Article: Human chromosome 7: DNA sequence and biology
| Title | Human chromosome 7: DNA sequence and biology |
|---|---|
| Authors | Scherer, SW28 34 Cheung, J34 MacDonald, JR34 Osborne, LR28 Nakabayashi, K34 Herbrick, JA34 Carson, AR34 ParkerKatiraee, L28 34 Skaug, J34 Khaja, R34 Zhang, J34 Hudek, AK34 Li, M34 Haddad, M34 Duggan, GE34 Fernandez, BA2 Kanematsu, E34 Gentles, S34 Christopoulos, CC34 Choufani, S34 Kwasnicka, D34 Zheng, XH11 Lai, Z11 Nusskern, D11 Zhang, Q11 Gu, Z11 Lu, F11 Zeesman, S6 Nowaczyk, MJ6 Teshima, I28 34 Chitayat, D28 34 Shuman, C28 34 Weksberg, R28 34 Zackai, EH7 Grebe, TA9 Cox, SR9 Kirkpatrick, SJ14 Rahman, N15 Friedman, JM24 Heng, HHQ19 Pelicci, PG21 26 LoCoco, F12 Belloni, E21 26 Shaffer, LG3 Pober, B23 Morton, CC10 31 Gusella, JF1 Bruns, GAP33 Korf, BR10 31 Quade, BJ31 Ligon, AH31 Ferguson, H31 Higgins, AW31 Leach, NT31 Herrick, SR31 Lemyre, E31 Farra, CG31 Kim, HG1 Summers, AM32 Gripp, KW5 Roberts, W34 Szatmari, P6 Winsor, EJT17 Grzeschik, KH20 Teebi, A28 34 Minassian, BA34 Kere, J4 Armengol, L8 Pujana, MA8 Estivill, X8 Wilson, MD22 Koop, BF22 Tosi, S25 Moore, GE18 Boright, AP17 Zlotorynski, E27 Kerem, B27 Kroisel, PM16 Petek, E16 Oscier, DG30 Mould, SJ30 Döhner, H29 Döhner, K29 Rommens, JM28 34 Vincent, JB28 Venter, JC11 Li, PW11 Mural, RJ11 Adams, MD11 Tsui, LC13 28 34 |
| Issue Date | 2003 |
| Publisher | American Association for the Advancement of Science. The Journal's web site is located at http://sciencemag.org |
| Citation | Science, 2003, v. 300 n. 5620, p. 767-772 [How to Cite?] DOI: http://dx.doi.org/10.1126/science.1083423 |
| Abstract | DNA sequence and annotation of the entire human chromosome 7, encompassing nearly 158 million nucleotides of DNA and 1917 gene structures, are presented. To generate a higher order description, additional structural features such as imprinted genes, fragile sites, and segmental duplications were integrated at the level of the DNA sequence with medical genetic data, including 440 chromosome rearrangement breakpoints associated with disease. This approach enabled the discovery of candidate genes for developmental diseases including autism. |
| ISSN | 0036-8075 2011 Impact Factor: 31.201 2011 SCImago Journal Rankings: 5.425 |
| DOI | http://dx.doi.org/10.1126/science.1083423 |
| PubMed Central ID | PMC2882961 |
| References | References in Scopus |
| dc.contributor.author | Scherer, SW |
|---|---|
| dc.contributor.author | Cheung, J |
| dc.contributor.author | MacDonald, JR |
| dc.contributor.author | Osborne, LR |
| dc.contributor.author | Nakabayashi, K |
| dc.contributor.author | Herbrick, JA |
| dc.contributor.author | Carson, AR |
| dc.contributor.author | ParkerKatiraee, L |
| dc.contributor.author | Skaug, J |
| dc.contributor.author | Khaja, R |
| dc.contributor.author | Zhang, J |
| dc.contributor.author | Hudek, AK |
| dc.contributor.author | Li, M |
| dc.contributor.author | Haddad, M |
| dc.contributor.author | Duggan, GE |
| dc.contributor.author | Fernandez, BA |
| dc.contributor.author | Kanematsu, E |
| dc.contributor.author | Gentles, S |
| dc.contributor.author | Christopoulos, CC |
| dc.contributor.author | Choufani, S |
| dc.contributor.author | Kwasnicka, D |
| dc.contributor.author | Zheng, XH |
| dc.contributor.author | Lai, Z |
| dc.contributor.author | Nusskern, D |
| dc.contributor.author | Zhang, Q |
| dc.contributor.author | Gu, Z |
| dc.contributor.author | Lu, F |
| dc.contributor.author | Zeesman, S |
| dc.contributor.author | Nowaczyk, MJ |
| dc.contributor.author | Teshima, I |
| dc.contributor.author | Chitayat, D |
| dc.contributor.author | Shuman, C |
| dc.contributor.author | Weksberg, R |
| dc.contributor.author | Zackai, EH |
| dc.contributor.author | Grebe, TA |
| dc.contributor.author | Cox, SR |
| dc.contributor.author | Kirkpatrick, SJ |
| dc.contributor.author | Rahman, N |
| dc.contributor.author | Friedman, JM |
| dc.contributor.author | Heng, HHQ |
| dc.contributor.author | Pelicci, PG |
| dc.contributor.author | LoCoco, F |
| dc.contributor.author | Belloni, E |
| dc.contributor.author | Shaffer, LG |
| dc.contributor.author | Pober, B |
| dc.contributor.author | Morton, CC |
| dc.contributor.author | Gusella, JF |
| dc.contributor.author | Bruns, GAP |
| dc.contributor.author | Korf, BR |
| dc.contributor.author | Quade, BJ |
| dc.contributor.author | Ligon, AH |
| dc.contributor.author | Ferguson, H |
| dc.contributor.author | Higgins, AW |
| dc.contributor.author | Leach, NT |
| dc.contributor.author | Herrick, SR |
| dc.contributor.author | Lemyre, E |
