Results
|
1.
|
|
|
2.
|
|
|
3.
|
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans. [electronic resource] by
- Carlson, Jedidiah
- Locke, Adam E
- Flickinger, Matthew
- Zawistowski, Matthew
- Levy, Shawn
- Myers, Richard M
- Boehnke, Michael
- Kang, Hyun Min
- Scott, Laura J
- Li, Jun Z
- Zöllner, Sebastian
Producer: 20190114
In:
Nature communications vol. 9
Availability: No items available.
|
|
4.
|
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. [electronic resource] by
- Oliver, Tiffany Renee
- Tinker, Stuart W
- Allen, Emily Graves
- Hollis, Natasha
- Locke, Adam E
- Bean, Lora J H
- Chowdhury, Reshmi
- Begum, Ferdouse
- Marazita, Mary
- Cheung, Vivian
- Feingold, Eleanor
- Sherman, Stephanie L
Producer: 20120824
In:
Human genetics vol. 131
Availability: No items available.
|
|
5.
|
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. [electronic resource] by
- Ackerman, Christine
- Locke, Adam E
- Feingold, Eleanor
- Reshey, Benjamin
- Espana, Karina
- Thusberg, Janita
- Mooney, Sean
- Bean, Lora J H
- Dooley, Kenneth J
- Cua, Clifford L
- Reeves, Roger H
- Sherman, Stephanie L
- Maslen, Cheryl L
Producer: 20130317
In:
American journal of human genetics vol. 91
Availability: No items available.
|
|
6.
|
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project. [electronic resource] by
- Freeman, Sallie B
- Bean, Lora H
- Allen, Emily G
- Tinker, Stuart W
- Locke, Adam E
- Druschel, Charlotte
- Hobbs, Charlotte A
- Romitti, Paul A
- Royle, Marjorie H
- Torfs, Claudine P
- Dooley, Kenneth J
- Sherman, Stephanie L
Producer: 20080808
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 10
Availability: No items available.
|
|
7.
|
Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects. [electronic resource] by
- Ramachandran, Dhanya
- Mulle, Jennifer G
- Locke, Adam E
- Bean, Lora J H
- Rosser, Tracie C
- Bose, Promita
- Dooley, Kenneth J
- Cua, Clifford L
- Capone, George T
- Reeves, Roger H
- Maslen, Cheryl L
- Cutler, David J
- Sherman, Stephanie L
- Zwick, Michael E
Producer: 20160527
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 17
Availability: No items available.
|
|
8.
|
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project. [electronic resource] by
- Bean, Lora J H
- Allen, Emily G
- Tinker, Stuart W
- Hollis, Natasha D
- Locke, Adam E
- Druschel, Charlotte
- Hobbs, Charlotte A
- O'Leary, Leslie
- Romitti, Paul A
- Royle, Marjorie H
- Torfs, Claudine P
- Dooley, Kenneth J
- Freeman, Sallie B
- Sherman, Stephanie L
Producer: 20111222
In:
Birth defects research. Part A, Clinical and molecular teratology vol. 91
Availability: No items available.
|
|
9.
|
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. [electronic resource] by
- Ramachandran, Dhanya
- Zeng, Zhen
- Locke, Adam E
- Mulle, Jennifer G
- Bean, Lora J H
- Rosser, Tracie C
- Dooley, Kenneth J
- Cua, Clifford L
- Capone, George T
- Reeves, Roger H
- Maslen, Cheryl L
- Cutler, David J
- Feingold, Eleanor
- Sherman, Stephanie L
- Zwick, Michael E
Producer: 20160406
In:
G3 (Bethesda, Md.) vol. 5
Availability: No items available.
|
|
10.
|
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. [electronic resource] by
- Locke, Adam E
- Dooley, Kenneth J
- Tinker, Stuart W
- Cheong, Soo Yeon
- Feingold, Eleanor
- Allen, Emily G
- Freeman, Sallie B
- Torfs, Claudine P
- Cua, Clifford L
- Epstein, Michael P
- Wu, Michael C
- Lin, Xihong
- Capone, George
- Sherman, Stephanie L
- Bean, Lora J H
Producer: 20110114
In:
Genetic epidemiology vol. 34
Availability: No items available.
