Kathleen Millen - Publications

Affiliations: 
University of Chicago, Chicago, IL 
 University of Washington, Seattle, Seattle, WA 
 Seattle Children's Rese 
Area:
developmental neurogenetics

89 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Roy A, Millen KJ, Kapur RP. Hippocampal granule cell dispersion: a non-specific finding in pediatric patients with no history of seizures. Acta Neuropathologica Communications. 8: 54. PMID 32317027 DOI: 10.1186/s40478-020-00928-3  1
2020 Roy A, Deng M, Aldinger KA, Glass IA, Millen KJ. Laser Capture Micro-dissection (LCM) of Neonatal Mouse Forebrain for RNA Isolation. Bio-Protocol. 10. PMID 32190713  1
2019 Chizhikov VV, Iskusnykh IY, Steshina EY, Fattakhov N, Lindgren AG, Shetty AS, Roy A, Tole S, Millen KJ. Early dorsomedial tissue interactions regulate gyrification of distal neocortex. Nature Communications. 10: 5192. PMID 31729356 DOI: 10.1038/s41467-019-12913-z  1
2019 Haldipur P, Aldinger KA, Bernardo S, Deng M, Timms AE, Overman LM, Winter C, Lisgo SN, Razavi F, Silvestri E, Manganaro L, Adle-Biasette H, Guilmiot F, Russo R, Kidron D, ... ... Millen KJ, et al. Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum. Science (New York, N.Y.). 366: 454-460. PMID 31624095 DOI: 10.1126/science.aax7526  1
2019 Aldinger KA, Timms AE, Thomson Z, Mirzaa GM, Bennett JT, Rosenberg AB, Roco CM, Hirano M, Abidi F, Haldipur P, Cheng CV, Collins S, Park K, Zeiger J, Overmann LM, ... ... Millen KJ, et al. Redefining the Etiologic Landscape of Cerebellar Malformations. American Journal of Human Genetics. PMID 31474318 DOI: 10.1016/j.ajhg.2019.07.019  1
2019 Roy A, Murphy RM, Deng M, MacDonald JW, Bammler TK, Aldinger KA, Glass IA, Millen KJ. PI3K-Yap activity drives cortical gyrification and hydrocephalus in mice. Elife. 8. PMID 31094678 DOI: 10.7554/eLife.45961  1
2018 Haldipur P, Dang D, Millen KJ. Embryology. Handbook of Clinical Neurology. 154: 29-44. PMID 29903446 DOI: 10.1016/B978-0-444-63956-1.00002-3  1
2018 Kridsada K, Niu J, Haldipur P, Wang Z, Ding L, Li JJ, Lindgren AG, Herrera E, Thomas GM, Chizhikov VV, Millen KJ, Luo W. Roof Plate-Derived Radial Glial-like Cells Support Developmental Growth of Rapidly Adapting Mechanoreceptor Ascending Axons. Cell Reports. 23: 2928-2941. PMID 29874580 DOI: 10.1016/j.celrep.2018.05.025  1
2018 Haldipur P, Millen KJ. What cerebellar malformations tell us about cerebellar development. Neuroscience Letters. PMID 29802918 DOI: 10.1016/j.neulet.2018.05.032  1
2017 Haldipur P, Dang D, Aldinger KA, Janson OK, Guimiot F, Adle-Biasette H, Dobyns WB, Siebert JR, Russo R, Millen KJ. Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms. Elife. 6. PMID 28092268 DOI: 10.7554/eLife.20898  1
2016 Di Donato N, Jean YY, Maga AM, Krewson BD, Shupp AB, Avrutsky MI, Roy A, Collins S, Olds C, Willert RA, Czaja AM, Johnson R, Stover JA, Gottlieb S, Bartholdi D, ... ... Millen KJ, et al. Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant. American Journal of Human Genetics. PMID 27773430 DOI: 10.1016/j.ajhg.2016.09.010  1
