Human-specific transcriptional regulation of CNS development genes by FOXP2
Winden, Kellen, Geschwind, Daniel H, Preuss, Todd M, Jonsson, Zophonias O, Coppola, Giovanni, Gao, Fuying, Konopka, Genevieve, Wohlschlegel, James A, Bomar, Jamee M, Peng, Sophia
Published in Nature (London) (12.11.2009)
Published in Nature (London) (12.11.2009)
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Journal Article
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
Alarcón, Maricela, Abrahams, Brett S., Stone, Jennifer L., Duvall, Jacqueline A., Perederiy, Julia V., Bomar, Jamee M., Sebat, Jonathan, Wigler, Michael, Martin, Christa L., Ledbetter, David H., Nelson, Stanley F., Cantor, Rita M., Geschwind, Daniel H.
Published in American journal of human genetics (01.01.2008)
Published in American journal of human genetics (01.01.2008)
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Journal Article
Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain
Spiteri, Elizabeth, Konopka, Genevieve, Coppola, Giovanni, Bomar, Jamee, Oldham, Michael, Ou, Jing, Vernes, Sonja C., Fisher, Simon E., Ren, Bing, Geschwind, Daniel H.
Published in American journal of human genetics (01.12.2007)
Published in American journal of human genetics (01.12.2007)
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Fate of cajal-retzius neurons in the postnatal mouse neocortex
Chowdhury, Tara G, Jimenez, Jessica C, Bomar, Jamee M, Cruz-Martin, Alberto, Cantle, Jeffrey P, Portera-Cailliau, Carlos
Published in Frontiers in neuroanatomy (03.03.2010)
Published in Frontiers in neuroanatomy (03.03.2010)
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Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse
Burmeister, Margit, Bomar, Jamee M, Benke, Paul J, Slattery, Eric L, Puttagunta, Radhika, Taylor, Larry P, Seong, Eunju, Nystuen, Arne, Chen, Weidong, Albin, Roger L, Patel, Paresh D, Kittles, Rick A, Sheffield, Val C
Published in Nature genetics (01.11.2003)
Published in Nature genetics (01.11.2003)
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Characterization of a mutagenic B1 retrotransposon insertion in the jittery mouse
Gilbert, Nicolas, Bomar, Jamee M., Burmeister, Margit, Moran, John V.
Published in Human mutation (01.07.2004)
Published in Human mutation (01.07.2004)
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X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Jenkinson, Andrew, Varian, Jennifer, Shoubridge, Cheryl, Vandeleur, Lucianne, Shepherd, Rebecca, Hynes, Kim, Shaw, Marie, Gusella, James F, Teague, John, Edkins, Sarah, Dicks, Ed, Dibbens, Leanne M, Haan, Eric, Gécz, Jozef, Halliday, Kelly, Lerman-Sagie, Tally, Sutton, Edwina, Corbett, Mark, Wray, Paul, Bomar, Jamee, Stevens, Claire, Scheffer, Ingrid E, Barthorpe, Syd, Butler, Adam, Tarpey, Patrick S, Jones, David, Bayly, Marta A, Madison, Mark, West, Sofie, Lev, Dorit, Stratton, Michael R, Neufeld, Miriam Y, Korczyn, Amos D, Tofts, Calli, Futreal, P Andrew, Turner, Samantha J, Kim, Hyung-Goo, Berkovic, Samuel F, Buck, Gemma, O'Meara, Sarah, Friend, Kathryn, Kivity, Sara, Afawi, Zaid, Mironenko, Tatiana, McKee, Shane, Cole, Jennifer, Lee, Rebecca, Geschwind, Daniel H, Widaa, Sara, Ryan, Stephen, Smith, Raffaella, Sutherland, Grant R, Menzies, Andrew, Mulley, John C, Mazarib, Aziz, Derry, Christopher P, Thomas, Paul
Published in Nature genetics (01.06.2008)
Published in Nature genetics (01.06.2008)
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Human-specific transcriptional regulation of CANS development genes by FOXP2
KONOPKA, Genevieve, BOMAR, Jamee M, WINDEN, Kellen, COPPOLA, Giovanni, JONSSON, Zophonias O, FUYING GAO, SOPHIA PENG, PREUSS, Todd M, WOHLSCHLEGEL, James A, GESCHWIND, Daniel H
Published in Nature (London) (2009)
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Published in Nature (London) (2009)
Journal Article
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene. Commentary
STEPHAN, Dietrich A, ALARCON, Maricela, LEDBETTER, David H, NELSON, Stanley F, CANTOR, Rita M, GESCHWIND, Daniel H, ABRAHAMS, Brett S, STONE, Jennifer L, DUVALL, Jacqueline A, PEREDERIY, Julia V, BOMAR, Jamee M, SEBAT, Jonathan, WIGLER, Michael, MARTIN, Christa L
Published in American journal of human genetics (2008)
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Published in American journal of human genetics (2008)
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