| dc.contributor.author | Farra, CG |
| dc.contributor.author | Kim, HG |
| dc.contributor.author | Summers, AM |
| dc.contributor.author | Gripp, KW |
| dc.contributor.author | Roberts, W |
| dc.contributor.author | Szatmari, P |
| dc.contributor.author | Winsor, EJT |
| dc.contributor.author | Grzeschik, KH |
| dc.contributor.author | Teebi, A |
| dc.contributor.author | Minassian, BA |
| dc.contributor.author | Kere, J |
| dc.contributor.author | Armengol, L |
| dc.contributor.author | Pujana, MA |
| dc.contributor.author | Estivill, X |
| dc.contributor.author | Wilson, MD |
| dc.contributor.author | Koop, BF |
| dc.contributor.author | Tosi, S |
| dc.contributor.author | Moore, GE |
| dc.contributor.author | Boright, AP |
| dc.contributor.author | Zlotorynski, E |
| dc.contributor.author | Kerem, B |
| dc.contributor.author | Kroisel, PM |
| dc.contributor.author | Petek, E |
| dc.contributor.author | Oscier, DG |
| dc.contributor.author | Mould, SJ |
| dc.contributor.author | Döhner, H |
| dc.contributor.author | Döhner, K |
| dc.contributor.author | Rommens, JM |
| dc.contributor.author | Vincent, JB |
| dc.contributor.author | Venter, JC |
| dc.contributor.author | Li, PW |
| dc.contributor.author | Mural, RJ |
| dc.contributor.author | Adams, MD |
| dc.contributor.author | Tsui, LC |
| dc.date.accessioned | 2007-09-12T03:52:27Z |
| dc.date.available | 2007-09-12T03:52:27Z |
| dc.date.issued | 2003 |
| dc.description.abstract | DNA sequence and annotation of the entire human chromosome 7, encompassing nearly 158 million nucleotides of DNA and 1917 gene structures, are presented. To generate a higher order description, additional structural features such as imprinted genes, fragile sites, and segmental duplications were integrated at the level of the DNA sequence with medical genetic data, including 440 chromosome rearrangement breakpoints associated with disease. This approach enabled the discovery of candidate genes for developmental diseases including autism. |
| dc.description.nature | link_to_OA_fulltext |
| dc.identifier.citation | Science, 2003, v. 300 n. 5620, p. 767-772 [How to Cite?] DOI: http://dx.doi.org/10.1126/science.1083423 |
| dc.identifier.doi | http://dx.doi.org/10.1126/science.1083423 |
| dc.identifier.epage | 772 |
| dc.identifier.isi | WOS:000182579800041 |
| dc.identifier.issn | 0036-8075 2011 Impact Factor: 31.201 2011 SCImago Journal Rankings: 5.425 |
| dc.identifier.issue | 5620 |
| dc.identifier.openurl | ![]() |
| dc.identifier.pmcid | PMC2882961 |
| dc.identifier.pmid | 12690205 |
| dc.identifier.scopus | eid_2-s2.0-0038756128 |
| dc.identifier.spage | 767 |
| dc.identifier.uri | http://hdl.handle.net/10722/44382 |
| dc.identifier.volume | 300 |
| dc.language | eng |
| dc.publisher | American Association for the Advancement of Science. The Journal's web site is located at http://sciencemag.org |
| dc.publisher.place | United States |
| dc.relation.ispartof | Science |
| dc.relation.references | References in Scopus |
| dc.rights | Science. Copyright © American Association for the Advancement of Science. |
| dc.subject.mesh | Chromosomes, human, pair 7 - genetics |
| dc.subject.mesh | Sequence analysis, dna |
| dc.subject.mesh | Genetic diseases, inborn - genetics |
| dc.subject.mesh | Dna, complementary |
| dc.subject.mesh | Expressed sequence tags |
| dc.title | Human chromosome 7: DNA sequence and biology |
| dc.type | Article |
Author Affiliations
- Massachusetts General Hospital
- Memorial University of Newfoundland, Faculty of Medicine
- Baylor College of Medicine
- Karolinska University Hospital
- Alfred I. duPont Hospital for Children
- McMaster University
- The Children's Hospital of Philadelphia
- Centro de Regulacion Genomica
- University of Phoenix
- Harvard Medical School
- Celera Rockville
- Università degli Studi di Roma Tor Vergata
- The University of Hong Kong
- University of Wisconsin Madison
- Section of Cancer Genetics
- Karl-Franzens-Universitat Graz
- University Health Network
- Imperial College London
- Wayne State University School of Medicine
- Universität Marburg
- Fondazione IFOM Istituto Firc di Oncologia Molecolare
- University of Victoria
- Yale University School of Medicine
- The University of British Columbia
- John Radcliffe Hospital
- Istituto Europeo di Oncologia
- Hebrew University of Jerusalem
- University of Toronto
- Universitätsklinikum Ulm
- Royal Bournemouth Hospital
- Brigham and Women's Hospital
- North York General Hospital
- Children's Hospital Boston
- Hospital for Sick Children, Toronto