2016 Lin CY, Erkek S, Tong Y, Yin L, Federation AJ, Zapatka M, Haldipur P, Kawauchi D, Risch T, Warnatz HJ, Worst BC, Ju B, Orr BA, Zeid R, Polaski DR, ... ... Millen KJ, et al. Active medulloblastoma enhancers reveal subgroup-specific cellular origins. Nature. PMID 26814967 DOI: 10.1038/nature16546  1
2015 Roy A, Skibo J, Kalume F, Ni J, Rankin S, Lu Y, Dobyns WB, Mills GB, Zhao JJ, Baker SJ, Millen KJ. Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy. Elife. 4. PMID 26633882 DOI: 10.7554/eLife.12703  1
2015 Roy A, Ni J, Skibo J, Rankin S, Dobyns WB, Kalume F, Baker SJ, Zhao J, Millen KJ. Modeling human PIK3CA-related congenital brain overgrowth and epilepsy in mice. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 46. PMID 26531452 DOI: 10.1016/j.ijdevneu.2015.04.131  1
2015 Haldipur P, Gillies G, Janson OK, Chizhikov VV, Millen KJ. Mesenchymal Foxc1 non-autonomously controls cerebellar development through SDF1α-CXCR4 maintenance of radial glial cells. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 34. PMID 26531419 DOI: 10.1016/j.ijdevneu.2015.04.097  1
2015 Leto K, Arancillo M, Becker EB, Buffo A, Chiang C, Ding B, Dobyns WB, Dusart I, Haldipur P, Hatten ME, Hoshino M, Joyner AL, Kano M, Kilpatrick DL, Koibuchi N, ... ... Millen KJ, et al. Consensus Paper: Cerebellar Development. Cerebellum (London, England). PMID 26439486 DOI: 10.1007/s12311-015-0724-2  1
2015 Comer JD, Pan FC, Willet SG, Haldipur P, Millen KJ, Wright CV, Kaltschmidt JA. Sensory and spinal inhibitory dorsal midline crossing is independent of Robo3. Frontiers in Neural Circuits. 9: 36. PMID 26257608 DOI: 10.3389/fncir.2015.00036  1
2015 Tully HM, Ishak GE, Rue TC, Dempsey JC, Browd SR, Millen KJ, Doherty D, Dobyns WB. Two Hundred Thirty-Six Children With Developmental Hydrocephalus: Causes and Clinical Consequences. Journal of Child Neurology. PMID 26184484 DOI: 10.1177/0883073815592222  1
2015 Shih EK, Sekerková G, Ohtsuki G, Aldinger KA, Chizhikov VV, Hansel C, Mugnaini E, Millen KJ. The Spontaneous Ataxic Mouse Mutant Tippy is Characterized by a Novel Purkinje Cell Morphogenesis and Degeneration Phenotype. Cerebellum (London, England). 14: 292-307. PMID 25626522 DOI: 10.1007/s12311-014-0640-x  1
2014 Haldipur P, Gillies GS, Janson OK, Chizhikov VV, Mithal DS, Miller RJ, Millen KJ. Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth. Elife. 3. PMID 25513817 DOI: 10.7554/eLife.03962  1
2014 French CR, Seshadri S, Destefano AL, Fornage M, Arnold CR, Gage PJ, Skarie JM, Dobyns WB, Millen KJ, Liu T, Dietz W, Kume T, Hofker M, Emery DJ, Childs SJ, et al. Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease. The Journal of Clinical Investigation. 124: 4877-81. PMID 25250569 DOI: 10.1172/JCI75109  1
2014 Chervenak AP, Bank LM, Thomsen N, Glanville-Jones HC, Jonathan S, Millen KJ, Arkell RM, Barald KF. The role of Zic genes in inner ear development in the mouse: Exploring mutant mouse phenotypes. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 243: 1487-98. PMID 25178196 DOI: 10.1002/dvdy.24186  1
2014 Millen KJ, Steshina EY, Iskusnykh IY, Chizhikov VV. Transformation of the cerebellum into more ventral brainstem fates causes cerebellar agenesis in the absence of Ptf1a function. Proceedings of the National Academy of Sciences of the United States of America. 111: E1777-86. PMID 24733890 DOI: 10.1073/pnas.1315024111  1
