokuyasu Taku; Demir Kubilay; Chiu Readman; Mao Jian-Hua; Jain Ajay N; Jones Steven J M; Balmain Allan; Pinkel Daniel; Albertson Donna G
Mapping segmental and sequence variations among laboratory mice using BAC array CGH.
Genome research 2005;15(2):302-11.
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2005: Hermsen Mario; Snijders Antoine; Guervós Marta Alonso; Taenzer Simone; Koerner Ulrike; Baak Jan; Pinkel Daniel; Albertson Donna; van Diest Paul; Meijer Gerrit; Schrock Evelin
Centromeric chromosomal translocations show tissue-specific differences between squamous cell carcinomas and adenocarcinomas.
Oncogene 2005;24(9):1571-9.
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2005: Zhang Xiaoxiao; Snijders Antoine; Segraves Richard; Zhang Xiuqing; Niebuhr Anita; Albertson Donna; Yang Huanming; Gray Joe; Niebuhr Erik; Bolund Lars; Pinkel Dan
High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization.
American journal of human genetics 2005;76(2):312-26.
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2005: Pinkel Daniel; Albertson Donna G
Comparative genomic hybridization.
Annual review of genomics and human genetics 2005;6():331-54.
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2005: van Duin Mark; van Marion Ronald; Watson J E Vivienne; Paris Pamela L; Lapuk Anna; Brown Nils; Oseroff Vanessa V; Albertson Donna G; Pinkel Daniel; de Jong Pieter; Nacheva Elizabeth P; Dinjens Winand; van Dekken Herman; Collins Colin
Construction and application of a full-coverage, high-resolution, human chromosome 8q genomic microarray for comparative genomic hybridization.
Cytometry. Part A : the journal of the International Society for Analytical Cytology 2005;63(1):10-9.
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2004: Paris Pamela L; Andaya Armann; Fridlyand Jane; Jain Ajay N; Weinberg Vivian; Kowbel David; Brebner John H; Simko Jeff; Watson J E Vivienne; Volik Stas; Albertson Donna G; Pinkel Daniel; Alers Janneke C; van der Kwast Theodorus H; Vissers Kees J; Schroder Fritz H; Wildhagen Mark F; Febbo Phillip G; Chinnaiyan Arul M; Pienta Kenneth J; Carroll Peter R; Rubin Mark A; Collins Colin; van Dekken Herman
Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors.
Human molecular genetics 2004;13(13):1303-13.
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2004: Klein O D; Cotter P D; Albertson D G; Pinkel D; Tidyman W E; Moore M W; Rauen K A
Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
Clinical genetics 2004;65(6):477-82.
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2004: Watson J E Vivienne; Doggett Norman A; Albertson Donna G; Andaya Armann; Chinnaiyan Arul; van Dekken Herman; Ginzinger David; Haqq Christopher; James Karen; Kamkar Sherwin; Kowbel David; Pinkel Daniel; Schmitt Lars; Simko Jeffry P; Volik Stanislav; Weinberg Vivian K; Paris Pamela L; Collins Colin
Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23-qter and identifies underlying candidate tumor suppressor genes in prostate cancer.
Oncogene 2004;23(19):3487-94.
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2004: Locke D P; Segraves R; Nicholls R D; Schwartz S; Pinkel D; Albertson D G; Eichler E E
BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications.
Journal of medical genetics 2004;41(3):175-82.
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2004: Ishkanian Adrian S; Malloff Chad A; Watson Spencer K; DeLeeuw Ronald J; Chi Bryan; Coe Bradley P; Snijders Antoine; Albertson Donna G; Pinkel Daniel; Marra Marco A; Ling Victor; MacAulay Calum; Lam Wan L
A tiling resolution DNA microarray with complete coverage of the human genome.
Nature genetics 2004;36(3):299-303.
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2004: van Dekken Herman; Paris Pamela L; Albertson Donna G; Alers Janneke C; Andaya Armann; Kowbel David; van der Kwast Theodorus H; Pinkel Daniel; Schröder Fritz H; Vissers Kees J; Wildhagen Mark F; Collins Colin
Evaluation of genetic patterns in different tumor areas of intermediate-grade prostatic adenocarcinomas by high-resolution genomic array analysis.
