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1
Runs of Homozygosity in European Populations
Runs of Homozygosity in European Populations
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Runs of Homozygosity in European Populations

McQuillan, Ruth ; Leutenegger, Anne-Louise ; Abdel-Rahman, Rehab ; Franklin, Christopher S. ; Pericic, Marijana ; Barac-Lauc, Lovorka ; Smolej-Narancic, Nina ; Janicijevic, Branka ; Polasek, Ozren ; Tenesa, Albert ; MacLeod, Andrew K. ; Farrington, Susan M. ; Rudan, Pavao ; Hayward, Caroline ; Vitart, Veronique ; Rudan, Igor ; Wild, Sarah H. ; Dunlop, Malcolm G. ; Wright, Alan F. ; Campbell, Harry ; Wilson, James F.

American journal of human genetics, 2008-09, Vol.83 (3), p.359-372 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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2
Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design
Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design
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Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design

Vitart, Veronique ; Carothers, Andrew D. ; Hayward, Caroline ; Teague, Peter ; Hastie, Nicholas D. ; Campbell, Harry ; Wright, Alan F.

American journal of human genetics, 2005-05, Vol.76 (5), p.763-772 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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3
Pitfalls in Homozygosity Mapping
Pitfalls in Homozygosity Mapping
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Pitfalls in Homozygosity Mapping

Miano, Maria G. ; Jacobson, Samuel G. ; Carothers, Andrew ; Hanson, Isabel ; Teague, Peter ; Lovell, Jill ; Cideciyan, Artur V. ; Haider, Neena ; Stone, Edwin M. ; Sheffield, Val C. ; Wright, Alan F.

American journal of human genetics, 2000-11, Vol.67 (5), p.1348-1351 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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4
Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis
Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis
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Discovery and Fine Mapping of Serum Protein Loci through Transethnic Meta-analysis

FRANCESCHINI, Nora ; VAN ROOIJ, Frank J. A ; BAUMERT, Jens ; BORASKA, Vesna ; BROER, Linda ; HAYWARD, Caroline ; NGWA, Julius S ; OKADA, Yukinori ; POLASEK, Ozren ; WESTRA, Harm-Jan ; WANG, Ying A ; DEL GRECO M, Fabiola ; PRINS, Bram P ; GLAZER, Nicole L ; KAPUR, Karen ; KEMA, Ido P ; LOPEZ, Lorna M ; SCHILLERT, Arne ; SMITH, Albert V ; WINKLER, Cheryl A ; ZGAGA, Lina ; BANDINELLI, Stefania ; BERGMANN, Sven ; FEITOSA, Mary F ; BOBAN, Mladen ; BOCHUD, Murielle ; CHEN, Y. D ; DAVIES, Gail ; DEHGHAN, Abbas ; JINGZHONG DING ; DOERING, Angela ; DURDA, J. Peter ; FERRUCCI, Luigi ; FRANCO, Oscar H ; KARAKAS, Mahir ; FRANKE, Lude ; GUNJACA, Grog ; HOFMAN, Albert ; HSU, Fang-Chi ; KOLCIC, Ivana ; KRAJA, Aldi ; KUBO, Michiaki ; LACKNER, Karl J ; LAUNER, Lenore ; LOEHR, Laura R ; ECKFELDT, John H ; GUO LI ; MEISINGER, Christa ; NAKAMURA, Yusuke ; SCHWIENBACHER, Christine ; STARR, John M ; TAKAHASHI, Atsushi ; TORLAK, Vesela ; UITTERLINDEN, Andre G ; VITART, Veronique ; WALDENBERGER, Melanie ; FOLSOM, Aaron R ; KOPP, Jeffrey ; VAEZ, Ahmad ; ANDREWS, Jeanette S

American journal of human genetics, 2012-10, Vol.91 (4), p.744-753 [Periódico revisado por pares]

Cambridge, MA: Cell Press

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5
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
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Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

Parry, David A. ; Brookes, Steven J. ; Logan, Clare V. ; Poulter, James A. ; El-Sayed, Walid ; Al-Bahlani, Suhaila ; Al Harasi, Sharifa ; Sayed, Jihad ; Raïf, El Mostafa ; Shore, Roger C. ; Dashash, Mayssoon ; Barron, Martin ; Morgan, Joanne E. ; Carr, Ian M. ; Taylor, Graham R. ; Johnson, Colin A. ; Aldred, Michael J. ; Dixon, Michael J. ; Wright, J. Tim ; Kirkham, Jennifer ; Inglehearn, Chris F. ; Mighell, Alan J.

