Efficient Multipoint Linkage Analysis through Reduction of Inheritance Space

Por Markianos, Kyriacos, Daly, Mark J., Kruglyak, Leonid
Publicado em 2001

No Bias in Linkage Analysis

Por Abecasis, Goncalo, Cox, Nancy, Daly, Mark J., Kruglyak, Leonid, Laird, Nan, Markianos, Kyriacos, Patterson, Nick
Publicado em 2004

A major genetic locus controlling natural Plasmodium falciparum infection is shared by East and West African Anopheles gambiae

Por Riehle, Michelle M, Markianos, Kyriacos, Lambrechts, Louis, Xia, Ai, Sharakhov, Igor, Koella, Jacob C, Vernick, Kenneth D
Publicado em 2007

Sequence-Based Linkage Analysis

Por Furman, Itay, Rieder, Mark J., da Ponte, Suzanne, Carrington, Dana P., Nickerson, Deborah A., Kruglyak, Leonid, Markianos, Kyriacos
Publicado em 2004

A Novel Rat Model of Hereditary Hemochromatosis Due to a Mutation in Transferrin Receptor 2

Por Bartnikas, Thomas B, Wildt, Sheryl J, Wineinger, Amy E, Schmitz-Abe, Klaus, Markianos, Kyriacos, Cooper, Dale M, Fleming, Mark D
Publicado em 2013

The kdr-bearing haplotype and susceptibility to Plasmodium falciparum in Anopheles gambiae: genetic correlation and functional testing

Por Mitri, Christian, Markianos, Kyriacos, Guelbeogo, Wamdaogo M., Bischoff, Emmanuel, Gneme, Awa, Eiglmeier, Karin, Holm, Inge, Sagnon, N’Fale, Vernick, Kenneth D., Riehle, Michelle M.
Publicado no Malar J (2015)

Genetic Structure of a Local Population of the Anopheles gambiae Complex in Burkina Faso

Por Markianos, Kyriacos, Bischoff, Emmanuel, Mitri, Christian, Guelbeogo, Wamdaogo M., Gneme, Awa, Eiglmeier, Karin, Holm, Inge, Sagnon, N’Fale, Vernick, Kenneth D., Riehle, Michelle M.
Publicado no PLoS One (2016)

The Serotonin-Related FEV Gene Variant in the Sudden Infant Death Syndrome is a Common Polymorphism in the African–American Population

Por Broadbelt, Kevin G., Barger, Melissa A., Paterson, David S., Holm, Ingrid A., Haas, Elisabeth A., Krous, Henry F., Kinney, Hannah C., Markianos, Kyriacos, Beggs, Alan H.
Publicado em 2009

Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants

Por Morton, Sarah U., Neilan, Edward G., Peake, Roy W. A., Shi, Jiahai, Schmitz-Abe, Klaus, Towne, Meghan, Markianos, Kyriacos, Prabhu, Sanjay P., Agrawal, Pankaj B.
Publicado no JIMD Rep (2016)

Expanding the Phenotype Associated With the NEFL Mutation Neuromuscular Disease in a Family with Overlapping Myopathic and Neurogenic Findings

Por Agrawal, Pankaj B., Joshi, Mugdha, Marinakis, Nicholas S., Schmitz-Abe, Klaus, Ciarlini, Pedro D. S. C., Sargent, Jane C., Markianos, Kyriacos, De Girolami, Umberto, Chad, David A., Beggs, Alan H.
Publicado no JAMA Neurol (2014)

A cryptic subgroup of Anopheles gambiae is highly susceptible to human malaria parasites

Por Riehle, Michelle M., Guelbeogo, Wamdaogo M., Gneme, Awa, Eiglmeier, Karin, Holm, Inge, Bischoff, Emmanuel, Garnier, Thierry, Snyder, Gregory M., Li, Xuanzhong, Markianos, Kyriacos, Sagnon, N’Fale, Vernick, Kenneth D.
Publicado em 2011

Lack of Association of the Serotonin Transporter Polymorphism With the Sudden Infant Death Syndrome in the San Diego Dataset