Genes, chromosomes & cancer 2004;39(3):249-56.
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2004: Simin Karl; Wu Hua; Lu Lucy; Pinkel Dan; Albertson Donna; Cardiff Robert D; Van Dyke Terry
pRb inactivation in mammary cells reveals common mechanisms for tumor initiation and progression in divergent epithelia.
PLoS biology 2004;2(2):E22.
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2004: Weiss Marjan M; Kuipers Ernst J; Postma Cindy; Snijders Antoine M; Pinkel Daniel; Meuwissen Stefan G M; Albertson Donna; Meijer Gerrit A
Genomic alterations in primary gastric adenocarcinomas correlate with clinicopathological characteristics and survival.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2004;26(5-6):307-17.
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2004: Snijders Antoine M; Segraves Richard; Blackwood Stephanie; Pinkel Daniel; Albertson Donna G
BAC microarray-based comparative genomic hybridization.
Methods in molecular biology (Clifton, N.J.) 2004;256():39-56.
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2003: Maldonado Janet L; Fridlyand Jane; Patel Hetal; Jain Ajay N; Busam Klaus; Kageshita Toshiro; Ono Tomomichi; Albertson Donna G; Pinkel Dan; Bastian Boris C
Determinants of BRAF mutations in primary melanomas.
Journal of the National Cancer Institute 2003;95(24):1878-90.
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2003: Bastian Boris C; Olshen Adam B; LeBoit Philip E; Pinkel Daniel
Classifying melanocytic tumors based on DNA copy number changes.
The American journal of pathology 2003;163(5):1765-70.
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2003: Weiss M M; Kuipers E J; Postma C; Snijders A M; Stolte M; Vieth M; Pinkel D; Meuwissen S G M; Albertson D; Meijer G A
Genome wide array comparative genomic hybridisation analysis of premalignant lesions of the stomach.
Molecular pathology : MP 2003;56(5):293-8.
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2003: Albertson Donna G; Pinkel Daniel
Genomic microarrays in human genetic disease and cancer.
Human molecular genetics 2003;12 Spec No 2():R145-52.
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2003: Hackett Christopher S; Hodgson J Graeme; Law Mark E; Fridlyand Jane; Osoegawa Kazutoyo; de Jong Pieter J; Nowak Norma J; Pinkel Daniel; Albertson Donna G; Jain Ajay; Jenkins Robert; Gray Joe W; Weiss William A
Genome-wide array CGH analysis of murine neuroblastoma reveals distinct genomic aberrations which parallel those in human tumors.
Cancer research 2003;63(17):5266-73.
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2003: Snijders Antoine M; Fridlyand Jane; Mans Dorus A; Segraves Richard; Jain Ajay N; Pinkel Daniel; Albertson Donna G
Shaping of tumor and drug-resistant genomes by instability and selection.
Oncogene 2003;22(28):4370-9.
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2003: Weiss Marjan M; Snijders Antoine M; Kuipers Ernst J; Ylstra Bauke; Pinkel Daniel; Meuwissen Stefan G M; van Diest Paul J; Albertson Donna G; Meijer Gerrit A
Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization.
The Journal of pathology 2003;200(3):320-6.
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2003: Ki Anita; Rauen Katherine A; Black Lauri D; Kostiner Dana R; Sandberg Per L; Pinkel Daniel; Albertson Donna G; Norton Mary E; Cotter Philip D
Ring 21 chromosome and a satellited 1p in the same patient: novel origin for an ectopic NOR.
American journal of medical genetics. Part A 2003;120A(3):365-9.
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2003: Snijders Antoine M; Nowee Marlies E; Fridlyand Jane; Piek Jurgen M J; Dorsman Josephine C; Jain Ajay N; Pinkel Daniel; van Diest Paul J; Verheijen René H M; Albertson Donna G
Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in fallopian tube carcinoma.
