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Peter White
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Research Profile (preview)
Anatomy
Disorders
Procedures
Genes & Molecular Sequences
Chemicals & Drugs
Living Beings
Concepts & Ideas
Physiology
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Network (preview)
35
Brodeur, Garrett
30
Maris, John
22
Sulman, Erik
16
Hogarty, Michael
12
Guo, Chun
11
Biegel, Jaclyn
10
Thompson, Patricia
9
Jensen, SJ
8
Allen, C
7
Matise, Tara
6
Seeger, Robert
6
Gerbing, Robert
5
Weiss, Mitchell
4
Stram, DO
4
Gregory, Simon
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Publications
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Geonetwork of Peter White (preview)
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All Publications
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2008: Fujita Tomoyuki; Igarashi Jun; Okawa Erin R; Gotoh Takahiro; Manne Jayanthi; Kolla Venkatadri; Kim Jessica; Zhao Huaqing; Pawel Bruce R; London Wendy B; Maris John M; White Peter S; Brodeur Garrett M
CHD5, a tumor suppressor gene deleted from 1p36.31 in neuroblastomas.
Journal of the National Cancer Institute 2008;100(13):940-9.
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2008: Weiss Jayne S; Kruth Howard S; Kuivaniemi Helena; Tromp Gerard; Karkera Jayaprakash; Mahurkar Sunil; Lisch Walter; Dupps William J; White Peter S; Winters R Scott; Kim Chaesik; Rapuano Christopher J; Sutphin John; Reidy Jim; Hu Fung-Rong; Lu Da Wen; Ebenezer Neil; Nickerson Michael L
Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function.
American journal of medical genetics. Part A 2008;146(3):271-83.
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2008: Okawa E R; Gotoh T; Manne J; Igarashi J; Fujita T; Silverman K A; Xhao H; Mosse Y P; White P S; Brodeur G M
Expression and sequence analysis of candidates for the 1p36.31 tumor suppressor gene deleted in neuroblastomas.
Oncogene 2008;27(6):803-10.
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2007: Weiss Jayne S; Kruth Howard S; Kuivaniemi Helena; Tromp Gerard; White Peter S; Winters R Scott; Lisch Walter; Henn Wolfram; Denninger Elke; Krause Matthias; Wasson Paul; Ebenezer Neil; Mahurkar Sunil; Nickerson Michael L
Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy.
Investigative ophthalmology & visual science 2007;48(11):5007-12.
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2006: McDonald Ryan; Scott Winters R; Ankuda Claire K; Murphy Joan A; Rogers Amy E; Pereira Fernando; Greenblatt Marc S; White Peter S
An automated procedure to identify biomedical articles that contain cancer-associated gene variants.
Human mutation 2006;27(9):957-64.
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2006: Jin Yang; McDonald Ryan T; Lerman Kevin; Mandel Mark A; Carroll Steven; Liberman Mark Y; Pereira Fernando C; Winters Raymond S; White Peter S
Automated recognition of malignancy mentions in biomedical literature.
BMC bioinformatics 2006;7():492.
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2005: Maris John M; Hii George; Gelfand Craig A; Varde Shobha; White Peter S; Rappaport Eric; Surrey Saul; Fortina Paolo
Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform.
Genome research 2005;15(8):1168-76.
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2005: White Peter S; Thompson Patricia M; Gotoh Takahiro; Okawa Erin R; Igarashi Jun; Kok Marleen; Winter Cynthia; Gregory Simon G; Hogarty Michael D; Maris John M; Brodeur Garrett M
Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma.
Oncogene 2005;24(16):2684-94.
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2005: Scavello Genaro S; Paluru Prasuna C; Zhou Jie; White Peter S; Rappaport Eric F; Young Terri L
Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes.
Molecular vision 2005;11():97-110.
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2004: Kong X; Murphy K; Raj T; He C; White P S; Matise T C
A combined linkage-physical map of the human genome.
American journal of human genetics 2004;75(6):1143-8.
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2004: McDonald Ryan T; Winters R Scott; Mandel Mark; Jin Yang; White Peter S; Pereira Fernando
An entity tagger for recognizing acquired genomic variations in cancer literature.
