| Year |
Citation |
Score |
| 2024 |
Saulnier O, Zagozewski J, Liang L, Hendrikse LD, Layug P, Gordon V, Aldinger KA, Haldipur P, Borlase S, Coudière-Morrison L, Cai T, Martell E, Gonzales NM, Palidwor G, Porter CJ, ... ... Millen KJ, et al. A group 3 medulloblastoma stem cell program is maintained by OTX2-mediated alternative splicing. Nature Cell Biology. PMID 39025928 DOI: 10.1038/s41556-024-01460-5 |
0.79 |
|
| 2024 |
Visvanathan A, Saulnier O, Chen C, Haldipur P, Orisme W, Delaidelli A, Shin S, Millman J, Bryant A, Abeysundara N, Wu X, Hendrikse LD, Patil V, Bashardanesh Z, Golser J, ... ... Millen KJ, et al. Early rhombic lip Protogenin stem cells in a human-specific neurovascular niche initiate and maintain group 3 medulloblastoma. Cell. PMID 38971152 DOI: 10.1016/j.cell.2024.06.011 |
0.792 |
|
| 2024 |
Stock AJ, Gonzalez Paredes P, de Almeida LP, Kosanke SD, Chetlur S, Budde H, Wakenight P, Zwingman TA, Rosen ABI, Allenspach EJ, Millen KJ, Buckner JH, Rawlings DJ, Gorman JA. The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner. Frontiers in Immunology. 15: 1349601. PMID 38487540 DOI: 10.3389/fimmu.2024.1349601 |
0.775 |
|
| 2024 |
Stock AJ, Gonzalez-Paredes P, Previato de Almeida L, Kosanke SD, Chetlur S, Budde H, Wakenight P, Zwingman TA, Rosen AB, Allenspach E, Millen KJ, Buckner JH, Rawlings DJ, Gorman JA. The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner. Biorxiv : the Preprint Server For Biology. PMID 38328221 DOI: 10.1101/2024.01.20.576482 |
0.775 |
|
| 2023 |
Nguyen ED, Fard VN, Kim BY, Collins S, Galey M, Nelson BR, Wakenight P, Gable SM, McKenna A, Bammler TK, MacDonald J, Okamura DM, Shendure J, Beier DR, Ramirez JM, ... ... Millen KJ, et al. GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus). G3 (Bethesda, Md.). PMID 37552705 DOI: 10.1093/g3journal/jkad177 |
0.766 |
|
| 2023 |
Butler DF, Skibo J, Traudt CM, Millen KJ. Neonatal subarachnoid hemorrhage disrupts multiple aspects of cerebellar development. Frontiers in Molecular Neuroscience. 16: 1161086. PMID 37187957 DOI: 10.3389/fnmol.2023.1161086 |
0.784 |
|
| 2023 |
Nguyen ED, Fard VN, Kim BY, Collins S, Galey M, Nelson BR, Wakenight P, Gable SM, McKenna A, Bammler TK, MacDonald J, Okamura DM, Shendure J, Beier DR, Ramirez JM, ... ... Millen KJ, et al. GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse ( ). Biorxiv : the Preprint Server For Biology. PMID 37066261 DOI: 10.1101/2023.04.03.535372 |
0.766 |
|
| 2023 |
Butler DF, Skibo J, Traudt CM, Millen KJ. Neonatal Subarachnoid Hemorrhage Disrupts Multiple Aspects of Cerebellar Development. Biorxiv : the Preprint Server For Biology. PMID 36798230 DOI: 10.1101/2023.02.10.528048 |
0.784 |
|
| 2022 |
Hendrikse LD, Haldipur P, Saulnier O, Millman J, Sjoboen AH, Erickson AW, Ong W, Gordon V, Coudière-Morrison L, Mercier AL, Shokouhian M, Suárez RA, Ly M, Borlase S, Scott DS, ... ... Millen KJ, et al. Author Correction: Failure of human rhombic lip differentiation underlies medulloblastoma formation. Nature. PMID 36446943 DOI: 10.1038/s41586-022-05578-0 |
0.774 |
|
| 2022 |
Smith KS, Bihannic L, Gudenas BL, Haldipur P, Tao R, Gao Q, Li Y, Aldinger KA, Iskusnykh IY, Chizhikov VV, Scoggins M, Zhang S, Edwards A, Deng M, Glass IA, ... ... Millen KJ, et al. Unified rhombic lip origins of group 3 and group 4 medulloblastoma. Nature. 609: 1012-1020. PMID 36131015 DOI: 10.1038/s41586-022-05208-9 |
0.795 |
|
| 2022 |
Hendrikse LD, Haldipur P, Saulnier O, Millman J, Sjoboen AH, Erickson AW, Ong W, Gordon V, Coudière-Morrison L, Mercier AL, Shokouhian M, Suárez RA, Ly M, Borlase S, Scott DS, ... ... Millen KJ, et al. Failure of human rhombic lip differentiation underlies medulloblastoma formation. Nature. PMID 36131014 DOI: 10.1038/s41586-022-05215-w |
0.812 |
|
| 2022 |
Wei AD, Wakenight P, Zwingman TA, Bard AM, Sahai N, Willemsen MH, Schelhaas HJ, Stegmann APA, Verhoeven JS, de Man SA, Wessels MW, Kleefstra T, Shinde DN, Helbig KL, Basinger A, ... ... Millen KJ, et al. Human KCNQ5 de novo Mutations Underlie Epilepsy and Intellectual Disability. Journal of Neurophysiology. PMID 35583973 DOI: 10.1152/jn.00509.2021 |
