Association and mutation analyses of 16p11.2 autism candidate genes
Kumar, Ravinesh A, Marshall, Christian R, Badner, Judith A, Babatz, Timothy D, Mukamel, Zohar, Aldinger, Kimberly A, Sudi, Jyotsna, Brune, Camille W, Goh, Gerald, Karamohamed, Samer, Sutcliffe, James S, Cook, Edwin H, Geschwind, Daniel H, Dobyns, William B, Scherer, Stephen W, Christian, Susan L
Published in PloS one (26.02.2009)
Published in PloS one (26.02.2009)
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Copy number and sequence variants implicate APBA2 as an autism candidate gene
Babatz, Timothy D, Kumar, Ravinesh A, Sudi, Jyotsna, Dobyns, William B, Christian, Susan L
Published in Autism research (01.12.2009)
Published in Autism research (01.12.2009)
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Site specificity determinants for prelamin A cleavage by the zinc metalloprotease ZMPSTE24
Babatz, Timothy D., Spear, Eric D., Xu, Wenxin, Sun, Olivia L., Nie, Laiyin, Carpenter, Elisabeth P., Michaelis, Susan
Published in The Journal of biological chemistry (01.01.2021)
Published in The Journal of biological chemistry (01.01.2021)
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TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins
Kumar, Ravinesh A., Pilz, Daniela T., Babatz, Timothy D., Cushion, Thomas D., Harvey, Kirsten, Topf, Maya, Yates, Laura, Robb, Stephanie, Uyanik, Gökhan, Mancini, Gracia M.S., Rees, Mark I., Harvey, Robert J., Dobyns, William B.
Published in Human molecular genetics (15.07.2010)
Published in Human molecular genetics (15.07.2010)
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Functional impact of the human mobilome
Babatz, Timothy D, Burns, Kathleen H
Published in Current opinion in genetics & development (01.06.2013)
Published in Current opinion in genetics & development (01.06.2013)
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A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism
Kumar, Ravinesh A, Sudi, Jyotsna, Babatz, Timothy D, Brune, Camille W, Oswald, Donald, Yen, Mayon, Nowak, Norma J, Cook, Edwin H, Christian, Susan L, Dobyns, William B
Published in Journal of medical genetics (01.02.2010)
Published in Journal of medical genetics (01.02.2010)
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