Bioinformatics (Oxford, England) 2004;20(17):3249-51.
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2004: Theendakara Veena; Tromp Gerard; Kuivaniemi Helena; White Peter S; Panchal Seema; Cox Jennifer; Winters R Scott; Riebeling Petra; Tost Frank; Hoeltzenbein Maria; Tervo Timo M; Henn Wolfram; Denniger Elke; Krause Matthias; Koksal Murat; Kargi Sebnem; Ugurbas Suat H; Latvala Terho; Shearman Amanda M; Weiss Jayne S
Fine mapping of the Schnyder's crystalline corneal dystrophy locus.
Human genetics 2004;114(6):594-600.
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2004: Murphy Kevin; Raj Towfique; Winters R Scott; White Peter S
me-PCR: a refined ultrafast algorithm for identifying sequence-defined genomic elements.
Bioinformatics (Oxford, England) 2004;20(4):588-90.
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2004: Sulman Erik P; White Peter S; Brodeur Garrett M
Genomic annotation of the meningioma tumor suppressor locus on chromosome 1p34.
Oncogene 2004;23(4):1014-20.
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2003: Thompson Patricia M; Gotoh Takahiro; Kok Marleen; White Peter S; Brodeur Garrett M
CHD5, a new member of the chromodomain gene family, is preferentially expressed in the nervous system.
Oncogene 2003;22(7):1002-11.
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2002: Maris John M; Weiss Matthew J; Mosse Yael; Hii George; Guo Chun; White Peter S; Hogarty Michael D; Mirensky Tamar; Brodeur Garrett M; Rebbeck Timothy R; Urbanek Margrit; Shusterman Suzanne
Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.
Cancer research 2002;62(22):6651-8.
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2002: Hogarty Michael D; Winter Cynthia L; Liu Xueyuan; Guo Chun; White Peter S; Look A Thomas; Brodeur Garrett M; Maris John M
No evidence for the presence of an imprinted neuroblastoma suppressor gene within chromosome sub-band 1p36.3.
Cancer research 2002;62(22):6481-4.
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2002: Matise Tara C; Porter Christopher J; Buyske Steven; Cuttichia A Jamie; Sulman Erik P; White Peter S
Systematic evaluation of map quality: human chromosome 22.
American journal of human genetics 2002;70(6):1398-410.
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2001: Wang Z G; White P S; Ackerman S H
Atp11p and Atp12p are assembly factors for the F(1)-ATPase in human mitochondria.
The Journal of biological chemistry 2001;276(33):30773-8.
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2001: Hogarty M D; Maris J M; White P S; Guo C; Brodeur G M
Analysis of genomic imprinting at 1p35-36 in neuroblastoma.
Medical and pediatric oncology 2001;36(1):52-5.
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2001: White P S; Thompson P M; Seifried B A; Sulman E P; Jensen S J; Guo C; Maris J M; Hogarty M D; Allen C; Biegel J A; Matise T C; Gregory S G; Reynolds C P; Brodeur G M
Detailed molecular analysis of 1p36 in neuroblastoma.
Medical and pediatric oncology 2001;36(1):37-41.
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2001: Maris J M; Guo C; Blake D; White P S; Hogarty M D; Thompson P M; Rajalingam V; Gerbing R; Stram D O; Matthay K K; Seeger R C; Brodeur G M
Comprehensive analysis of chromosome 1p deletions in neuroblastoma.
Medical and pediatric oncology 2001;36(1):32-6.
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2001: Thompson P M; Seifried B A; Kyemba S K; Jensen S J; Guo C; Maris J M; Brodeur G M; Stram D O; Seeger R C; Gerbing R; Matthay K K; Matise T C; White P S
Loss of heterozygosity for chromosome 14q in neuroblastoma.
Medical and pediatric oncology 2001;36(1):28-31.
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2001: Maris J M; Guo C; White P S; Hogarty M D; Thompson P M; Stram D O; Gerbing R; Matthay K K; Seeger R C; Brodeur G M
Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma.
Medical and pediatric oncology 2001;36(1):24-7.