|
|
11.
|
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. [electronic resource] by
- Vrieze, Scott I
- Malone, Stephen M
- Vaidyanathan, Uma
- Kwong, Alan
- Kang, Hyun Min
- Zhan, Xiaowei
- Flickinger, Matthew
- Irons, Daniel
- Jun, Goo
- Locke, Adam E
- Pistis, Giorgio
- Porcu, Eleonora
- Levy, Shawn
- Myers, Richard M
- Oetting, William
- McGue, Matt
- Abecasis, Goncalo
- Iacono, William G
Producer: 20151012
In:
Psychophysiology vol. 51
Availability: No items available.
|
|
12.
|
Next-generation genotype imputation service and methods. [electronic resource] by
- Das, Sayantan
- Forer, Lukas
- Schönherr, Sebastian
- Sidore, Carlo
- Locke, Adam E
- Kwong, Alan
- Vrieze, Scott I
- Chew, Emily Y
- Levy, Shawn
- McGue, Matt
- Schlessinger, David
- Stambolian, Dwight
- Loh, Po-Ru
- Iacono, William G
- Swaroop, Anand
- Scott, Laura J
- Cucca, Francesco
- Kronenberg, Florian
- Boehnke, Michael
- Abecasis, Gonçalo R
- Fuchsberger, Christian
Producer: 20170623
In:
Nature genetics vol. 48
Availability: No items available.
|
|
13.
|
Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity. [electronic resource] by
- Hägg, Sara
- Ganna, Andrea
- Van Der Laan, Sander W
- Esko, Tonu
- Pers, Tune H
- Locke, Adam E
- Berndt, Sonja I
- Justice, Anne E
- Kahali, Bratati
- Siemelink, Marten A
- Pasterkamp, Gerard
- Strachan, David P
- Speliotes, Elizabeth K
- North, Kari E
- Loos, Ruth J F
- Hirschhorn, Joel N
- Pawitan, Yudi
- Ingelsson, Erik
Producer: 20160826
In:
Human molecular genetics vol. 24
Availability: No items available.
|
|
14.
|
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. [electronic resource] by
- Davis, James P
- Huyghe, Jeroen R
- Locke, Adam E
- Jackson, Anne U
- Sim, Xueling
- Stringham, Heather M
- Teslovich, Tanya M
- Welch, Ryan P
- Fuchsberger, Christian
- Narisu, Narisu
- Chines, Peter S
- Kangas, Antti J
- Soininen, Pasi
- Ala-Korpela, Mika
- Kuusisto, Johanna
- Collins, Francis S
- Laakso, Markku
- Boehnke, Michael
- Mohlke, Karen L
Producer: 20171117
In:
PLoS genetics vol. 13
Availability: No items available.
|
|
15.
|
Across-cohort QC analyses of GWAS summary statistics from complex traits. [electronic resource] by
- Chen, Guo-Bo
- Lee, Sang Hong
- Robinson, Matthew R
- Trzaskowski, Maciej
- Zhu, Zhi-Xiang
- Winkler, Thomas W
- Day, Felix R
- Croteau-Chonka, Damien C
- Wood, Andrew R
- Locke, Adam E
- Kutalik, Zoltán
- Loos, Ruth J F
- Frayling, Timothy M
- Hirschhorn, Joel N
- Yang, Jian
- Wray, Naomi R
- Visscher, Peter M
Producer: 20170726
In:
European journal of human genetics : EJHG vol. 25
Availability: No items available.
|
|
16.
