Prenatal Screening for Genetic Defects

Por Cann, Howard
Publicado em 1976

A Symposium on Pesticides: Pesticide Poisoning Accidents Among Young Children

Por Cann, Howard M.
Publicado em 1963

Advances in human genetics

Por Cann, Howard M.
Publicado em 1977

Segregation Analysis of Juvenile Diabetes Mellitus

Por Barrai, Italo, Cann, Howard M.
Publicado em 1965

IN VITRO STUDIES OF MAMMALIAN SOMATIC CELL VARIATION : II. ISOIMMUNE CYTOTOXICITY WITH A CULTURED MOUSE LYMPHOMA AND SELECTION OF RESISTANT VARIANTS

Por Cann, Howard M., Herzenberg, Leonard A.
Publicado em 1963

IN VITRO STUDIES OF MAMMALIAN SOMATIC CELL VARIATION : I. DETECTION OF H-2 PHENOTYPE IN CULTURED MOUSE CELL LINES

Por Cann, Howard M., Herzenberg, Leonard A.
Publicado em 1963

Epidemiologic Aspects of Poisoning Accidents

Por Cann, Howard M., Iskrant, Albert P., Neyman, Dorothy S.
Publicado em 1960

JEAN B DAUSSET, 19 OCTOBER 1916–6 JUNE 2009

Por Mandel, Jean-Louis, Lathrop, Mark, Cann, Howard M
Publicado em 2009

Segregation analysis of hemophilia A and B

Por Barrai, Italo, Cann, Howard M., Cavalli-Sforza, Luigi Luca
Publicado em 1979

Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?

Por Leutenegger, Anne-Louise, Sahbatou, Mourad, Gazal, Steven, Cann, Howard, Génin, Emmanuelle
Publicado em 2011

The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L Region

Por Barreiro, Luis B. , Patin, Etienne , Neyrolles, Olivier , Cann, Howard M. , Gicquel, Brigitte , Quintana-Murci, Lluís 
Publicado em 2005

Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22

Por González-Neira, Anna, Calafell, Francesc, Navarro, Arcadi, Lao, Oscar, Cann, Howard, Comas, David, Bertranpetit, Jaume
Publicado em 2004

Positive Selection in the Chromosome 16 VKORC1 Genomic Region Has Contributed to the Variability of Anticoagulant Response in Humans

Por Patillon, Blandine, Luisi, Pierre, Blanché, Hélène, Patin, Etienne, Cann, Howard M., Génin, Emmanuelle, Sabbagh, Audrey
Publicado em 2012

Marked Phenotypic Heterogeneity Associated with Expansion of a CAG Repeat Sequence at the Spinocerebellar Ataxia 3/Machado-Joseph Disease Locus

Por Cancel, Géraldine, Abbas, Nacer, Stevanin, Giovanni, Dürr, Alexandra, Chneiweiss, Hervé, Néri, Christian, Duyckaerts, Charles, Penet, Christiane, Cann, Howard M., Agid, Yves, Brice, Alexis
Publicado em 1995

The portability of tagSNPs across populations: A worldwide survey

Por González-Neira, Anna, Ke, Xiayi, Lao, Oscar, Calafell, Francesc, Navarro, Arcadi, Comas, David, Cann, Howard, Bumpstead, Suzannah, Ghori, Jilur, Hunt, Sarah, Deloukas, Panos, Dunham, Ian, Cardon, Lon R., Bertranpetit, Jaume
Publicado em 2006

Transcriptome Sequencing from Diverse Human Populations Reveals Differentiated Regulatory Architecture

Por Martin, Alicia R., Costa, Helio A., Lappalainen, Tuuli, Henn, Brenna M., Kidd, Jeffrey M., Yee, Muh-Ching, Grubert, Fabian, Cann, Howard M., Snyder, Michael, Montgomery, Stephen B., Bustamante, Carlos D.
Publicado em 2014

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds

Por Zoghbi, Huda Y., Jodice, Carla, Sandkuijl, Lodewijk A., Kwiatkowski, Thomas J., McCall, Alanna E., Huntoon, Sally A., Lulli, Patrizia, Spadaro, Maria, Litt, Michael, Cann, Howard M., Frontali, Marina, Terrenato, Luciano
Publicado em 1991

Distance from sub-Saharan Africa predicts mutational load in diverse human genomes

Por Henn, Brenna M., Botigué, Laura R., Peischl, Stephan, Dupanloup, Isabelle, Lipatov, Mikhail, Maples, Brian K., Martin, Alicia R., Musharoff, Shaila, Cann, Howard, Snyder, Michael P., Excoffier, Laurent, Kidd, Jeffrey M., Bustamante, Carlos D.
Publicado no Proc Natl Acad Sci U S A (2016)

A 3.9-Centimorgan-Resolution Human Single-Nucleotide Polymorphism Linkage Map and Screening Set

Por Matise, Tara C., Sachidanandam, Ravi, Clark, Andrew G., Kruglyak, Leonid, Wijsman, Ellen, Kakol, Jerzy, Buyske, Steven, Chui, Buena, Cohen, Patrick, Toma, Claudia de, Ehm, Margaret, Glanowski, Stephen, He, Chunsheng, Heil, Jeremy, Markianos, Kyriacos, McMullen, Ivy, Pericak-Vance, Margaret A., Silbergleit, Arkadiy, Stein, Lincoln, Wagner, Michael, Wilson, Alexander F., Winick, Jeffrey D., Winn-Deen, Emily S., Yamashiro, Carl T., Cann, Howard M., Lai, Eric, Holden, Arthur L.
Publicado em 2003

The complete genome sequence of a Neandertal from the Altai Mountains

Por Prüfer, Kay, Racimo, Fernando, Patterson, Nick, Jay, Flora, Sankararaman, Sriram, Sawyer, Susanna, Heinze, Anja, Renaud, Gabriel, Sudmant, Peter H., de Filippo, Cesare, Li, Heng, Mallick, Swapan, Dannemann, Michael, Fu, Qiaomei, Kircher, Martin, Kuhlwilm, Martin, Lachmann, Michael, Meyer, Matthias, Ongyerth, Matthias, Siebauer, Michael, Theunert, Christoph, Tandon, Arti, Moorjani, Priya, Pickrell, Joseph, Mullikin, James C., Vohr, Samuel H., Green, Richard E., Hellmann, Ines, Johnson, Philip L. F., Blanche, Hélène, Cann, Howard, Kitzman, Jacob O., Shendure, Jay, Eichler, Evan E., Lein, Ed S., Bakken, Trygve E., Golovanova, Liubov V., Doronichev, Vladimir B., Shunkov, Michael V., Derevianko, Anatoli P., Viola, Bence, Slatkin, Montgomery, Reich, David, Kelso, Janet, Pääbo, Svante
Publicado em 2013