Por Paterson, David S., Rivera, Keith D., Broadbelt, Kevin G., Trachtenberg, Felicia L., Belliveau, Richard A., Holm, Ingrid A., Haas, Elisabeth A., Stanley, Christina, Krous, Henry F., Kinney, Hannah C., Markianos, Kyriacos
Publicado em 2010

Comparative RNA Editing in Autistic and Neurotypical Cerebella

Por Eran, Alal, Li, Jin Billy, Vatalaro, Kayla, McCarthy, Jillian, Rahimov, Fedik, Collins, Christin, Markianos, Kyriacos, Margulies, David M., Brown, Emery N., Calvo, Sarah E., Kohane, Isaac S., Kunkel, Louis M.
Publicado em 2012

RINGED SIDEROBLASTS IN β-THALASSEMIA

Por Cattivelli, Kim, Campagna, Dean R., Schmitz-Abe, Klaus, Heeney, Matthew M., Yaish, Hassan M., Caruso Brown, Amy E., Kearney, Susan, Walkovich, Kelly, Markianos, Kyriacos, Fleming, Mark D., Neufeld, Ellis J.
Publicado no Pediatr Blood Cancer (2016)

Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)

Por Finberg, Karin E, Heeney, Matthew M, Campagna, Dean R, Aydınok, Yeşim, Pearson, Howard A, Hartman, Kip R, Mayo, Mary M, Samuel, Stewart M, Strouse, John J, Markianos, Kyriacos, Andrews, Nancy C, Fleming, Mark D
Publicado em 2008

Mutations in the substrate binding glycine-rich loop of the mitochondrial processing peptidase-α protein (PMPCA) cause a severe mitochondrial disease

Por Joshi, Mugdha, Anselm, Irina, Shi, Jiahai, Bale, Tejus A., Towne, Meghan, Schmitz-Abe, Klaus, Crowley, Laura, Giani, Felix C., Kazerounian, Shideh, Markianos, Kyriacos, Lidov, Hart G., Folkerth, Rebecca, Sankaran, Vijay G., Agrawal, Pankaj B.
Publicado no Cold Spring Harb Mol Case Stud (2016)

LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure

Por Riley, Lisa G., Rudinger-Thirion, Joëlle, Schmitz-Abe, Klaus, Thorburn, David R., Davis, Ryan L., Teo, Juliana, Arbuckle, Susan, Cooper, Sandra T., Campagna, Dean R., Frugier, Magali, Markianos, Kyriacos, Sue, Carolyn M., Fleming, Mark D., Christodoulou, John
Publicado no JIMD Rep (2015)

Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae

Por Redmond, Seth N., Eiglmeier, Karin, Mitri, Christian, Markianos, Kyriacos, Guelbeogo, Wamdaogo M., Gneme, Awa, Isaacs, Alison T., Coulibaly, Boubacar, Brito-Fravallo, Emma, Maslen, Gareth, Mead, Daniel, Niare, Oumou, Traore, Sekou F., Sagnon, N’Fale, Kwiatkowski, Dominic, Riehle, Michelle M., Vernick, Kenneth D.
Publicado no BMC Genomics (2015)

Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

Por Schmitz-Abe, Klaus, Sanchez-Schmitz, Guzman, Doan, Ryan N., Hill, R. Sean, Chahrour, Maria H., Mehta, Bhaven K., Servattalab, Sarah, Ataman, Bulent, Lam, Anh-Thu N., Morrow, Eric M., Greenberg, Michael E., Yu, Timothy W., Walsh, Christopher A., Markianos, Kyriacos
Publicado no Sci Rep (2020)

Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy

Por Ceyhan-Birsoy, Ozge, Agrawal, Pankaj B., Hidalgo, Carlos, Schmitz-Abe, Klaus, DeChene, Elizabeth T., Swanson, Lindsay C., Soemedi, Rachel, Vasli, Nasim, Iannaccone, Susan T., Shieh, Perry B., Shur, Natasha, Dennison, Jane M., Lawlor, Michael W., Laporte, Jocelyn, Markianos, Kyriacos, Fairbrother, William G., Granzier, Henk, Beggs, Alan H.
Publicado em 2013