|
Colocalization of GWAS and eQTL signals at loci with multiple signals identifies additional candidate genes for body fat distribution. [electronic resource] by
- Wu, Ying
- Broadaway, K Alaine
- Raulerson, Chelsea K
- Scott, Laura J
- Pan, Calvin
- Ko, Arthur
- He, Aiqing
- Tilford, Charles
- Fuchsberger, Christian
- Locke, Adam E
- Stringham, Heather M
- Jackson, Anne U
- Narisu, Narisu
- Kuusisto, Johanna
- Pajukanta, Päivi
- Collins, Francis S
- Boehnke, Michael
- Laakso, Markku
- Lusis, Aldons J
- Civelek, Mete
- Mohlke, Karen L
Producer: 20200623
In:
Human molecular genetics vol. 28
Availability: No items available.
|
|
17.
|
Quality control and conduct of genome-wide association meta-analyses. [electronic resource] by
- Winkler, Thomas W
- Day, Felix R
- Croteau-Chonka, Damien C
- Wood, Andrew R
- Locke, Adam E
- Mägi, Reedik
- Ferreira, Teresa
- Fall, Tove
- Graff, Mariaelisa
- Justice, Anne E
- Luan, Jian'an
- Gustafsson, Stefan
- Randall, Joshua C
- Vedantam, Sailaja
- Workalemahu, Tsegaselassie
- Kilpeläinen, Tuomas O
- Scherag, André
- Esko, Tonu
- Kutalik, Zoltán
- Heid, Iris M
- Loos, Ruth J F
Producer: 20141124
In:
Nature protocols vol. 9
Availability: No items available.
|
|
18.
|
Exome Sequencing of Familial Bipolar Disorder. [electronic resource] by
- Goes, Fernando S
- Pirooznia, Mehdi
- Parla, Jennifer S
- Kramer, Melissa
- Ghiban, Elena
- Mavruk, Senem
- Chen, Yun-Ching
- Monson, Eric T
- Willour, Virginia L
- Karchin, Rachel
- Flickinger, Matthew
- Locke, Adam E
- Levy, Shawn E
- Scott, Laura J
- Boehnke, Michael
- Stahl, Eli
- Moran, Jennifer L
- Hultman, Christina M
- Landén, Mikael
- Purcell, Shaun M
- Sklar, Pamela
- Zandi, Peter P
- McCombie, W Richard
- Potash, James B
Producer: 20170508
In:
JAMA psychiatry vol. 73
Availability: No items available.
|
|
19.
|
Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits. [electronic resource] by
- Raulerson, Chelsea K
- Ko, Arthur
- Kidd, John C
- Currin, Kevin W
- Brotman, Sarah M
- Cannon, Maren E
- Wu, Ying
- Spracklen, Cassandra N
- Jackson, Anne U
- Stringham, Heather M
- Welch, Ryan P
- Fuchsberger, Christian
- Locke, Adam E
- Narisu, Narisu
- Lusis, Aldons J
- Civelek, Mete
- Furey, Terrence S
- Kuusisto, Johanna
- Collins, Francis S
- Boehnke, Michael
- Scott, Laura J
- Lin, Dan-Yu
- Love, Michael I
- Laakso, Markku
- Pajukanta, Päivi
- Mohlke, Karen L
Producer: 20200402
In:
American journal of human genetics vol. 105
Availability: No items available.
|
|
20.
|
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. [electronic resource] by
- Teslovich, Tanya M
- Kim, Daniel Seung
- Yin, Xianyong
- Stancáková, Alena
- Jackson, Anne U
- Wielscher, Matthias
- Naj, Adam
- Perry, John R B
- Huyghe, Jeroen R
- Stringham, Heather M
- Davis, James P
- Raulerson, Chelsea K
- Welch, Ryan P
- Fuchsberger, Christian
- Locke, Adam E
- Sim, Xueling
- Chines, Peter S
- Narisu, Narisu
- Kangas, Antti J
- Soininen, Pasi
- Ala-Korpela, Mika
- Gudnason, Vilmundur
- Musani, Solomon K
- Jarvelin, Marjo-Riitta
- Schellenberg, Gerard D
- Speliotes, Elizabeth K
- Kuusisto, Johanna
- Collins, Francis S
- Boehnke, Michael
- Laakso, Markku
- Mohlke, Karen L
Producer: 20190211
In:
Human molecular genetics vol. 27
Availability: No items available.
|