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Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements
Giglio, Sabrina, Broman, Karl W., Matsumoto, Naomichi, Calvari, Vladimiro, Gimelli, Giorgio, Neumann, Thomas, Ohashi, Hirofumi, Voullaire, Lucille, Larizza, Daniela, Giorda, Roberto, Weber, Jim L., Ledbetter, David H., Zuffardi, Orsetta
Published in American journal of human genetics (01.04.2001)
Published in American journal of human genetics (01.04.2001)
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microsatellite linkage map for Drosophila montana shows large variation in recombination rates, and a courtship song trait maps to an area of low recombination
SCHÄFER, M.A, MAZZI, D, KLAPPERT, K, KAURANEN, H, VIEIRA, J, HOIKKALA, A, RITCHIE, M.G, SCHLÖTTERER, C
Published in Journal of evolutionary biology (01.03.2010)
Published in Journal of evolutionary biology (01.03.2010)
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Complex evolutionary processes maintain an ancient chromosomal inversion
Nosil, Patrik, Soria-Carrasco, Victor, Villoutreix, Romain, De-la-Mora, Marisol, de Carvalho, Clarissa F., Parchman, Thomas, Feder, Jeffrey L., Gompert, Zachariah
Published in Proceedings of the National Academy of Sciences - PNAS (20.06.2023)
Published in Proceedings of the National Academy of Sciences - PNAS (20.06.2023)
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Tau and α-synuclein in susceptibility to, and dementia in, Parkinson's disease
Goris, An, Williams-Gray, Caroline H., Clark, Graeme R., Foltynie, Thomas, Lewis, Simon J. G., Brown, Joanne, Ban, Maria, Spillantini, Maria G., Compston, Alastair, Burn, David J., Chinnery, Patrick F., Barker, Roger A., Sawcer, Stephen J.
Published in Annals of neurology (01.08.2007)
Published in Annals of neurology (01.08.2007)
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Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation
Giglio, Sabrina, Calvari, Vladimiro, Gregato, Giuliana, Gimelli, Giorgio, Camanini, Silvia, Giorda, Roberto, Ragusa, Angela, Guerneri, Silvana, Selicorni, Angelo, Stumm, Marcus, Tonnies, Holger, Ventura, Mario, Zollino, Marcella, Neri, Giovanni, Barber, John, Wieczorek, Dagmar, Rocchi, Mariano, Zuffardi, Orsetta
Published in American journal of human genetics (01.08.2002)
Published in American journal of human genetics (01.08.2002)
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Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus
Demirci, F Yesim, Wang, Xingbin, Morris, David L, Feingold, Eleanor, Bernatsky, Sasha, Pineau, Christian, Clarke, Ann, Ramsey-Goldman, Rosalind, Manzi, Susan, Vyse, Timothy J, Ilyas Kamboh, M
Published in Journal of medical genetics (01.06.2017)
Published in Journal of medical genetics (01.06.2017)
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Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease
Zabetian, Cyrus P., Hutter, Carolyn M., Factor, Stewart A., Nutt, John G., Higgins, Donald S., Griffith, Alida, Roberts, John W., Leis, Berta C., Kay, Denise M., Yearout, Dora, Montimurro, Jennifer S., Edwards, Karen L., Samii, Ali, Payami, Haydeh
Published in Annals of neurology (01.08.2007)
Published in Annals of neurology (01.08.2007)
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Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases
Cervera-Carles, Laura, Pagonabarraga, Javier, Pascual-Sedano, Berta, Pastor, Pau, Campolongo, Antonia, Fortea, Juan, Blesa, Rafael, Alcolea, Daniel, Morenas-Rodríguez, Estrella, Sala, Isabel, Lleó, Alberto, Kulisevsky, Jaime, Clarimón, Jordi
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
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Comparative Genomic Analyses of the Human NPHP1 Locus Reveal Complex Genomic Architecture and Its Regional Evolution in Primates
Yuan, Bo, Liu, Pengfei, Gupta, Aditya, Beck, Christine R., Tejomurtula, Anusha, Campbell, Ian M., Gambin, Tomasz, Simmons, Alexandra D., Withers, Marjorie A., Harris, R. Alan, Rogers, Jeffrey, Schwartz, David C., Lupski, James R.
Published in PLoS genetics (01.12.2015)
Published in PLoS genetics (01.12.2015)
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Complex Genomic Rearrangements at the PLP1 Locus Include Triplication and Quadruplication
Beck, Christine R., Carvalho, Claudia M. B., Banser, Linda, Gambin, Tomasz, Stubbolo, Danielle, Yuan, Bo, Sperle, Karen, McCahan, Suzanne M., Henneke, Marco, Seeman, Pavel, Garbern, James Y., Hobson, Grace M., Lupski, James R.
Published in PLoS genetics (01.03.2015)
Published in PLoS genetics (01.03.2015)
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Observation of a parental inversion variant in a rare Williams–Beuren syndrome family with two affected children
Scherer, Stephen W., Gripp, Karen W., Lucena, Jaume, Nicholson, Linda, Bonnefont, Jean-Paul, Pérez-Jurado, Luis A., Osborne, Lucy R.
Published in Human genetics (01.08.2005)
Published in Human genetics (01.08.2005)
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