Oncogene 2003;22(27):4281-6.
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2003: Veltman Joris A; Fridlyand Jane; Pejavar Sunanda; Olshen Adam B; Korkola James E; DeVries Sandy; Carroll Peter; Kuo Wen-Lin; Pinkel Daniel; Albertson Donna; Cordon-Cardo Carlos; Jain Ajay N; Waldman Frederic M
Array-based comparative genomic hybridization for genome-wide screening of DNA copy number in bladder tumors.
Cancer research 2003;63(11):2872-80.
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2003: Sanchez-Izquierdo Dolors; Buchonnet Gerard; Siebert Reiner; Gascoyne Randy D; Climent Joan; Karran Loraine; Marin Miguel; Blesa David; Horsman Douglas; Rosenwald Andreas; Staudt Louis M; Albertson Donna G; Du Ming-Qing; Ye Hongtao; Marynen Peter; Garcia-Conde Javier; Pinkel Daniel; Dyer Martin J S; Martinez-Climent Jose Angel
MALT1 is deregulated by both chromosomal translocation and amplification in B-cell non-Hodgkin lymphoma.
Blood 2003;101(11):4539-46.
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2003: Snijders Antoine M; Pinkel Daniel; Albertson Donna G
Current status and future prospects of array-based comparative genomic hybridisation.
Briefings in functional genomics & proteomics 2003;2(1):37-45.
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2003: Martinez-Climent Jose A; Alizadeh Ash A; Segraves Richard; Blesa David; Rubio-Moscardo Fanny; Albertson Donna G; Garcia-Conde Javier; Dyer Martin J S; Levy Ronald; Pinkel Daniel; Lossos Izidore S
Transformation of follicular lymphoma to diffuse large cell lymphoma is associated with a heterogeneous set of DNA copy number and gene expression alterations.
Blood 2003;101(8):3109-17.
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2003: Weiss Marjan M; Kuipers Ernst J; Postma Cindy; Snijders Antoine M; Siccama Ivar; Pinkel Daniel; Westerga Johan; Meuwissen Stefan G M; Albertson Donna G; Meijer Gerrit A
Genomic profiling of gastric cancer predicts lymph node status and survival.
Oncogene 2003;22(12):1872-9.
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2003: Locke Devin P; Segraves Richard; Carbone Lucia; Archidiacono Nicoletta; Albertson Donna G; Pinkel Daniel; Eichler Evan E
Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization.
Genome research 2003;13(3):347-57.
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2003: Paris Pamela L; Albertson Donna G; Alers Janneke C; Andaya Armann; Carroll Peter; Fridlyand Jane; Jain Ajay N; Kamkar Sherwin; Kowbel David; Krijtenburg Pieter-Jaap; Pinkel Daniel; Schröder Fritz H; Vissers Kees J; Watson Vivienne J E; Wildhagen Mark F; Collins Colin; Van Dekken Herman
High-resolution analysis of paraffin-embedded and formalin-fixed prostate tumors using comparative genomic hybridization to genomic microarrays.
The American journal of pathology 2003;162(3):763-70.
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2003: Lage José M; Leamon John H; Pejovic Tanja; Hamann Stefan; Lacey Michelle; Dillon Deborah; Segraves Richard; Vossbrinck Bettina; González Antonio; Pinkel Daniel; Albertson Donna G; Costa Jose; Lizardi Paul M
Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH.
Genome research 2003;13(2):294-307.
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2003: Kraus Jürgen; Pantel Klaus; Pinkel Daniel; Albertson Donna G; Speicher Michael R
High-resolution genomic profiling of occult micrometastatic tumor cells.
Genes, chromosomes & cancer 2003;36(2):159-66.
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2003: Gray Joe W; Suzuki Seiji; Kuo Wen-Lin; Polikoff Daniel; Deavers Michael; Smith-McCune Karen; Berchuck Andrew; Pinkel Dan; Albertson Donna; Mills Gordon B
Specific keynote: genome copy number abnormalities in ovarian cancer.