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2001: Thompson P M; Maris J M; Hogarty M D; Seeger R C; Reynolds C P; Brodeur G M; White P S
Homozygous deletion of CDKN2A (p16INK4a/p14ARF) but not within 1p36 or at other tumor suppressor loci in neuroblastoma.
Cancer research 2001;61(2):679-86.
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2001: White P S; Matise T C
Genomic mapping and mapping databases.
Methods of biochemical analysis 2001;43():111-53.
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2001: Schutte B C; Carpten J D; Forus A; Gregory S G; Horii A; White P S
Report and abstracts of the sixth international workshop on human chromosome 1 mapping 2000. Iowa City, Iowa, USA. 30 September-3 October 2000.
Cytogenetics and cell genetics 2001;92(1-2):23-41.
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2000: Hogarty M D; Liu X; Thompson P M; White P S; Sulman E P; Maris J M; Brodeur G M
BIN1 inhibits colony formation and induces apoptosis in neuroblastoma cell lines with MYCN amplification.
Medical and pediatric oncology 2000;35(6):559-62.
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2000: Guo C; White P S; Hogarty M D; Brodeur G M; Gerbing R; Stram D O; Maris J M
Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas.
Medical and pediatric oncology 2000;35(6):544-6.
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2000: Weiss M J; Guo C; Shusterman S; Hii G; Mirensky T L; White P S; Hogarty M D; Rebbeck T R; Teare D; Urbanek M; Brodeur G M; Maris J M
Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13.
Medical and pediatric oncology 2000;35(6):526-30.
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2000: Hogarty M D; Liu X; Guo C; Thompson P M; Weiss M J; White P S; Sulman E P; Brodeur G M; Maris J M
Identification of a 1-megabase consensus region of deletion at 1p36.3 in primary neuroblastomas.
Medical and pediatric oncology 2000;35(6):512-5.
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2000: Nicole S; Davoine C S; Topaloglu H; Cattolico L; Barral D; Beighton P; Hamida C B; Hammouda H; Cruaud C; White P S; Samson D; Urtizberea J A; Lehmann-Horn F; Weissenbach J; Hentati F; Fontaine B
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).
Nature genetics 2000;26(4):480-3.
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2000: Frühwald M C; O'Dorisio M S; Rush L J; Reiter J L; Smiraglia D J; Wenger G; Costello J F; White P S; Krahe R; Brodeur G M; Plass C
Gene amplification in PNETs/medulloblastomas: mapping of a novel amplified gene within the MYCN amplicon.
Journal of medical genetics 2000;37(7):501-9.
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2000: Maris J M; Weiss M J; Guo C; Gerbing R B; Stram D O; White P S; Hogarty M D; Sulman E P; Thompson P M; Lukens J N; Matthay K K; Seeger R C; Brodeur G M
Loss of heterozygosity at 1p36 independently predicts for disease progression but not decreased overall survival probability in neuroblastoma patients: a Children's Cancer Group study.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2000;18(9):1888-99.
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1999: White P S; Sulman E P; Porter C J; Matise T C
A comprehensive view of human chromosome 1.
Genome research 1999;9(10):978-88.
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1999: Guo C; White P S; Weiss M J; Hogarty M D; Thompson P M; Stram D O; Gerbing R; Matthay K K; Seeger R C; Brodeur G M; Maris J M
Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas.
Oncogene 1999;18(35):4948-57.
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1999: Nicole S; White P S; Topaloglu H; Beigthon P; Salih M; Hentati F; Fontaine B
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene.
Human genetics 1999;105(1-2):98-103.
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1999: White P S; Forus A; Matise T C; Schutte B C; Spieker N; Stanier P; Vance J M; Gregory S G
Report of the fifth international workshop on human chromosome 1 mapping 1999.
Cytogenetics and cell genetics 1999;87(3-4):143-71.
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1998: Hogarty M D; White P S; Sulman E P; Brodeur G M
Mononucleotide repeat instability is infrequent in neuroblastoma.
Cancer genetics and cytogenetics 1998;106(2):140-3.
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1998: Sulman E P; Dumanski J P; White P S; Zhao H; Maris J M; Mathiesen T; Bruder C; Cnaan A; Brodeur G M
Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity.
Cancer research 1998;58(15):3226-30.