American journal of human genetics, 2012-09, Vol.91 (3), p.565-571 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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6
Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
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Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

Medland, Sarah E. ; Nyholt, Dale R. ; Painter, Jodie N. ; McEvoy, Brian P. ; McRae, Allan F. ; Zhu, Gu ; Gordon, Scott D. ; Ferreira, Manuel A.R. ; Wright, Margaret J. ; Henders, Anjali K. ; Campbell, Megan J. ; Duffy, David L. ; Hansell, Narelle K. ; Macgregor, Stuart ; Slutske, Wendy S. ; Heath, Andrew C. ; Montgomery, Grant W. ; Martin, Nicholas G.

American journal of human genetics, 2009-11, Vol.85 (5), p.750-755 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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7
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
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Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

Lange, Leslie A. ; Schmidt, Ellen M. ; Bizon, Chris ; Jun, Goo ; Auer, Paul ; Li, Kuo-ping ; Locke, Adam ; Rivas, Manuel A. ; Feitosa, Mary F. ; Zhang, Qunyuan ; Huffman, Jennifer E. ; Crosby, Jacy ; Robinson, Jennifer G. ; Crosslin, David R. ; Rosenthal, Elisabeth A. ; Tsai, Michael ; Rieder, Mark J. ; Fox, Ervin R. ; van Duijn, Cornelia M. ; Taylor, Herman A. ; Loos, Ruth J.F. ; Ballantyne, Christie M. ; Reiner, Alexander P. ; Cupples, L. Adrienne ; Kang, Hyun Min ; Lettre, Guillaume ; Rader, Daniel J. ; Reilly, Muredach P. ; Stoletzki, Nina ; Barr, R. Graham ; Benjamin, Emelia J. ; Carr, Jeff ; Dupuis, Josée ; Ellis, Jaclyn ; Fornage, Myriam ; Goff, David ; Grody, Wayne ; Heard-Costa, Nancy L. ; Levy, Daniel ; Li, Dalin ; Loria, Cay ; Mackey, Rachel ; Quinlan, Aaron R. ; Rice, Kenneth ; Sanders, Jill P. ; Tracy, Russell P. ; Tsai, Michael Y. ; Wassel, Chrstina L. ; Watson, Karol ; Wilson, Gregory ; Wilson, James G. ; Zakai, Neil A. ; Nalls, Michael ; Bamshad, Michael J. ; Accurso, Frank ; Beaty, Terri ; Caplan, Daniel ; Chidekel, Aaron ; Christiani, David C. ; De Paula, Alicia ; Gutierrez, Hector ; Hassoun, Paul M. ; Hiatt, Peter ; Hummer, Laura K. ; Kim, Yoonhee ; Lin, Xihong ; Louie, Tin L. ; Mathias, Rasika A. ; McNamara, John ; McNamara, Sharon ; Nielson, Dennis ; Orenstein, David ; O’Sullivan, Brian ; Passero, Mary Ann ; Perkett, Elizabeth ; Spencer, Terry ; Tabor, Holly K. ; Weiss, Robert ; Wigley, Fred ; Wise, Robert A. ; Wurfel, Mark M. ; Eichler, Evan E. ; Fu, Wenqing ; Smith, Joshua D. ; Tennessen, Jacob A. ; Peters, Ulrike ; Brzyski, Robert ; Curb, J. David ; Eaton, Charles B. ; Heiss, Gerardo ; Johnson, Karen C. ; Lasser, Norman ; Lin, Dan-Yu ; Logsdon, Benjamin A. ; Manson, JoAnn E. ; Martin, Lisa ; Stein, Evan ; Applebaum-Bowden, Deborah ; Paltoo, Dina N. ; Sturcke, Anne

American journal of human genetics, 2014-02, Vol.94 (2), p.233-245 [Periódico revisado por pares]

United States: Elsevier Inc

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