Gynecologic oncology 2003;88(1 Pt 2):S16-21; discussion S22-4.
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2002: Zardo Giuseppe; Tiirikainen Maarit I; Hong Chibo; Misra Anjan; Feuerstein Burt G; Volik Stanislav; Collins Colin C; Lamborn Kathleen R; Bollen Andrew; Pinkel Daniel; Albertson Donna G; Costello Joseph F
Integrated genomic and epigenomic analyses pinpoint biallelic gene inactivation in tumors.
Nature genetics 2002;32(3):453-8.
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2002: Bastian Boris C; Xiong Jessie; Frieden Ilona J; Williams Mary L; Chou Pauline; Busam Klaus; Pinkel Dan; LeBoit Philip E
Genetic changes in neoplasms arising in congenital melanocytic nevi: differences between nodular proliferations and melanomas.
The American journal of pathology 2002;161(4):1163-9.
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2002: Massion Pierre P; Kuo Wen-Lin; Stokoe David; Olshen Adam B; Treseler Patrick A; Chin Koei; Chen Chira; Polikoff Daniel; Jain Ajay N; Pinkel Daniel; Albertson Donna G; Jablons David M; Gray Joe W
Genomic copy number analysis of non-small cell lung cancer using array comparative genomic hybridization: implications of the phosphatidylinositol 3-kinase pathway.
Cancer research 2002;62(13):3636-40.
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2002: Rauen Katherine A; Albertson Donna G; Pinkel Daniel; Cotter Philip D
Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
American journal of medical genetics 2002;110(1):51-6.
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2002: Sauter Edward R; Yeo Un-Cheol; von Stemm Andrea; Zhu Weizhu; Litwin Samuel; Tichansky David S; Pistritto Giuseppa; Nesbit Mark; Pinkel Dan; Herlyn Meenhard; Bastian Boris C
Cyclin D1 is a candidate oncogene in cutaneous melanoma.
Cancer research 2002;62(11):3200-6.
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2002: Jain Ajay N; Tokuyasu Taku A; Snijders Antoine M; Segraves Richard; Albertson Donna G; Pinkel Daniel
Fully automatic quantification of microarray image data.
Genome research 2002;12(2):325-32.
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2001: Hodgson G; Hager J H; Volik S; Hariono S; Wernick M; Moore D; Nowak N; Albertson D G; Pinkel D; Collins C; Hanahan D; Gray J W
Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas.
Nature genetics 2001;29(4):459-64.
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2001: Snijders A M; Nowak N; Segraves R; Blackwood S; Brown N; Conroy J; Hamilton G; Hindle A K; Huey B; Kimura K; Law S; Myambo K; Palmer J; Ylstra B; Yue J P; Gray J W; Jain A N; Pinkel D; Albertson D G
Assembly of microarrays for genome-wide measurement of DNA copy number.
Nature genetics 2001;29(3):263-4.
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2001: DeVries S; Gray J W; Pinkel D; Waldman F M; Sudar D
Comparative genomic hybridization.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 4():Unit4.6.
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2000: Suzuki S; Moore D H; Ginzinger D G; Godfrey T E; Barclay J; Powell B; Pinkel D; Zaloudek C; Lu K; Mills G; Berchuck A; Gray J W
An approach to analysis of large-scale correlations between genome changes and clinical endpoints in ovarian cancer.
Cancer research 2000;60(19):5382-5.
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2000: Albertson D G; Ylstra B; Segraves R; Collins C; Dairkee S H; Kowbel D; Kuo W L; Gray J W; Pinkel D
Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene.
Nature genetics 2000;25(2):144-6.
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1999: Sternlicht M D; Lochter A; Sympson C J; Huey B; Rougier J P; Gray J W; Pinkel D; Bissell M J; Werb Z
The stromal proteinase MMP3/stromelysin-1 promotes mammary carcinogenesis.
Cell 1999;98(2):137-46.
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1999: Ortiz de Solórzano C; García Rodriguez E; Jones A; Pinkel D; Gray J W; Sudar D; Lockett S J
Segmentation of confocal microscope images of cell nuclei in thick tissue sections.
