CiteULike: pkonings's Hakonarson:H [7 articles]

Multiple testing in genome-wide association studies via hidden Markov models

Bioinformatics, Vol. 25, No. 21. (1 November 2009), pp. 2802-2808.

by Zhi Wei, Wenguang Sun, Kai Wang, Hakon Hakonarson

posted to multiple_testing hmm gwas by pkonings on 2009-08-17 09:08:20 as

along with 6 people and 1 group ppgardne djkt WJWilson rdiaz jmeppley guhjy Journal picks

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

Genome Research, Vol. 19, No. 9. (10 September 2009), pp. 1682-1690.

posted to cnv by pkonings on 2009-08-14 10:23:30 as

along with 7 people rdiaz ericrpaquet jandot guhjy frohike vplagnol daforerog

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Nature, Vol. 459, No. 7246. (28 May 2009), pp. 569-573.

by Joseph T. Glessner, Kai Wang, Guiqing Cai, et al.Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imielinski, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick M. Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James Flory, Frederick Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Geraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nurnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F. Grant, Maja Bucan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Hakon Hakonarson

posted to autism cnv by pkonings on 2009-06-15 14:28:00 as

along with 8 people rdiaz daforerog fenghezi scjparker dswan neils jbhiatt psique

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Nature, Vol. 459, No. 7246. (28 April 2009), pp. 528-533.

by Kai Wang, Haitao Zhang, Deqiong Ma, et al.Maja Bucan, Joseph T. Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P. Bradfield, Patrick M. A. Sleiman, Cecilia E. Kim, Cuiping Hou, Edward Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara M. Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. Mcmahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nurnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Geraldine Dawson, Struan F. A. Grant, Daniel H. Geschwind, Margaret A. Pericak-Vance, Gerard D. Schellenberg, Hakon Hakonarson

posted to autism gwas by pkonings on 2009-06-15 14:21:28 as

along with 6 people daforerog fenghezi scjparker jbhiatt psique wimufi

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy

Genome Research, Vol. advance access (13 January 2009)

by Edward F. Attiyeh, Sharon J. Diskin, Marc A. Attiyeh, et al.Yaël P. Mossé, Cuiping Hou, Eric M. Jackson, Cecilia Kim, Joseph Glessner, Hakon Hakonarson, Jaclyn A. Biegel, John M. Maris

posted to acgh cnv by pkonings on 2009-01-14 15:27:15 as

ATOM: a powerful gene-based association test by combining optimally weighted markers.

Bioinformatics (Oxford, England), Vol. 25, No. 4. (15 February 2009), pp. 497-503.

by M. Li, K. Wang, S. F. Grant, H. Hakonarson, C. Li

posted to gwas markers by pkonings on 2008-12-19 08:07:29 as

along with 4 people druvus djkt guhjy akmanning

SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation

Human Mutation, Vol. 9999, No. 9999. (2008), n/a.

by Binita M. Kamath, Brian D. Thiel, Xiaowu Gai, et al.Laura K. Conlin, Pedro S. Munoz, Joseph Glessner, Dinah Clark, Daniel M. Warthen, Tamim H. Shaikh, Ercan Mihci, David A. Piccoli, Struan F. A. Grant, Hakon Hakonarson, Ian D. Krantz, Nancy B. Spinner

