Associations between a risky psychosocial childhood and recurrent addiction compulsory care as adult

por Grahn, Robert, Padyab, Mojgan, Lundgren, Lena
Publicado 2019

Compulsory care of individuals with severe substance use disorders and alcohol- and drug-related mortality: A Swedish registry study

por Scarpa, Simone, Grahn, Robert, Lundgren, Lena M.
Publicado 2023

Two Variants in SLC24A5 Are Associated with “Tiger-Eye” Iris Pigmentation in Puerto Rican Paso Fino Horses

por Mack, Maura, Kowalski, Elizabeth, Grahn, Robert, Bras, Dineli, Penedo, Maria Cecilia T., Bellone, Rebecca
Publicado 2017

Genetic heterogeneity and diversity of North American golden retrievers using a low density STR marker panel

por Ontiveros, Eric S., Hughes, Shayne, Penedo, Maria Cecilia T., Grahn, Robert A., Stern, Joshua A.
Publicado 2019

Pigment Intensity in Dogs is Associated with a Copy Number Variant Upstream of KITLG

por Weich, Kalie, Affolter, Verena, York, Daniel, Rebhun, Robert, Grahn, Robert, Kallenberg, Angelica, Bannasch, Danika
Publicado 2020

Erythrocyte Pyruvate Kinase Deficiency mutation identified in multiple breeds of domestic cats

por Grahn, Robert A, Grahn, Jennifer C, Penedo, Maria CT, Helps, Chris R, Lyons, Leslie A
Publicado 2012

Mucopolysaccharidosis VI in cats – clarification regarding genetic testing

por Lyons, Leslie A., Grahn, Robert A., Genova, Francesca, Beccaglia, Michela, Hopwood, John J., Longeri, Maria
Publicado 2016

SNP Miniplexes for Individual Identification of Random‐Bred Domestic Cats

por Brooks, Ashley, Creighton, Erica K., Gandolfi, Barbara, Khan, Razib, Grahn, Robert A., Lyons, Leslie A.
Publicado 2016

Correction: Weich, K., et al. Pigment Intensity in Dogs Is Associated with a Copy Number Variant Upstream of KITLG. Genes 2020, 11, 75

por Bannasch, Danika L., Affolter, Verena K., York, Daniel, Rebhun, Robert B., Grahn, Robert A., Weich, Kalie M., Kallenberg, Angelica
Publicado 2021

Cytidine monophospho-N-acetylneuraminic acid hydroxylase (CMAH) mutations associated with the domestic cat AB blood group

por Bighignoli, Barbara, Niini, Tirri, Grahn, Robert A, Pedersen, Niels C, Millon, Lee V, Polli, Michele, Longeri, Maria, Lyons, Leslie A
Publicado 2007

The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71

por Gandolfi, Barbara, Outerbridge, Catherine A., Beresford, Leslie G., Myers, Jeffrey A., Pimentel, Monica, Alhaddad, Hasan, Grahn, Jennifer C., Grahn, Robert A., Lyons, Leslie A.
Publicado 2010

A Novel Variant in CMAH Is Associated with Blood Type AB in Ragdoll Cats

por Gandolfi, Barbara, Grahn, Robert A., Gustafson, Nicholas A., Proverbio, Daniela, Spada, Eva, Adhikari, Badri, Cheng, Janling, Andrews, Gordon, Lyons, Leslie A., Helps, Chris R.
Publicado 2016

Correction: A Novel Variant in CMAH Is Associated with Blood Type AB in Ragdoll Cats

por Gandolfi, Barbara, Grahn, Robert A., Gustafson, Nicholas A., Proverbio, Daniela, Spada, Eva, Adhikari, Badri, Cheng, Janling, Andrews, Gordon, Lyons, Leslie A., Helps, Chris R.
Publicado 2018

Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats

por Alhaddad, Hasan, Gandolfi, Barbara, Grahn, Robert A., Rah, Hyung-Chul, Peterson, Carlyn B., Maggs, David J., Good, Kathryn L., Pedersen, Niels C., Lyons, Leslie A.
Publicado 2014

Whole genome sequencing in cats, identifies new models for blindness in AIPL1 and somite segmentation in HES7

por Lyons, Leslie A., Creighton, Erica K., Alhaddad, Hasan, Beale, Holly C., Grahn, Robert A., Rah, HyungChul, Maggs, David J., Helps, Christopher R., Gandolfi, Barbara
Publicado 2016

A Third MLPH Variant Causing Coat Color Dilution in Dogs

por Van Buren, Samantha L., Minor, Katie M., Grahn, Robert A., Mickelson, James R., Grahn, Jennifer C., Malvick, Julia, Colangelo, Jennifer R., Mueller, Elisabeth, Kuehnlein, Petra, Kehl, Alexandra
Publicado 2020

Extent of Linkage Disequilibrium in the Domestic Cat, Felis silvestris catus, and Its Breeds

por Alhaddad, Hasan, Khan, Razib, Grahn, Robert A., Gandolfi, Barbara, Mullikin, James C., Cole, Shelley A., Gruffydd-Jones, Timothy J., Häggström, Jens, Lohi, Hannes, Longeri, Maria, Lyons, Leslie A.
Publicado 2013

COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy

por Gandolfi, Barbara, Grahn, Robert A., Creighton, Erica K., Williams, D. Colette, Dickinson, Peter J., Sturges, Beverly K., Guo, Ling T., Shelton, G. Diane, Leegwater, Peter A. J., Longeri, Maria, Malik, Richard, Lyons, Leslie A.
Publicado 2015

A High-Resolution SNP Array-Based Linkage Map Anchors a New Domestic Cat Draft Genome Assembly and Provides Detailed Patterns of Recombination

por Li, Gang, Hillier, LaDeana W., Grahn, Robert A., Zimin, Aleksey V., David, Victor A., Menotti-Raymond, Marilyn, Middleton, Rondo, Hannah, Steven, Hendrickson, Sher, Makunin, Alex, O’Brien, Stephen J., Minx, Pat, Wilson, Richard K., Lyons, Leslie A., Warren, Wesley C., Murphy, William J.
Publicado 2016

Increased α‐tocopherol metabolism in horses with equine neuroaxonal dystrophy

por Hales, Erin N., Habib, Hadi, Favro, Gianna, Katzman, Scott, Sakai, R. Russell, Marquardt, Sabin, Bordbari, Matthew H., Ming‐Whitfield, Brittni, Peterson, Janel, Dahlgren, Anna R., Rivas, Victor, Ramirez, Carolina Alanis, Peng, Sichong, Donnelly, Callum G., Dizmang, Bobbi‐Sue, Kallenberg, Angelica, Grahn, Robert, Miller, Andrew D., Woolard, Kevin, Moeller, Benjamin, Puschner, Birgit, Finno, Carrie J.
Publicado 2021