Journal of microscopy 1999;193(Pt 3):212-26.
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1999: Shayesteh L; Lu Y; Kuo W L; Baldocchi R; Godfrey T; Collins C; Pinkel D; Powell B; Mills G B; Gray J W
PIK3CA is implicated as an oncogene in ovarian cancer.
Nature genetics 1999;21(1):99-102.
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1998: Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo W L; Chen C; Zhai Y; Dairkee S H; Ljung B M; Gray J W; Albertson D G
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
Nature genetics 1998;20(2):207-11.
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1998: Collins C; Rommens J M; Kowbel D; Godfrey T; Tanner M; Hwang S I; Polikoff D; Nonet G; Cochran J; Myambo K; Jay K E; Froula J; Cloutier T; Kuo W L; Yaswen P; Dairkee S; Giovanola J; Hutchinson G B; Isola J; Kallioniemi O P; Palazzolo M; Martin C; Ericsson C; Pinkel D; Albertson D; Li W B; Gray J W
Positional cloning of ZNF217 and NABC1: genes amplified at 20q13.2 and overexpressed in breast carcinoma.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(15):8703-8.
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1998: Hiraguri S; Godfrey T; Nakamura H; Graff J; Collins C; Shayesteh L; Doggett N; Johnson K; Wheelock M; Herman J; Baylin S; Pinkel D; Gray J
Mechanisms of inactivation of E-cadherin in breast cancer cell lines.
Cancer research 1998;58(9):1972-7.
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1998: Lockett S J; Sudar D; Thompson C T; Pinkel D; Gray J W
Efficient, interactive, and three-dimensional segmentation of cell nuclei in thick tissue sections.
Cytometry 1998;31(4):275-86.
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1997: Yu L C; Moore D H; Magrane G; Cronin J; Pinkel D; Lebo R V; Gray J W
Objective aneuploidy detection for fetal and neonatal screening using comparative genomic hybridization (CGH).
Cytometry 1997;28(3):191-7.
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1997: Shi Y P; Naik P; Dietrich W F; Gray J W; Hanahan D; Pinkel D
DNA copy number changes associated with characteristic LOH in islet cell carcinomas of transgenic mice.
Genes, chromosomes & cancer 1997;19(2):104-11.
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1996: Ghazvini S; Char D H; Kroll S; Waldman F M; Pinkel D
Comparative genomic hybridization analysis of archival formalin-fixed paraffin-embedded uveal melanomas.
Cancer genetics and cytogenetics 1996;90(2):95-101.
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1995: Iwabuchi H; Sakamoto M; Sakunaga H; Ma Y Y; Carcangiu M L; Pinkel D; Yang-Feng T L; Gray J W
Genetic analysis of benign, low-grade, and high-grade ovarian tumors.
Cancer research 1995;55(24):6172-80.
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1995: Balazs M; Matsumura K; Moore D; Pinkel D; Gray J W; Waldman F M
Karyotypic heterogeneity and its relation to labeling index in interphase breast tumor cells.
Cytometry 1995;20(1):62-73.
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1995: Stokke T; Collins C; Kuo W L; Kowbel D; Shadravan F; Tanner M; Kallioniemi A; Kallioniemi O P; Pinkel D; Deaven L
A physical map of chromosome 20 established using fluorescence in situ hybridization and digital image analysis.
Genomics 1995;26(1):134-7.
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1995: Wyrobek A; Lowe X; Pinkel D; Bishop J
Aneuploidy in late-step spermatids of mice detected by two-chromosome fluorescence in situ hybridization.
Molecular reproduction and development 1995;40(2):259-66.
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1995: Sakamoto M; Pinkel D; Mascio L; Sudar D; Peters D; Kuo W L; Yamakawa K; Nakamura Y; Drabkin H; Jericevic Z
Semiautomated DNA probe mapping using digital imaging microscopy: II. System performance.
Cytometry 1995;19(1):60-9.
