Multipoint Lods Provide Reliable Linkage Evidence Despite Unknown Limiting Distribution: Type I Error Probabilities Decrease with Sample Size for Multipoint Lods and Mods

ανά Hodge, Susan E., Rodriguez-Murillo, Laura, Strug, Lisa J., Greenberg, David A.
Έκδοση 2008

Fine Mapping on Chromosome 13q32–34 and Brain Expression Analysis Implicates MYO16 in Schizophrenia

ανά Rodriguez-Murillo, Laura, Xu, Bin, Roos, J Louw, Abecasis, Gonçalo R, Gogos, Joseph A, Karayiorgou, Maria
Έκδοση 2014

Intraoperative radiation therapy, opportunities for clinical practice normalization: MEDTING, a scientific platform

ανά Calvo, Felipe A., Murillo, Laura Alonso, Sallabanda, Morena, Martinez-Villanueva, Javier, Herranz, Rafael, Sole, Claudio V.
Έκδοση 2013

C9ORF72 repeat expansions not detected in a group of patients with schizophrenia

ανά Huey, Edward D., Nagy, Peter L., Rodriguez-Murillo, Laura, Manochehri, Masood, Goldman, Jill, Lieberman, Jeffrey, Karayiorgou, Maria, Mayeux, Richard
Έκδοση 2012

Role of Connexins 30, 36, and 43 in Brain Tumors, Neurodegenerative Diseases, and Neuroprotection

ανά Sánchez, Oscar F., Rodríguez, Andrea V., Velasco-España, José M., Murillo, Laura C., Sutachan, Jhon-Jairo, Albarracin, Sonia-Luz
Τόπος έκδοσης Cells (2020)

Prognostic Significance of Deregulated Dicer Expression in Breast Cancer

ανά Caffrey, Emer, Ingoldsby, Helen, Wall, Deirdre, Webber, Mark, Dinneen, Kate, Murillo, Laura S., Inderhaug, Celine, Newell, John, Gupta, Sanjeev, Callagy, Grace
Έκδοση 2013

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

ανά Xu, Bin, Woodroffe, Abigail, Rodriguez-Murillo, Laura, Roos, J. Louw, van Rensburg, Elizabeth J., Abecasis, Gonçalo R., Gogos, Joseph A., Karayiorgou, Maria
Έκδοση 2009

Novel loci interacting epistatically with Bone Morphogenetic Protein Receptor 2 cause familial pulmonary arterial hypertension

ανά Rodriguez-Murillo, Laura, Subaran, Ryan, Stewart, William C. L., Pramanik, Sreemanta, Marathe, Sudhir, Barst, Robyn J., Chung, Wendy K., Greenberg, David A.
Έκδοση 2009

CANOES: detecting rare copy number variants from whole exome sequencing data

ανά Backenroth, Daniel, Homsy, Jason, Murillo, Laura R., Glessner, Joe, Lin, Edwin, Brueckner, Martina, Lifton, Richard, Goldmuntz, Elizabeth, Chung, Wendy K., Shen, Yufeng
Έκδοση 2014

A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure

ανά Granot-Hershkovitz, Einat, Karasik, David, Friedlander, Yechiel, Rodriguez-Murillo, Laura, Dorajoo, Rajkumar, Liu, Jianjun, Sewda, Anshuman, Peter, Inga, Carmi, Shai, Hochner, Hagit
Τόπος έκδοσης Eur J Hum Genet (2018)

Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity

ανά Garcia, John, Tahiliani, Jackie, Johnson, Nicole Marie, Aguilar, Sienna, Beltran, Daniel, Daly, Amy, Decker, Emily, Haverfield, Eden, Herrera, Blanca, Murillo, Laura, Nykamp, Keith, Topper, Scott
Τόπος έκδοσης Front Cardiovasc Med (2016)

A High Through-Put Screen for Small Molecules Modulating MCM2 Phosphorylation Identifies Ryuvidine as an Inducer of the DNA Damage Response

ανά FitzGerald, Jennifer, Murillo, Laura S., O'Brien, Gemma, O'Connell, Enda, O'Connor, Aisling, Wu, Kevin, Wang, Guan-Nan, Rainey, Michael D., Natoni, Alessandro, Healy, Sandra, O'Dwyer, Michael, Santocanale, Corrado
Έκδοση 2014

Intraoperative radiation therapy opportunities for clinical practice normalization: Data recording and innovative development

ανά Calvo, Felipe A., Sallabanda, Morena, Sole, Claudio V., Gonzalez, Carmen, Murillo, Laura Alonso, Martinez-Villanueva, Javier, Santos, Juan A., Serrano, Javier, Alavrez, Ana, Blanco, Jose, Calin, Ana, Gomez-Espi, Marina, Lozano, Miguel, Herranz, Rafael
Έκδοση 2013

The caveolae‐associated coiled‐coil protein, NECC2, regulates insulin signalling in Adipocytes

ανά Trávez, Andrés, Rabanal‐Ruiz, Yoana, López‐Alcalá, Jaime, Molero‐Murillo, Laura, Díaz‐Ruiz, Alberto, Guzmán‐Ruiz, Rocío, Catalán, Victoria, Rodríguez, Amaia, Frühbeck, Gema, Tinahones, Francisco J., Gasman, Stéphane, Vitale, Nicolas, Jiménez‐Gómez, Yolanda, Malagón, María M.
Τόπος έκδοσης J Cell Mol Med (2018)