2014 Mirzaa GM, Millen KJ, Barkovich AJ, Dobyns WB, Paciorkowski AR. The Developmental Brain Disorders Database (DBDB): a curated neurogenetics knowledge base with clinical and research applications. American Journal of Medical Genetics. Part A. 164: 1503-11. PMID 24700709 DOI: 10.1002/ajmg.a.36517  1
2014 Traudt CM, McPherson RJ, Studholme C, Millen KJ, Juul SE. Systemic glycerol decreases neonatal rabbit brain and cerebellar growth independent of intraventricular hemorrhage. Pediatric Research. 75: 389-94. PMID 24346111 DOI: 10.1038/pr.2013.236  1
2014 Sillitoe RV, George-Jones NA, Millen KJ, Hawkes R. Purkinje cell compartmentalization in the cerebellum of the spontaneous mutant mouse dreher. Brain Structure & Function. 219: 35-47. PMID 23160833 DOI: 10.1007/s00429-012-0482-6  1
2013 Haldipur P, Millen KJ. Deficits in early neural tube identity found in CHARGE syndrome. Elife. 2: e01873. PMID 24368735 DOI: 10.7554/eLife.01873  1
2013 Lehoczky JA, Thomas PE, Patrie KM, Owens KM, Villarreal LM, Galbraith K, Washburn J, Johnson CN, Gavino B, Borowsky AD, Millen KJ, Wakenight P, Law W, Van Keuren ML, Gavrilina G, et al. A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice. Plos Genetics. 9: e1003967. PMID 24339789 DOI: 10.1371/journal.pgen.1003967  1
2013 Sajan SA, Fernandez L, Nieh SE, Rider E, Bukshpun P, Wakahiro M, Christian SL, Rivière JB, Sullivan CT, Sudi J, Herriges MJ, Paciorkowski AR, Barkovich AJ, Glessner JT, Millen KJ, et al. Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria. Plos Genetics. 9: e1003823. PMID 24098143 DOI: 10.1371/journal.pgen.1003823  1
2013 Darbro BW, Mahajan VB, Gakhar L, Skeie JM, Campbell E, Wu S, Bing X, Millen KJ, Dobyns WB, Kessler JA, Jalali A, Cremer J, Segre A, Manak JR, Aldinger KA, et al. Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles. Human Mutation. 34: 1075-9. PMID 23674478 DOI: 10.1002/humu.22351  1
2013 Traka M, Millen KJ, Collins D, Elbaz B, Kidd GJ, Gomez CM, Popko B. WDR81 is necessary for purkinje and photoreceptor cell survival. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 6834-44. PMID 23595742 DOI: 10.1523/JNEUROSCI.2394-12.2013  1
2013 Doherty D, Millen KJ, Barkovich AJ. Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics. The Lancet. Neurology. 12: 381-93. PMID 23518331 DOI: 10.1016/S1474-4422(13)70024-3  1
2013 Aldinger KA, Kogan J, Kimonis V, Fernandez B, Horn D, Klopocki E, Chung B, Toutain A, Weksberg R, Millen KJ, Barkovich AJ, Dobyns WB. Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion. American Journal of Medical Genetics. Part A. 161: 131-6. PMID 23225497 DOI: 10.1002/ajmg.a.35700  1
2013 Chizhikov VV, Millen KJ. Neurogenesis in the Cerebellum Comprehensive Developmental Neuroscience: Patterning and Cell Type Specification in the Developing Cns and Pns. 417-434. DOI: 10.1016/B978-0-12-397265-1.00067-8  1
2012 Tully HM, Dempsey JC, Ishak GE, Adam MP, Curry CJ, Sanchez-Lara P, Hunter A, Gripp KW, Allanson J, Cunniff C, Glass I, Millen KJ, Doherty D, Dobyns WB. Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsis. American Journal of Medical Genetics. Part A. 158: 2393-406. PMID 22965664 DOI: 10.1002/ajmg.a.35561  1
