Results
|
|
61.
|
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. [electronic resource] by
- Ogdie, Matthew N
- Fisher, Simon E
- Yang, May
- Ishii, Janeen
- Francks, Clyde
- Loo, Sandra K
- Cantor, Rita M
- McCracken, James T
- McGough, James J
- Smalley, Susan L
- Nelson, Stanley F
Producer: 20041216
In:
American journal of human genetics vol. 75
Availability: No items available.
|
|
|
62.
|
Identifying heritable brain phenotypes in an extended pedigree of vervet monkeys. [electronic resource] by
- Fears, Scott C
- Melega, William P
- Service, Susan K
- Lee, Chris
- Chen, Kelly
- Tu, Zhuowen
- Jorgensen, Matthew J
- Fairbanks, Lynn A
- Cantor, Rita M
- Freimer, Nelson B
- Woods, Roger P
Producer: 20090410
In:
The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 29
Availability: No items available.
|
|
|
63.
|
Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia. [electronic resource] by
- Allayee, Hooman
- Krass, Kelly L
- Pajukanta, Päivi
- Cantor, Rita M
- van der Kallen, Carla J H
- Mar, Rebecca
- Rotter, Jerome I
- de Bruin, Tjerk W A
- Peltonen, Leena
- Lusis, Aldons J
Producer: 20020514
In:
Circulation research vol. 90
Availability: No items available.
|
|
|
64.
|
GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics. [electronic resource] by
- Tintle, Nathan L
- Fardo, David W
- de Andrade, Mariza
- Aslibekyan, Stella
- Bailey, Julia N
- Bermejo, Justo Lorenzo
- Cantor, Rita M
- Ghosh, Saurabh
- Melton, Philip
- Wang, Xuexia
- MacCluer, Jean W
- Almasy, Laura
Publication details: BMC proceedings 2018
In:
BMC proceedings vol. 12
Availability: No items available.
|
|
|
65.
|
Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia. [electronic resource] by
- Mar-Heyming, Rebecca
- Miyazaki, Makoto
- Weissglas-Volkov, Daphna
- Kolaitis, Nicholas A
- Sadaat, Narimaan
- Plaisier, Christopher
- Pajukanta, Päivi
- Cantor, Rita M
- de Bruin, Tjerk W A
- Ntambi, James M
- Lusis, Aldons J
Producer: 20080610
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 28
Availability: No items available.
|
|
|
66.
|
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. [electronic resource] by
- Leppa, Virpi M
- Kravitz, Stephanie N
- Martin, Christa Lese
- Andrieux, Joris
- Le Caignec, Cedric
- Martin-Coignard, Dominique
- DyBuncio, Christina
- Sanders, Stephan J
- Lowe, Jennifer K
- Cantor, Rita M
- Geschwind, Daniel H
Producer: 20170502
In:
American journal of human genetics vol. 99
Availability: No items available.
|
|
|
67.
|
Genome-wide burden of deleterious coding variants increased in schizophrenia. [electronic resource] by
- Loohuis, Loes M Olde
- Vorstman, Jacob A S
- Ori, Anil P
- Staats, Kim A
- Wang, Tina
- Richards, Alexander L
- Leonenko, Ganna
- Walters, James T
- DeYoung, Joseph
- Cantor, Rita M
- Ophoff, Roel A
Producer: 20160419
In:
Nature communications vol. 6
Availability: No items available.
|
|
|
68.
|
DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype. [electronic resource] by
- Wang, Richard T
- Barthelemy, Florian
- Martin, Ann S
- Douine, Emilie D
- Eskin, Ascia
- Lucas, Ann
- Lavigne, Jenifer
- Peay, Holly
- Khanlou, Negar
- Sweeney, Lee
- Cantor, Rita M
- Miceli, M Carrie
- Nelson, Stanley F
Producer: 20190726
In:
Human mutation vol. 39
Availability: No items available.
|
|
|
69.
|
Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1. [electronic resource] by
- Huertas-Vazquez, Adriana
- Aguilar-Salinas, Carlos
- Lusis, Aldons J
- Cantor, Rita M
- Canizales-Quinteros, Samuel
- Lee, Jenny C
- Mariana-Nuñez, Lizzette
- Riba-Ramirez, Roopa-Metha Laura
- Jokiaho, Anne
- Tusie-Luna, Teresa
- Pajukanta, Päivi
Producer: 20060106
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 25
Availability: No items available.
|
|
|
70.
|
Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism. [electronic resource] by
- Suviolahti, Elina
- Reue, Karen
- Cantor, Rita M
- Phan, Jack
- Gentile, Massimiliano
- Naukkarinen, Jussi
- Soro-Paavonen, Aino
- Oksanen, Laura
- Kaprio, Jaakko
- Rissanen, Aila
- Salomaa, Veikko
- Kontula, Kimmo
- Taskinen, Marja-Riitta
- Pajukanta, Päivi
- Peltonen, Leena
Producer: 20060413
In:
Human molecular genetics vol. 15
Availability: No items available.