The sialyltransferase ST3GAL6 influences homing and survival in multiple myeloma

ανά Glavey, Siobhan V., Manier, Salomon, Natoni, Alessandro, Sacco, Antonio, Moschetta, Michele, Reagan, Michaela R., Murillo, Laura S., Sahin, Ilyas, Wu, Ping, Mishima, Yuji, Zhang, Yu, Zhang, Wenjing, Zhang, Yong, Morgan, Gareth, Joshi, Lokesh, Roccaro, Aldo M., Ghobrial, Irene M., O’Dwyer, Michael E.
Έκδοση 2014

PNR-16 DIAGNOSIS, MANAGEMENT AND OUTCOME OF CHILDREN WITH CENTRAL NERVOUS SYSTEM (CNS) PRIMITIVE NEUROECTODERMAL TUMORS (PNET) IN SPAIN: A STUDY FROM THE SPANISH NATIONAL PEDIATRIC...

ανά de Rojas, Teresa, Bautista, Francisco José, Flores, Miguel, Fioravantti, Victoria, Igual, Lucía, Rubio, Raquel, Bardón, Eduardo, Navarro, Lucía, Murillo, Laura, Hladun, Raquel, Cañete, Adela, García, Miguel, Garrido, Carmen, Fernández-Teijeiro, Ana, Quiroga, Eduardo, Calvo, Carlota, Llort, Anna, Madero, Luis, Cruz, Ofelia, Moreno, Lucas
Τόπος έκδοσης Neuro Oncol (2016)

Oral metronomic vinorelbine combined with endocrine therapy in hormone receptor-positive HER2-negative breast cancer: SOLTI-1501 VENTANA window of opportunity trial

ανά Adamo, Barbara, Bellet, Meritxell, Paré, Laia, Pascual, Tomás, Vidal, Maria, Pérez Fidalgo, José A., Blanch, Salvador, Martinez, Noelia, Murillo, Laura, Gómez-Pardo, Patricia, López-González, Ana, Amillano, Kepa, Canes, Jordi, Galván, Patricia, González-Farré, Blanca, González, Xavier, Villagrasa, Patricia, Ciruelos, Eva, Prat, Aleix
Τόπος έκδοσης Breast Cancer Res (2019)

Increased Frequency of De Novo Copy Number Variations in Congenital Heart Disease by Integrative Analysis of SNP Array and Exome Sequence Data

ανά Glessner, Joseph T., Bick, Alexander G., Ito, Kaoru, Homsy, Jason, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R., Golhar, Ryan, Sanders, Stephan J., Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A. Jeremy, State, Matthew W., Kaltman, Jonathan R., White, Peter S., Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D., Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K.
Έκδοση 2014

Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk

ανά Rafnar, Thorunn, Sulem, Patrick, Besenbacher, Soren, Gudbjartsson, Daniel F., Zanon, Carlo, Gudmundsson, Julius, Stacey, Simon N., Kostic, Jelena P., Thorgeirsson, Thorgeir E., Thorleifsson, Gudmar, Bjarnason, Hjordis, Skuladottir, Halla, Gudbjartsson, Tomas, Isaksson, Helgi J., Isla, Dolores, Murillo, Laura, García-Prats, Maria D., Panadero, Angeles, Aben, Katja K.H., Vermeulen, Sita H., van der Heijden, Henricus F.M., Feser, William, Miller, York E., Bunn, Paul A., Kong, Augustine, Wolf, Holly J., Franklin, Wilbur A., Mayordomo, Jose I, Kiemeney, Lambertus A., Jonsson, Steinn, Thorsteinsdottir, Unnur, Stefansson, Kari
Έκδοση 2011

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

ανά Gudmundsson, Julius, Sulem, Patrick, Gudbjartsson, Daniel F., Blondal, Thorarinn, Gylfason, Arnaldur, Agnarsson, Bjarni A., Benediktsdottir, Kristrun R., Magnusdottir, Droplaug N., Orlygsdottir, Gudbjorg, Jakobsdottir, Margret, Stacey, Simon N., Sigurdsson, Asgeir, Wahlfors, Tiina, Tammela, Teuvo, Breyer, Joan P., McReynolds, Kate M., Bradley, Kevin M., Saez, Berta, Godino, Javier, Navarrete, Sebastian, Fuertes, Fernando, Murillo, Laura, Polo, Eduardo, Aben, Katja K., van Oort, Inge M., Suarez, Brian K., Helfand, Brian T., Kan, Donghui, Zanon, Carlo, Frigge, Michael L., Kristjansson, Kristleifur, Gulcher, Jeffrey R., Einarsson, Gudmundur V., Jonsson, Eirikur, Catalona, William J., Mayordomo, Jose I., Kiemeney, Lambertus A., Smith, Jeffrey R., Schleutker, Johanna, Barkardottir, Rosa B., Kong, Augustine, Thorsteinsdottir, Unnur, Rafnar, Thorunn, Stefansson, Kari
Έκδοση 2009