posted to array cnv deletions snp by pkonings on 2008-12-08 13:38:42 as

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	Multiple testing in genome-wide association studies via hidden Markov models [My Copy] Bioinformatics, Vol. 25, No. 21. (1 November 2009), pp. 2802-2808. by Zhi Wei, Wenguang Sun, Kai Wang, Hakon Hakonarson posted to multiple_testing hmm gwas by pkonings on 2009-08-17 09:08:20 as along with 6 people and 1 group ppgardne djkt WJWilson rdiaz jmeppley guhjy Journal picks
	High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications [My Copy] Genome Research, Vol. 19, No. 9. (10 September 2009), pp. 1682-1690. by Tamim H. Shaikh, Xiaowu Gai, Juan C. Perin, et al.Joseph T. Glessner, Hongbo Xie, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K. Conlin, Monica D'Arcy, Edward C. Frackelton, Elizabeth A. Geiger, Chad Haldeman-Englert, Marcin Imielinski, Cecilia E. Kim, Livija Medne, Kiran Annaiah, Jonathan P. Bradfield, Elvira Dabaghyan, Andrew Eckert, Chioma C. Onyiah, Svetlana Ostapenko, F. George Otieno, Erin Santa, Julie L. Shaner, Robert Skraban, Ryan M. Smith, Josephine Elia, Elizabeth Goldmuntz, Nancy B. Spinner, Elaine H. Zackai, Rosetta M. Chiavacci, Robert Grundmeier, Eric F. Rappaport, Struan F. A. Grant, Peter S. White, Hakon Hakonarson posted to cnv by pkonings on 2009-08-14 10:23:30 as along with 7 people rdiaz ericrpaquet jandot guhjy frohike vplagnol daforerog
	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. [My Copy] Nature, Vol. 459, No. 7246. (28 May 2009), pp. 569-573. by Joseph T. Glessner, Kai Wang, Guiqing Cai, et al.Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imielinski, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick M. Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James Flory, Frederick Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana Michaels, Alexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Geraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nurnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F. Grant, Maja Bucan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Hakon Hakonarson posted to autism cnv by pkonings on 2009-06-15 14:28:00 as along with 8 people rdiaz daforerog fenghezi scjparker dswan neils jbhiatt psique
	Common genetic variants on 5p14.1 associate with autism spectrum disorders. [My Copy] Nature, Vol. 459, No. 7246. (28 April 2009), pp. 528-533. by Kai Wang, Haitao Zhang, Deqiong Ma, et al.Maja Bucan, Joseph T. Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P. Bradfield, Patrick M. A. Sleiman, Cecilia E. Kim, Cuiping Hou, Edward Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara M. Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. Mcmahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nurnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Geraldine Dawson, Struan F. A. Grant, Daniel H. Geschwind, Margaret A. Pericak-Vance, Gerard D. Schellenberg, Hakon Hakonarson posted to autism gwas by pkonings on 2009-06-15 14:21:28 as along with 6 people daforerog fenghezi scjparker jbhiatt psique wimufi
	Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy [My Copy] Genome Research, Vol. advance access (13 January 2009) by Edward F. Attiyeh, Sharon J. Diskin, Marc A. Attiyeh, et al.Yaël P. Mossé, Cuiping Hou, Eric M. Jackson, Cecilia Kim, Joseph Glessner, Hakon Hakonarson, Jaclyn A. Biegel, John M. Maris posted to acgh cnv by pkonings on 2009-01-14 15:27:15 as
	ATOM: a powerful gene-based association test by combining optimally weighted markers. [My Copy] Bioinformatics (Oxford, England), Vol. 25, No. 4. (15 February 2009), pp. 497-503. by M. Li, K. Wang, S. F. Grant, H. Hakonarson, C. Li posted to gwas markers by pkonings on 2008-12-19 08:07:29 as along with 4 people druvus djkt guhjy akmanning
	SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation [My Copy] Human Mutation, Vol. 9999, No. 9999. (2008), n/a. by Binita M. Kamath, Brian D. Thiel, Xiaowu Gai, et al.Laura K. Conlin, Pedro S. Munoz, Joseph Glessner, Dinah Clark, Daniel M. Warthen, Tamim H. Shaikh, Ercan Mihci, David A. Piccoli, Struan F. A. Grant, Hakon Hakonarson, Ian D. Krantz, Nancy B. Spinner posted to array cnv deletions snp by pkonings on 2008-12-08 13:38:42 as

pkonings's Hakonarson:H [7 articles] Export Sort

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