2012 Nieman BJ, Blank MC, Roman BB, Henkelman RM, Millen KJ. If the skull fits: magnetic resonance imaging and microcomputed tomography for combined analysis of brain and skull phenotypes in the mouse. Physiological Genomics. 44: 992-1002. PMID 22947655 DOI: 10.1152/physiolgenomics.00093.2012  1
2012 Yusuf D, Butland SL, Swanson MI, Bolotin E, Ticoll A, Cheung WA, Zhang XY, Dickman CT, Fulton DL, Lim JS, Schnabl JM, Ramos OH, Vasseur-Cognet M, de Leeuw CN, Simpson EM, ... ... Millen KJ, et al. The transcription factor encyclopedia. Genome Biology. 13: R24. PMID 22458515 DOI: 10.1186/gb-2012-13-3-r24  0.24
2012 Ishak GE, Dempsey JC, Shaw DW, Tully H, Adam MP, Sanchez-Lara PA, Glass I, Rue TC, Millen KJ, Dobyns WB, Doherty D. Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity. Brain : a Journal of Neurology. 135: 1370-86. PMID 22451504 DOI: 10.1093/brain/aws065  1
2012 Fatemi SH, Aldinger KA, Ashwood P, Bauman ML, Blaha CD, Blatt GJ, Chauhan A, Chauhan V, Dager SR, Dickson PE, Estes AM, Goldowitz D, Heck DH, Kemper TL, King BH, ... ... Millen KJ, et al. Consensus paper: pathological role of the cerebellum in autism. Cerebellum (London, England). 11: 777-807. PMID 22370873 DOI: 10.1007/s12311-012-0355-9  1
2011 Doherty D, Millen KJ. Wormless without wingless. Nature Medicine. 17: 663-5. PMID 21647144 DOI: 10.1038/nm0611-663  1
2011 Chung SH, Marzban H, Aldinger K, Dixit R, Millen K, Schuurmans C, Hawkes R. Zac1 plays a key role in the development of specific neuronal subsets in the mouse cerebellum. Neural Development. 6: 25. PMID 21592321 DOI: 10.1186/1749-8104-6-25  1
2011 Blank MC, Grinberg I, Aryee E, Laliberte C, Chizhikov VV, Henkelman RM, Millen KJ. Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis. Development (Cambridge, England). 138: 1207-16. PMID 21307096 DOI: 10.1242/dev.054114  1
2010 Swanson DJ, Steshina EY, Wakenight P, Aldinger KA, Goldowitz D, Millen KJ, Chizhikov VV. Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele. The European Journal of Neuroscience. 32: 707-16. PMID 20722722 DOI: 10.1111/j.1460-9568.2010.07330.x  1
2010 Waite A, Somer M, O'Driscoll M, Millen K, Manson FD, Chandler KE. Cerebellar hypoplasia and Cohen syndrome: a confirmed association. American Journal of Medical Genetics. Part A. 152: 2390-3. PMID 20683995 DOI: 10.1002/ajmg.a.33569  1
2010 Chizhikov VV, Lindgren AG, Mishima Y, Roberts RW, Aldinger KA, Miesegaes GR, Currle DS, Monuki ES, Millen KJ. Lmx1a regulates fates and location of cells originating from the cerebellar rhombic lip and telencephalic cortical hem. Proceedings of the National Academy of Sciences of the United States of America. 107: 10725-30. PMID 20498066 DOI: 10.1073/pnas.0910786107  1
2010 Sajan SA, Waimey KE, Millen KJ. Novel approaches to studying the genetic basis of cerebellar development. Cerebellum (London, England). 9: 272-83. PMID 20387026 DOI: 10.1007/s12311-010-0169-6  1
2010 Barkovich AJ, Dobyns WB, Millen KJ. Letter to the editor: Reply: Sagging and swelling of the midbrain suggest spontaneous intracranial hypotension rather than a malformation Brain. 133: e149. DOI: 10.1093/brain/awq031  1
