Efficient Multipoint Linkage Analysis through Reduction of Inheritance Space

Tekijä Markianos, Kyriacos, Daly, Mark J., Kruglyak, Leonid
Julkaistu 2001

No Bias in Linkage Analysis

Tekijä Abecasis, Goncalo, Cox, Nancy, Daly, Mark J., Kruglyak, Leonid, Laird, Nan, Markianos, Kyriacos, Patterson, Nick
Julkaistu 2004

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

Tekijä Riehle, Michelle M, Markianos, Kyriacos, Lambrechts, Louis, Xia, Ai, Sharakhov, Igor, Koella, Jacob C, Vernick, Kenneth D
Julkaistu 2007

Sequence-Based Linkage Analysis

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

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

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

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

Tekijä Mitri, Christian, Markianos, Kyriacos, Guelbeogo, Wamdaogo M., Bischoff, Emmanuel, Gneme, Awa, Eiglmeier, Karin, Holm, Inge, Sagnon, N’Fale, Vernick, Kenneth D., Riehle, Michelle M.
Julkaisussa Malar J (2015)

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

Tekijä Markianos, Kyriacos, Bischoff, Emmanuel, Mitri, Christian, Guelbeogo, Wamdaogo M., Gneme, Awa, Eiglmeier, Karin, Holm, Inge, Sagnon, N’Fale, Vernick, Kenneth D., Riehle, Michelle M.
Julkaisussa PLoS One (2016)

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

Tekijä 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.
Julkaistu 2009

Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants

Tekijä 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.
Julkaisussa JIMD Rep (2016)

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

Tekijä 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.
Julkaisussa JAMA Neurol (2014)

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

Tekijä 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.
Julkaistu 2011

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

Tekijä 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
Julkaistu 2010

Comparative RNA Editing in Autistic and Neurotypical Cerebella

Tekijä 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.
Julkaistu 2012

RINGED SIDEROBLASTS IN β-THALASSEMIA

Tekijä 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.
Julkaisussa Pediatr Blood Cancer (2016)

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

Tekijä 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
Julkaistu 2008

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

Tekijä 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.
Julkaisussa Cold Spring Harb Mol Case Stud (2016)

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

Tekijä 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
Julkaisussa JIMD Rep (2015)

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

Tekijä 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.
Julkaisussa BMC Genomics (2015)

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

Tekijä 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
Julkaisussa Sci Rep (2020)

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

Tekijä 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.
Julkaistu 2013