Search Results

Natural re-colonization and admixture of wolves (Canis lupus) in the US Pacific Northwest: challenges for the protection and management of rare and endangered taxa

by Hendricks, Sarah A., Schweizer, Rena M., Harrigan, Ryan J., Pollinger, John P., Paquet, Paul C., Darimont, Chris T., Adams, Jennifer R., Waits, Lisette P., vonHoldt, Bridgett M., Hohenlohe, Paul A., Wayne, Robert K.
Published in Heredity (2018)

Adenylate kinase polymorphism in populations in Finland (Swedes, Finns, Lapps), in Maris, and in Greenland Eskimos

by Eriksson, A. W., Fellman, J., Kirjarinta, M., Eskola, Marja-Riitta, Singh, S., Benkmann, Heide-G., Goedde, H. W., Mourant, A. E., Tills, D., Lehmann, W.
Published in Human Genetics (1971)

Uncovering the Genetic History of the Present-Day Greenlandic Population

by Moltke, Ida, Fumagalli, Matteo, Korneliussen, Thorfinn S., Crawford, Jacob E., Bjerregaard, Peter, Jørgensen, Marit E., Grarup, Niels, Gulløv, Hans Christian, Linneberg, Allan, Pedersen, Oluf, Hansen, Torben, Nielsen, Rasmus, Albrechtsen, Anders
Published in The American Journal of Human Genetics (2015)

Cultural Transmission of Fine-Scale Fidelity to Feeding Sites May Shape Humpback Whale Genetic Diversity in Russian Pacific Waters

by Richard, Gaëtan, Titova, Olga V, Fedutin, Ivan D, Steel, Debbie, Meschersky, Ilya G, Hautin, Marie, Burdin, Alexander M, Hoyt, Erich, Filatova, Olga A, Jung, Jean-Luc
Published in Journal of Heredity (2018)

Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan Eskimos

by Voruganti, V. Saroja, Higgins, Paul B., Ebbesson, Sven O. E., Kennish, John, Göring, Harald H. H., Haack, Karin, Laston, Sandra, Drigalenko, Eugene, Wenger, Charlotte R., Harris, William S., Fabsitz, Richard R., Devereux, Richard B., MacCluer, Jean W., Curran, Joanne E., Carless, Melanie A., Johnson, Matthew P., Moses, Eric K., Blangero, John, Umans, Jason G., Howard, Barbara V., Cole, Shelley A., Comuzzie, Anthony Gean
Published in Frontiers in Genetics (2012)

Both rare and common genetic variants contribute to autism in the Faroe Islands

by Leblond, Claire S, Cliquet, Freddy, Carton, Coralie, Huguet, Guillaume, Mathieu, Alexandre, Kergrohen, Thomas, Buratti, Julien, Lemière, Nathalie, Cuisset, Laurence, Bienvenu, Thierry, Boland, Anne, Deleuze, Jean-François, Stora, Tormodur, Biskupstoe, Rannva, Halling, Jónrit, Andorsdóttir, Guðrið, Billstedt, Eva, Gillberg, Christopher, Bourgeron, Thomas
Published in npj Genomic Medicine (2019)

VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families

by Bourassa, Cynthia V., Meijer, Inge A., Merner, Nancy D., Grewal, Kanwal K., Stefanelli, Mark G., Hodgkinson, Kathleen, Ives, Elizabeth J., Pryse-Phillips, William, Jog, Mandar, Boycott, Kym, Grimes, David A., Goobie, Sharan, Leckey, Richard, Dion, Patrick A., Rouleau, Guy A.
Published in The American Journal of Human Genetics (2012)

Rhodopsin Gene Polymorphism Associated with Divergent Light Environments in Atlantic Cod

by Pampoulie, Christophe, Skirnisdottir, Sigurlaug, Star, Bastiaan, Jentoft, Sissel, Jónsdóttir, Ingibjörg G., Hjörleifsson, Einar, Thorsteinsson, Vilhjálmur, Pálsson, Ólafur K., Berg, Paul R., Andersen, Øivind, Magnusdottir, Steinunn, Helyar, Sarah J., Daníelsdóttir, Anna K.
Published in Behavior Genetics (2015)

Mitochondrial Genome Diversity in Arctic Siberians, with Particular Reference to the Evolutionary History of Beringia and Pleistocenic Peopling of the Americas

by Volodko, Natalia V., Starikovskaya, Elena B., Mazunin, Ilya O., Eltsov, Nikolai P., Naidenko, Polina V., Wallace, Douglas C., Sukernik, Rem I.
Published in The American Journal of Human Genetics (2008)

Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan

by Ahmed, Zubair M, Cindy Li, Xiaoyan, Powell, Shontell D, Riazuddin, Saima, Young, Terry-Lynn, Ramzan, Khushnooda, Ahmad, Zahoor, Luscombe, Sandra, Dhillon, Kiran, MacLaren, Linda, Ploplis, Barbara, Shotland, Lawrence I, Ives, Elizabeth, Riazuddin, Sheikh, Friedman, Thomas B, Morell, Robert J, Wilcox, Edward R
Published in BMC Medical Genetics (2004)

Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

by Barashkov, Nikolay A., Konovalov, Fedor A., Borisova, Tuyara V., Teryutin, Fedor M., Solovyev, Aisen V., Pshennikova, Vera G., Sapojnikova, Nadejda V., Vychuzhina, Lyubov S., Romanov, Georgii P., Gotovtsev, Nyurgun N., Morozov, Igor V., Bondar, Alexander A., Platonov, Fedor A., Burtseva, Tatiana E., Khusnutdinova, Elza K., Posukh, Olga L., Fedorova, Sardana A.
Published in European Journal of Human Genetics (2021)

Iceland—Genetic Counseling Services

by Stefansdottir, Vigdis, Arngrimsson, Reynir, Jonsson, Jon J.
Published in Journal of Genetic Counseling (2013)

A Selective Sweep on a Deleterious Mutation in CPT1A in Arctic Populations

by Clemente, Florian J., Cardona, Alexia, Inchley, Charlotte E., Peter, Benjamin M., Jacobs, Guy, Pagani, Luca, Lawson, Daniel J., Antão, Tiago, Vicente, Mário, Mitt, Mario, DeGiorgio, Michael, Faltyskova, Zuzana, Xue, Yali, Ayub, Qasim, Szpak, Michal, Mägi, Reedik, Eriksson, Anders, Manica, Andrea, Raghavan, Maanasa, Rasmussen, Morten, Rasmussen, Simon, Willerslev, Eske, Vidal-Puig, Antonio, Tyler-Smith, Chris, Villems, Richard, Nielsen, Rasmus, Metspalu, Mait, Malyarchuk, Boris, Derenko, Miroslava, Kivisild, Toomas
Published in The American Journal of Human Genetics (2014)

Barriers to access to and uptake of genetic services from the perspectives of genetic professionals

by Darmonkow, Valerie Zdravka
Published 2012

The Western and Eastern Roots of the Saami—the Story of Genetic “Outliers” Told by Mitochondrial DNA and Y Chromosomes

by Tambets, Kristiina, Rootsi, Siiri, Kivisild, Toomas, Help, Hela, Serk, Piia, Loogväli, Eva-Liis, Tolk, Helle-Viivi, Reidla, Maere, Metspalu, Ene, Pliss, Liana, Balanovsky, Oleg, Pshenichnov, Andrey, Balanovska, Elena, Gubina, Marina, Zhadanov, Sergey, Osipova, Ludmila, Damba, Larisa, Voevoda, Mikhail, Kutuev, Ildus, Bermisheva, Marina, Khusnutdinova, Elza, Gusar, Vladislava, Grechanina, Elena, Parik, Jüri, Pennarun, Erwan, Richard, Christelle, Chaventre, Andre, Moisan, Jean-Paul, Barać, Lovorka, Peričić, Marijana, Rudan, Pavao, Terzić, Rifat, Mikerezi, Ilia, Krumina, Astrida, Baumanis, Viesturs, Koziel, Slawomir, Rickards, Olga, De Stefano, Gian Franco, Anagnou, Nicholas, Pappa, Kalliopi I., Michalodimitrakis, Emmanuel, Ferák, Vladimir, Füredi, Sandor, Komel, Radovan, Beckman, Lars, Villems, Richard
Published in The American Journal of Human Genetics (2004)

Intergeneric hybridization of two stickleback species leads to introgression of membrane-associated genes and invasive TE expansion

by Nedoluzhko, Artem, Sharko, Fedor, Tsygankova, Svetlana, Boulygina, Eugenia, Slobodova, Natalia, Teslyuk, Anton, Galindo-Villegas, Jorge, Rastorguev, Sergey
Published in Frontiers in Genetics (2022)

GENETIC CONTROL OF THE IMMUNE RESPONSE TO MYOGLOBIN: VIII. CONTROL OF ANTIBODY AFFINITY

by Young, C. R., O'Connor, G. P., Atassi, M. Z.
Published in European Journal of Immunogenetics (1981)

Common ancestral mutations in theMEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland

by Olufemi, Shodimu-Emmanuel, Green, Jane S., Manickam, Pachiappan, Guru, Siradanahalli C., Agarwal, Sunita K., Kester, Mary Beth, Dong, Qihan, Burns, A. Lee, Spiegel, Allen M., Marx, Stephen J., Collins, Francis S., Chandrasekharappa, Settara C.
Published 1998

THE ASSOCIATION BETWEEN COELIAC DISEASE, DERMATITIS HERPETIFORMIS AND CERTAIN HLA‐ANTIGENS IN ICELANDERS

by ÁRnason, A., Skaftadóttir, I., Sigmundsson, J., MOONEY, E., Björnsson, J., Cariglia, N., Pálsson, G., Gudjónsson, H.
Published in International Journal of Immunogenetics (1994)

Identification and Characterization of DNA Demethylase Genes and Their Association With Thermal Stress in Wheat (Triticum aestivum L.)

by Gahlaut, Vijay, Samtani, Harsha, Gautam, Tinku, Khurana, Paramjit
Published in Frontiers in Genetics (2022)