2009 Barkovich AJ, Millen KJ, Dobyns WB. A developmental and genetic classification for midbrain-hindbrain malformations. Brain : a Journal of Neurology. 132: 3199-230. PMID 19933510 DOI: 10.1093/brain/awp247  1
2009 Iossifov I, Rodriguez-Esteban R, Mayzus I, Millen KJ, Rzhetsky A. Looking at cerebellar malformations through text-mined interactomes of mice and humans. Plos Computational Biology. 5: e1000559. PMID 19893633 DOI: 10.1371/journal.pcbi.1000559  1
2009 Horng S, Kreiman G, Ellsworth C, Page D, Blank M, Millen K, Sur M. Differential gene expression in the developing lateral geniculate nucleus and medial geniculate nucleus reveals novel roles for Zic4 and Foxp2 in visual and auditory pathway development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 13672-83. PMID 19864579 DOI: 10.1523/JNEUROSCI.2127-09.2009  1
2009 Aldinger KA, Elsen GE, Prince VE, Millen KJ. Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain. Seminars in Pediatric Neurology. 16: 155-63. PMID 19778712 DOI: 10.1016/j.spen.2009.06.003  1
2009 Mishima Y, Lindgren AG, Chizhikov VV, Johnson RL, Millen KJ. Overlapping function of Lmx1a and Lmx1b in anterior hindbrain roof plate formation and cerebellar growth. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 11377-84. PMID 19741143 DOI: 10.1523/JNEUROSCI.0969-09.2009  1
2009 Aldinger KA, Lehmann OJ, Hudgins L, Chizhikov VV, Bassuk AG, Ades LC, Krantz ID, Dobyns WB, Millen KJ. FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation. Nature Genetics. 41: 1037-42. PMID 19668217 DOI: 10.1038/ng.422  1
2009 Koo SK, Hill JK, Hwang CH, Lin ZS, Millen KJ, Wu DK. Lmx1a maintains proper neurogenic, sensory, and non-sensory domains in the mammalian inner ear. Developmental Biology. 333: 14-25. PMID 19540218 DOI: 10.1016/j.ydbio.2009.06.016  1
2009 Aldinger KA, Sokoloff G, Rosenberg DM, Palmer AA, Millen KJ. Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies. Plos One. 4: e4729. PMID 19266100 DOI: 10.1371/journal.pone.0004729  1
2008 Nichols DH, Pauley S, Jahan I, Beisel KW, Millen KJ, Fritzsch B. Lmx1a is required for segregation of sensory epithelia and normal ear histogenesis and morphogenesis. Cell and Tissue Research. 334: 339-58. PMID 18985389 DOI: 10.1007/s00441-008-0709-2  1
2008 Millen KJ, Gleeson JG. Cerebellar development and disease. Current Opinion in Neurobiology. 18: 12-9. PMID 18513948 DOI: 10.1016/j.conb.2008.05.010  1
2008 Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, ... ... Millen KJ, et al. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics. 123: 237-45. PMID 18204864 DOI: 10.1007/s00439-008-0467-y  1
2008 Elsen GE, Choi LY, Millen KJ, Grinblat Y, Prince VE. Zic1 and Zic4 regulate zebrafish roof plate specification and hindbrain ventricle morphogenesis. Developmental Biology. 314: 376-92. PMID 18191121 DOI: 10.1016/j.ydbio.2007.12.006  1
2007 Blank MC, Chizhikov V, Millen KJ. In ovo electroporations of HH stage 10 chicken embryos. Journal of Visualized Experiments : Jove. 408. PMID 18989448 DOI: 10.3791/408  1
2007 Millen KJ. Understanding cerebellar pattern formation. Journal of Visualized Experiments : Jove. 407. PMID 18989447 DOI: 10.3791/407  1