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1995: Piper J; Rutovitz D; Sudar D; Kallioniemi A; Kallioniemi O P; Waldman F M; Gray J W; Pinkel D
Computer image analysis of comparative genomic hybridization.
Cytometry 1995;19(1):10-26.
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1994: Kallioniemi O P; Kallioniemi A; Piper J; Isola J; Waldman F M; Gray J W; Pinkel D
Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors.
Genes, chromosomes & cancer 1994;10(4):231-43.
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1994: Kallioniemi A; Kallioniemi O P; Piper J; Tanner M; Stokke T; Chen L; Smith H S; Pinkel D; Gray J W; Waldman F M
Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(6):2156-60.
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1994: Kallioniemi O P; Kallioniemi A; Mascio L; Sudar D; Pinkel D; Deaven L; Gray J
Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis.
Genomics 1994;20(1):125-8.
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1994: Gray J W; Collins C; Henderson I C; Isola J; Kallioniemi A; Kallioniemi O P; Nakamura H; Pinkel D; Stokke T; Tanner M
Molecular cytogenetics of human breast cancer.
Cold Spring Harbor symposia on quantitative biology 1994;59():645-52.
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1993: Vooijs M; Yu L C; Tkachuk D; Pinkel D; Johnson D; Gray J W
Libraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR.
American journal of human genetics 1993;52(3):586-97.
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1993: Kallioniemi O P; Kallioniemi A; Sudar D; Rutovitz D; Gray J W; Waldman F; Pinkel D
Comparative genomic hybridization: a rapid new method for detecting and mapping DNA amplification in tumors.
Seminars in cancer biology 1993;4(1):41-6.
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1992: Gray J W; Kallioniemi A; Kallioniemi O; Pallavicini M; Waldman F; Pinkel D
Molecular cytogenetics: diagnosis and prognostic assessment.
Current opinion in biotechnology 1992;3(6):623-31.
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1992: Kallioniemi A; Kallioniemi O P; Sudar D; Rutovitz D; Gray J W; Waldman F; Pinkel D
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors.
Science (New York, N.Y.) 1992;258(5083):818-21.
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1992: Lucas J N; Awa A; Straume T; Poggensee M; Kodama Y; Nakano M; Ohtaki K; Weier H U; Pinkel D; Gray J
Rapid translocation frequency analysis in humans decades after exposure to ionizing radiation.
International journal of radiation biology 1992;62(1):53-63.
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1992: Kallioniemi O P; Kallioniemi A; Kurisu W; Thor A; Chen L C; Smith H S; Waldman F M; Pinkel D; Gray J W
ERBB2 amplification in breast cancer analyzed by fluorescence in situ hybridization.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(12):5321-5.
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1992: Matsumura K; Kallioniemi A; Kallioniemi O; Chen L; Smith H S; Pinkel D; Gray J; Waldman F M
Deletion of chromosome 17p loci in breast cancer cells detected by fluorescence in situ hybridization.
Cancer research 1992;52(12):3474-7.
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1992: Kallioniemi A; Kallioniemi O P; Waldman F M; Chen L C; Yu L C; Fung Y K; Smith H S; Pinkel D; Gray J W
Detection of retinoblastoma gene copy number in metaphase chromosomes and interphase nuclei by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1992;60(3-4):190-3.
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1991: Collins C; Kuo W L; Segraves R; Fuscoe J; Pinkel D; Gray J W
Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes.
Genomics 1991;11(4):997-1006.
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1991: Kuo W L; Tenjin H; Segraves R; Pinkel D; Golbus M S; Gray J
Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes.
American journal of human genetics 1991;49(1):112-9.
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1991: Weier H U; Lucas J N; Poggensee M; Segraves R; Pinkel D; Gray J W
Two-color hybridization with high complexity chromosome-specific probes and a degenerate alpha satellite probe DNA allows unambiguous discrimination between symmetrical and asymmetrical translocations.
Chromosoma 1991;100(6):371-6.
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1991: Brandriff B F; Gordon L A; Segraves R; Pinkel D
The male-derived genome after sperm-egg fusion: spatial distribution of chromosomal DNA and paternal-maternal genomic association.