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1998: White P S; Jensen S J; Rajalingam V; Stairs D; Sulman E P; Maris J M; Biegel J A; Wooster R; Brodeur G M
Physical mapping of the CA6, ENO1, and SLC2A5 (GLUT5) genes and reassignment of SLC2A5 to 1p36.2.
Cytogenetics and cell genetics 1998;81(1):60-4.
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1997: Maris J M; Jensen J; Sulman E P; Beltinger C P; Allen C; Biegel J A; Brodeur G M; White P S
Human Krüppel-related 3 (HKR3): a candidate for the 1p36 neuroblastoma tumour suppressor gene?
European journal of cancer (Oxford, England : 1990) 1997;33(12):1991-6.
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1997: White P S; Maris J M; Sulman E P; Jensen S J; Kyemba S M; Beltinger C P; Allen C; Kramer D L; Biegel J A; Brodeur G M
Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma.
European journal of cancer (Oxford, England : 1990) 1997;33(12):1957-61.
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1997: Maris J M; Kyemba S M; Rebbeck T R; White P S; Sulman E P; Jensen S J; Allen C; Biegel J A; Brodeur G M
Molecular genetic analysis of familial neuroblastoma.
European journal of cancer (Oxford, England : 1990) 1997;33(12):1923-8.
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1997: Jensen S J; Sulman E P; Maris J M; Matise T C; Vojta P J; Barrett J C; Brodeur G M; White P S
An integrated transcript map of human chromosome 1p35-p36.
Genomics 1997;42(1):126-36.
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1997: Reddy U R; Phatak S; Allen C; Nycum L M; Sulman E P; White P S; Biegel J A
Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis.
Genomics 1997;41(2):283-5.
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1997: Brodeur G M; Maris J M; Yamashiro D J; Hogarty M D; White P S
Biology and genetics of human neuroblastomas.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 1997;19(2):93-101.
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1996: Kuroda H; White P S; Sulman E P; Manohar C F; Reiter J L; Cohn S L; Brodeur G M
Physical mapping of the DDX1 gene to 340 kb 5' of MYCN.
Oncogene 1996;13(7):1561-5.
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1996: Maris J M; Kyemba S M; Rebbeck T R; White P S; Sulman E P; Jensen S J; Allen C; Biegel J A; Yanofsky R A; Feldman G L; Brodeur G M
Familial predisposition to neuroblastoma does not map to chromosome band 1p36.
Cancer research 1996;56(15):3421-5.
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1996: Maris J M; Jensen S J; Sulman E P; Beltinger C P; Gates K; Allen C; Biegel J A; Brodeur G M; White P S
Cloning, chromosomal localization, physical mapping, and genomic characterization of HKR3.
Genomics 1996;35(2):289-98.
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1996: Beltinger C P; White P S; Maris J M; Sulman E P; Jensen S J; LePaslier D; Stallard B J; Goeddel D V; de Sauvage F J; Brodeur G M
Physical mapping and genomic structure of the human TNFR2 gene.
Genomics 1996;35(1):94-100.
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1995: Maris J M; White P S; Beltinger C P; Sulman E P; Castleberry R P; Shuster J J; Look A T; Brodeur G M
Significance of chromosome 1p loss of heterozygosity in neuroblastoma.
Cancer research 1995;55(20):4664-9.
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1995: White P S; Maris J M; Beltinger C; Sulman E; Marshall H N; Fujimori M; Kaufman B A; Biegel J A; Allen C; Hilliard C
A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(12):5520-4.
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1995: Beltinger C P; White P S; Sulman E P; Maris J M; Brodeur G M
No CDKN2 mutations in neuroblastomas.
Cancer research 1995;55(10):2053-5.
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1995: Nakagawara A; Liu X G; Ikegaki N; White P S; Yamashiro D J; Nycum L M; Biegel J A; Brodeur G M
Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2).
Genomics 1995;25(2):538-46.
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1993: Biegel J A; White P S; Marshall H N; Fujimori M; Zackai E H; Scher C D; Brodeur G M; Emanuel B S
Constitutional 1p36 deletion in a child with neuroblastoma.
American journal of human genetics 1993;52(1):176-82.
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