2007 Chen XJ, Levedakou EN, Millen KJ, Wollmann RL, Soliven B, Popko B. Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 14515-24. PMID 18160659 DOI: 10.1523/JNEUROSCI.4338-07.2007  1
2007 Barkovich AJ, Millen KJ, Dobyns WB. A developmental classification of malformations of the brainstem. Annals of Neurology. 62: 625-39. PMID 17924529 DOI: 10.1002/ana.21239  1
2007 Chizhikov VV, Davenport J, Zhang Q, Shih EK, Cabello OA, Fuchs JL, Yoder BK, Millen KJ. Cilia proteins control cerebellar morphogenesis by promoting expansion of the granule progenitor pool. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 9780-9. PMID 17804638 DOI: 10.1523/JNEUROSCI.5586-06.2007  1
2007 Boland E, Clayton-Smith J, Woo VG, McKee S, Manson FD, Medne L, Zackai E, Swanson EA, Fitzpatrick D, Millen KJ, Sherr EH, Dobyns WB, Black GC. Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum. American Journal of Human Genetics. 81: 292-303. PMID 17668379 DOI: 10.1086/519999  1
2006 Chizhikov V, Steshina E, Roberts R, Ilkin Y, Washburn L, Millen KJ. Molecular definition of an allelic series of mutations disrupting the mouse Lmx1a (dreher) gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 1025-32. PMID 17019651 DOI: 10.1007/s00335-006-0033-7  1
2006 Pogoriler J, Millen K, Utset M, Du W. Loss of cyclin D1 impairs cerebellar development and suppresses medulloblastoma formation. Development (Cambridge, England). 133: 3929-37. PMID 16943274 DOI: 10.1242/dev.02556  1
2006 Chizhikov VV, Lindgren AG, Currle DS, Rose MF, Monuki ES, Millen KJ. The roof plate regulates cerebellar cell-type specification and proliferation. Development (Cambridge, England). 133: 2793-804. PMID 16790481 DOI: 10.1242/dev.02441  1
2006 Dumitrescu AM, Liao XH, Weiss RE, Millen K, Refetoff S. Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient mice. Endocrinology. 147: 4036-43. PMID 16709608 DOI: 10.1210/en.2006-0390  1
2005 Grinberg I, Millen KJ. The ZIC gene family in development and disease. Clinical Genetics. 67: 290-6. PMID 15733262 DOI: 10.1111/j.1399-0004.2005.00418.x  1
2005 Chizhikov VV, Millen KJ. Roof plate-dependent patterning of the vertebrate dorsal central nervous system. Developmental Biology. 277: 287-95. PMID 15617675 DOI: 10.1016/j.ydbio.2004.10.011  1
2004 Chizhikov VV, Millen KJ. Mechanisms of roof plate formation in the vertebrate CNS. Nature Reviews. Neuroscience. 5: 808-12. PMID 15378040 DOI: 10.1038/nrn1520  1
2004 Grinberg I, Northrup H, Ardinger H, Prasad C, Dobyns WB, Millen KJ. Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation. Nature Genetics. 36: 1053-5. PMID 15338008 DOI: 10.1038/ng1420  1
2004 Chizhikov VV, Millen KJ. Control of roof plate development and signaling by Lmx1b in the caudal vertebrate CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 5694-703. PMID 15215291 DOI: 10.1523/JNEUROSCI.0758-04.2004  1
2004 Millen KJ, Millonig JH, Hatten ME. Roof plate and dorsal spinal cord dl1 interneuron development in the dreher mutant mouse. Developmental Biology. 270: 382-92. PMID 15183721 DOI: 10.1016/j.ydbio.2004.03.008  1
