Incorporating prior biological information in linkage studies increases power and limits multiple testing

Autor Lantieri, Francesca, Rydbeck, Halfdan, Griseri, Paola, Ceccherini, Isabella, Devoto, Marcella
Vydáno 2007

Association of a Polymorphic Variant of the Adiponectin Gene with Insulin Resistance in African Americans

Autor Specchia, Claudia, Scott, Kathryn, Fortina, Paolo, Devoto, Marcella, Falkner, Bonita
Vydáno v Clin Transl Sci (2008)

An Exploratory Association Analysis of the Insulin Gene Region With Diabetes Mellitus in Two Dog Breeds

Autor Hess, Rebecka, Henthorn, Paula, Devoto, Marcella, Wang, Fan, Feng, Rui
Vydáno v J Hered (2019)

Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study

Autor Lantieri, Francesca, Jhun, Min A, Park, Jungsun, Park, Taesung, Devoto, Marcella
Vydáno 2009

Novel ZBTB24 mutation associated with immunodeficiency, centromere instability, and facial anomalies type 2 syndrome identified in a patient with very early onset inflammatory bowe...

Autor Conrad, Máire A., Dawany, Noor, Sullivan, Kathleen E., Devoto, Marcella, Kelsen, Judith R.
Vydáno v Inflamm Bowel Dis (2017)

Genome-Wide Linkage Analysis to Identify Genetic Modifiers of ALK Mutation Penetrance in Familial Neuroblastoma

Autor Devoto, Marcella, Specchia, Claudia, Laudenslager, Marci, Longo, Luca, Hakonarson, Hakon, Maris, John, Mossé, Yael
Vydáno 2011

Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota

Autor Nallasamy, Sudha, Paluru, Prasuna C., Devoto, Marcella, Wasserman, Nora F., Zhou, Jie, Young, Terri L.
Vydáno 2007

The Otto Aufranc Award: Identification of a 4 Mb Region on Chromosome 17q21 Linked to Developmental Dysplasia of the Hip in One 18-member, Multigeneration Family

Autor Feldman, George, Dalsey, Chelsea, Fertala, Kasia, Azimi, David, Fortina, Paolo, Devoto, Marcella, Pacifici, Maurizio, Parvizi, Javad
Vydáno 2009

Replication of neuroblastoma SNP association at the BARD1 locus in African-Americans

Autor Latorre, Valeria, Diskin, Sharon J., Diamond, Maura A., Zhang, Haitao, Hakonarson, Hakon, Maris, John M., Devoto, Marcella
Vydáno 2012

Variants of ST8SIA1 Are Associated with Risk of Developing Multiple Sclerosis

Autor Husain, Seema, Yildirim-Toruner, Cagri, Rubio, Justin P., Field, Judith, Schwalb, Marvin, Cook, Stuart, Devoto, Marcella, Vitale, Emilia
Vydáno 2008

Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion

Autor Danjou, Fabrice, Anni, Franco, Perseu, Lucia, Satta, Stefania, Dessì, Carlo, Lai, Maria Eliana, Fortina, Paolo, Devoto, Marcella, Galanello, Renzo
Vydáno 2012

Exome Sequencing in Individuals with Isolated Biliary Atresia

Autor Rajagopalan, Ramakrishnan, Tsai, Ellen A., Grochowski, Christopher M., Kelly, Susan M., Loomes, Kathleen M., Spinner, Nancy B., Devoto, Marcella
Vydáno v Sci Rep (2020)

Precocious Sister Chromatid Separation (PSCS) in Cornelia de Lange Syndrome

Autor Kaur, Maninder, DeScipio, Cheryl, McCallum, Jennifer, Yaeger, Dinah, Devoto, Marcella, Jackson, Laird G., Spinner, Nancy B., Krantz, Ian D.
Vydáno 2005

The Unique Disease Course of Children with Very Early onset-Inflammatory Bowel Disease

Autor Kelsen, Judith R, Conrad, Maire A, Dawany, Noor, Patel, Trusha, Shraim, Rawan, Merz, Audrey, Maurer, Kelly, Sullivan, Kathleen E, Devoto, Marcella
Vydáno v Inflamm Bowel Dis (2020)

A Rare Haplotype of the RET Proto-Oncogene Is a Risk-Modifying Allele in Hirschsprung Disease

Autor Griseri, Paola, Pesce, Barbara, Patrone, Giovanna, Osinga, Jan, Puppo, Francesca, Sancandi, Monica, Hofstra, Robert, Romeo, Giovanni, Ravazzolo, Roberto, Devoto, Marcella, Ceccherini, Isabella
Vydáno 2002

Heterozygous Deletion of FOXA2 Segregates with Disease in a Family with Heterotaxy, Panhypopituitarism, and Biliary Atresia

Autor Tsai, Ellen A., Grochowski, Christopher M., Falsey, Alexandra M., Rajagopalan, Ramakrishnan, Wendel, Danielle, Devoto, Marcella, Krantz, Ian D., Loomes, Kathleen M., Spinner, Nancy B.
Vydáno v Hum Mutat (2015)

Evidence From Human and Zebrafish That GPC1 Is a Biliary Atresia Susceptibility Gene

Autor Cui, Shuang, Leyva-Vega, Melissa, Tsai, Ellen A., Eauclaire, Steven F., Glessner, Joseph T., Hakonarson, Hakon, Devoto, Marcella, Haber, Barbara A., Spinner, Nancy B., Matthews, Randolph P.
Vydáno 2013

Exclusion of Linkage to the CDL1 Gene Region on Chromosome 3q26.3 in Some Familial Cases of Cornelia de Lange Syndrome

Autor Krantz, Ian D., Tonkin, Emma, Smith, Melanie, Devoto, Marcella, Bottani, Armand, Simpson, Claire, Hofreiter, Mary, Abraham, Vinod, Jukofsky, Lori, Conti, Brian P., Strachan, Tom, Jackson, Laird
Vydáno v Am J Med Genet (2001)

IQ and Hemizygosity for the Val(158)Met Functional Polymorphism of COMT in 22q11DS

Autor Franconi, Colleen P., McDonald-McGinn, Donna, H.Zackai, Elaine, McNamara, Meghan A., Salmons, Harold, Moss, Edward, Gur, Raquel E., Devoto, Marcella, Emanuel, Beverly S.
Vydáno v Am J Med Genet B Neuropsychiatr Genet (2016)

Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia

Autor Tsai, Ellen A., Grochowski, Christopher M., Loomes, Kathleen M., Bessho, Kazuhiko, Hakonarson, Hakon, Bezerra, Jorge A., Russo, Pierre A., Haber, Barbara A., Spinner, Nancy B., Devoto, Marcella
Vydáno 2013