Chromosoma 1991;100(4):262-6.
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1991: Tkachuk D C; Pinkel D; Kuo W L; Weier H U; Gray J W
Clinical applications of fluorescence in situ hybridization.
Genetic analysis, techniques and applications 1991;8(2):67-74.
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1991: Gray J W; Lucas J; Kallioniemi O; Kallioniemi A; Kuo W L; Straume T; Tkachuk D; Tenjin T; Weier H U; Pinkel D
Applications of fluorescence in situ hybridization in biological dosimetry and detection of disease-specific chromosome aberrations.
Progress in clinical and biological research 1991;372():399-411.
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1990: Wyrobek A J; Alhborn T; Balhorn R; Stanker L; Pinkel D
Fluorescence in situ hybridization to Y chromosomes in decondensed human sperm nuclei.
Molecular reproduction and development 1990;27(3):200-8.
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1990: Tkachuk D C; Westbrook C A; Andreeff M; Donlon T A; Cleary M L; Suryanarayan K; Homge M; Redner A; Gray J; Pinkel D
Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization.
Science (New York, N.Y.) 1990;250(4980):559-62.
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1990: Eastmond D A; Pinkel D
Detection of aneuploidy and aneuploidy-inducing agents in human lymphocytes using fluorescence in situ hybridization with chromosome-specific DNA probes.
Mutation research 1990;234(5):303-18.
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1990: Gray J W; Kuo W L; Liang J; Pinkel D; van den Engh G; Trask B; Tkachuk D; Waldman F; Westbrook C
Analytical approaches to detection and characterization of disease-linked chromosome aberrations.
Bone marrow transplantation 1990;6 Suppl 1():14-9.
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1990: Weier H U; Segraves R; Pinkel D; Gray J W
Synthesis of Y chromosome-specific labeled DNA probes by in vitro DNA amplification.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1990;38(3):421-6.
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1989: Trask B; Pinkel D; van den Engh G
The proximity of DNA sequences in interphase cell nuclei is correlated to genomic distance and permits ordering of cosmids spanning 250 kilobase pairs.
Genomics 1989;5(4):710-7.
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1989: van Dekken H; Pinkel D; Mullikin J; Trask B; van den Engh G; Gray J
Three-dimensional analysis of the organization of human chromosome domains in human and human-hamster hybrid interphase nuclei.
Journal of cell science 1989;94 ( Pt 2)():299-306.
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1989: Lucas J N; Tenjin T; Straume T; Pinkel D; Moore D; Litt M; Gray J W
Rapid human chromosome aberration analysis using fluorescence in situ hybridization.
International journal of radiation biology 1989;56(1):35-44.
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1989: Fuscoe J C; Collins C C; Pinkel D; Gray J W
An efficient method for selecting unique-sequence clones from DNA libraries and its application to fluorescent staining of human chromosome 21 using in situ hybridization.
Genomics 1989;5(1):100-9.
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1989: Eastmond D A; Pinkel D
Aneuploidy detection by analysis of interphase nuclei using fluorescence in situ hybridization with chromosome-specific probes.
Progress in clinical and biological research 1989;318():277-84.
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1989: van Dekken H; Pinkel D; Mullikin J; Trask B; van den Engh G; Gray J
Three dimensional reconstruction of human chromosomes in hybrid and human cell line nuclei using fluorescence in situ hybridization.
Acta histochemica. Supplementband 1989;37():91-4.
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1988: Pinkel D; Landegent J; Collins C; Fuscoe J; Segraves R; Lucas J; Gray J
Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(23):9138-42.
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1988: Trask B; van den Engh G; Pinkel D; Mullikin J; Waldman F; van Dekken H; Gray J
Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization.
Human genetics 1988;78(3):251-9.
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1988: van Dekken H; Pinkel D; Mullikin J; Gray J W
Enzymatic production of single-stranded DNA as a target for fluorescence in situ hybridization.
Chromosoma 1988;97(1):1-5.
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