|
|
|
71.
|
Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan. [electronic resource] by
- Lin, Yi-Wen
- Hsu, Lea Chia-Ling
- Kuo, Pao-Lin
- Huang, William J
- Chiang, Han-Sun
- Yeh, Shauh-Der
- Hsu, Tuan-Yi
- Yu, Yueh-Hsiang
- Hsiao, Kuang-Nan
- Cantor, Rita M
- Yen, Pauline H
Producer: 20070621
In:
Human mutation vol. 28
Availability: No items available.
|
|
|
72.
|
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. [electronic resource] by
- Ogdie, Matthew N
- Macphie, I Laurence
- Minassian, Sonia L
- Yang, May
- Fisher, Simon E
- Francks, Clyde
- Cantor, Rita M
- McCracken, James T
- McGough, James J
- Nelson, Stanley F
- Monaco, Anthony P
- Smalley, Susan L
Producer: 20030701
In:
American journal of human genetics vol. 72
Availability: No items available.
|
|
|
73.
|
Association of the cannabinoid receptor gene (CNR1) with ADHD and post-traumatic stress disorder. [electronic resource] by
- Lu, Ake T
- Ogdie, Matthew N
- Järvelin, Marjo-Ritta
- Moilanen, Irma K
- Loo, Sandra K
- McCracken, James T
- McGough, James J
- Yang, May H
- Peltonen, Leena
- Nelson, Stanley F
- Cantor, Rita M
- Smalley, Susan L
Producer: 20090106
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 147B
Availability: No items available.
|
|
|
74.
|
Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated German multi-generation families. [electronic resource] by
- Lin, Michelle K
- Freitag, Christine M
- Schote, Andrea B
- Pálmason, Haukur
- Seitz, Christiane
- Renner, Tobias J
- Romanos, Marcel
- Walitza, Susanne
- Jacob, Christian P
- Reif, Andreas
- Warnke, Andreas
- Cantor, Rita M
- Lesch, Klaus-Peter
- Meyer, Jobst
Producer: 20141022
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 162B
Availability: No items available.
|
|
|
75.
|
Systems biology of the vervet monkey. [electronic resource] by
- Jasinska, Anna J
- Schmitt, Christopher A
- Service, Susan K
- Cantor, Rita M
- Dewar, Ken
- Jentsch, James D
- Kaplan, Jay R
- Turner, Trudy R
- Warren, Wesley C
- Weinstock, George M
- Woods, Roger P
- Freimer, Nelson B
Producer: 20140721
In:
ILAR journal vol. 54
Availability: No items available.
|
|
|
76.
|
Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans. [electronic resource] by
- Weissglas-Volkov, Daphna
- Plaisier, Christopher L
- Huertas-Vazquez, Adriana
- Cruz-Bautista, Ivette
- Riaño-Barros, Daniela
- Herrera-Hernandez, Miguel
- Riba, Laura
- Cantor, Rita M
- Sinsheimer, Janet S
- Aguilar-Salinas, Carlos A
- Tusie-Luna, Teresa
- Pajukanta, Päivi
Producer: 20100217
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 30
Availability: No items available.
|
|
|
77.
|
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1). [electronic resource] by
- Pajukanta, Päivi
- Lilja, Heidi E
- Sinsheimer, Janet S
- Cantor, Rita M
- Lusis, Aldons J
- Gentile, Massimiliano
- Duan, Xiaoqun Joyce
- Soro-Paavonen, Aino
- Naukkarinen, Jussi
- Saarela, Janna
- Laakso, Markku
- Ehnholm, Christian
- Taskinen, Marja-Riitta
- Peltonen, Leena
Producer: 20040816
In:
Nature genetics vol. 36
Availability: No items available.
|
|
|
78.
|
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. [electronic resource] by
- Alarcón, Maricela
- Abrahams, Brett S
- Stone, Jennifer L
- Duvall, Jacqueline A
- Perederiy, Julia V
- Bomar, Jamee M
- Sebat, Jonathan
- Wigler, Michael
- Martin, Christa L
- Ledbetter, David H
- Nelson, Stanley F
- Cantor, Rita M
- Geschwind, Daniel H
Producer: 20080130
In:
American journal of human genetics vol. 82
Availability: No items available.
|
|
|
79.
|
A genomewide screen of 345 families for autism-susceptibility loci. [electronic resource] by
- Yonan, Amanda L
- Alarcón, Maricela
- Cheng, Rong
- Magnusson, Patrik K E
- Spence, Sarah J
- Palmer, Abraham A
- Grunn, Adina
- Juo, Suh-Hang Hank
- Terwilliger, Joseph D
- Liu, Jianjun
- Cantor, Rita M
- Geschwind, Daniel H
- Gilliam, T Conrad
Producer: 20031121
In:
American journal of human genetics vol. 73
Availability: No items available.
|
|
|
80.
|
|