2004 Chizhikov VV, Millen KJ. Control of roof plate formation by Lmx1a in the developing spinal cord. Development (Cambridge, England). 131: 2693-705. PMID 15148302 DOI: 10.1242/dev.01139  1
2003 Chizhikov V, Millen KJ. Development and malformations of the cerebellum in mice. Molecular Genetics and Metabolism. 80: 54-65. PMID 14567957 DOI: 10.1016/j.ymgme.2003.08.019  1
2003 Ramocki MB, Dowling J, Grinberg I, Kimonis VE, Cardoso C, Gross A, Chung J, Martin CL, Ledbetter DH, Dobyns WB, Millen KJ. Reciprocal fusion transcripts of two novel Zn-finger genes in a female with absence of the corpus callosum, ocular colobomas and a balanced translocation between chromosomes 2p24 and 9q32. European Journal of Human Genetics : Ejhg. 11: 527-34. PMID 12825074 DOI: 10.1038/sj.ejhg.5200995  1
2000 Millonig JH, Millen KJ, Hatten ME. The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS. Nature. 403: 764-9. PMID 10693804 DOI: 10.1038/35001573  1
1999 Millen KJ, Millonig JH, Wingate RJ, Alder J, Hatten ME. Neurogenetics of the cerebellar system. Journal of Child Neurology. 14: 574-81; discussion 5. PMID 10488902 DOI: 10.1177/088307389901400905  1
1996 Millonig JH, Millen KJ, Hatten ME. A high-density molecular genetic map around the weaver locus Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 926. PMID 9009075  1
1996 Vogel MW, Ji Z, Millen K, Joyner AL. The Engrailed-2 homeobox gene and patterning of spinocerebellar mossy fiber afferents. Brain Research. Developmental Brain Research. 96: 210-8. PMID 8922683 DOI: 10.1016/0165-3806(96)00122-8  1
1996 Millonig JH, Millen KJ, Hatten ME. A high-density molecular genetic map around the weaver locus. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 616-8. PMID 8678987  1
1996 Gerlai R, Millen KJ, Herrup K, Fabien K, Joyner AL, Roder J. Impaired motor learning performance in cerebellar En-2 mutant mice. Behavioral Neuroscience. 110: 126-33. PMID 8652061 DOI: 10.1037/0735-7044.110.1.126  1
1996 Kofuji P, Hofer M, Millen KJ, Millonig JH, Davidson N, Lester HA, Hatten ME. Functional analysis of the weaver mutant GIRK2 K+ channel and rescue of weaver granule cells. Neuron. 16: 941-52. PMID 8630252 DOI: 10.1016/S0896-6273(00)80117-8  1
1995 Millen KJ, Hui CC, Joyner AL. A role for En-2 and other murine homologues of Drosophila segment polarity genes in regulating positional information in the developing cerebellum. Development (Cambridge, England). 121: 3935-45. PMID 8575294  1
1994 Stroeher VL, Kennedy BP, Millen KJ, Schroeder DF, Hawkins MG, Goszczynski B, McGhee JD. DNA-protein interactions in the Caenorhabditis elegans embryo: oocyte and embryonic factors that bind to the promoter of the gut-specific ges-1 gene. Developmental Biology. 163: 367-80. PMID 8200477 DOI: 10.1006/dbio.1994.1155  1
1994 Millen KJ, Wurst W, Herrup K, Joyner AL. Abnormal embryonic cerebellar development and patterning of postnatal foliation in two mouse Engrailed-2 mutants. Development (Cambridge, England). 120: 695-706. PMID 7909289  1
1991 Davis CA, Holmyard DP, Millen KJ, Joyner AL. Examining pattern formation in mouse, chicken and frog embryos with an En-specific antiserum. Development (Cambridge, England). 111: 287-98. PMID 1680044  1
Show low-probability matches.