0.78 |
|
| 2022 |
Haldipur P, Millen KJ, Aldinger KA. Human Cerebellar Development and Transcriptomics: Implications for Neurodevelopmental Disorders. Annual Review of Neuroscience. PMID 35440142 DOI: 10.1146/annurev-neuro-111020-091953 |
0.807 |
|
| 2021 |
Roy A, Han VZ, Bard AM, Wehle DT, Smith SEP, Ramirez JM, Kalume F, Millen KJ. Non-synaptic Cell-Autonomous Mechanisms Underlie Neuronal Hyperactivity in a Genetic Model of -Driven Intractable Epilepsy. Frontiers in Molecular Neuroscience. 14: 772847. PMID 34899181 DOI: 10.3389/fnmol.2021.772847 |
0.591 |
|
| 2021 |
Okamura DM, Brewer CM, Wakenight P, Bahrami N, Bernardi K, Tran A, Olson J, Shi X, Yeh SY, Piliponsky A, Collins SJ, Nguyen ED, Timms AE, MacDonald JW, Bammler TK, ... ... Millen KJ, et al. Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis. Iscience. 24: 103269. PMID 34849462 DOI: 10.1016/j.isci.2021.103269 |
0.779 |
|
| 2021 |
Brewer CM, Nelson BR, Wakenight P, Collins SJ, Okamura DM, Dong XR, Mahoney WM, McKenna A, Shendure J, Timms A, Millen KJ, Majesky MW. Adaptations in Hippo-Yap signaling and myofibroblast fate underlie scar-free ear appendage wound healing in spiny mice. Developmental Cell. PMID 34610329 DOI: 10.1016/j.devcel.2021.09.008 |
0.785 |
|
| 2021 |
Haldipur P, Bernardo S, Aldinger KA, Sivakumar T, Millman J, Sjoboen AH, Dang D, Dubocanin D, Deng M, Timms AE, Davis BD, Plummer JT, Mankad K, Oztekin O, Manganaro L, ... ... Millen KJ, et al. Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformation. Acta Neuropathologica. PMID 34347142 DOI: 10.1007/s00401-021-02355-7 |
0.807 |
|
| 2021 |
Aldinger KA, Thomson Z, Phelps IG, Haldipur P, Deng M, Timms AE, Hirano M, Santpere G, Roco C, Rosenberg AB, Lorente-Galdos B, Gulden FO, O'Day D, Overman LM, Lisgo SN, ... ... Millen KJ, et al. Spatial and cell type transcriptional landscape of human cerebellar development. Nature Neuroscience. PMID 34140698 DOI: 10.1038/s41593-021-00872-y |
0.806 |
|
| 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 |
0.583 |
|
| 2020 |
Nelson BR, Hodge RD, Daza RA, Tripathi PP, Arnold SJ, Millen KJ, Hevner RF. Intermediate progenitors support migration of neural stem cells into dentate gyrus outer neurogenic niches. Elife. 9. PMID 32238264 DOI: 10.7554/Elife.53777 |
0.608 |
|
| 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 |
0.799 |
|
| 2020 |
Butler D, Traudt C, Skibo J, Zwingman T, Millen K. 693 Critical Care Medicine. 48: 327. DOI: 10.1097/01.Ccm.0000626512.29198.Bc |
0.736 |
|
| 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 |
0.798 |
|
| 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 |
0.807 |
|
| 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 |
0.793 |
|
| 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 |
0.808 |
|
| 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 |
0.738 |
|
| 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 |
0.762 |
|
| 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 |
0.741 |
|
| 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 |
0.824 |
|
| 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 |
0.79 |
|
| 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 |
0.787 |
|
| 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 |
0.785 |
|
| 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 |
0.575 |
|
| 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 |
0.755 |
|
| 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 |
0.797 |
|
| 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 |
0.664 |
|
| 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 |
0.558 |
|
| 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 |
0.804 |
|
| 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 |
0.733 |
|
| 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 |
0.475 |
|
| 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 |
0.616 |
|
| 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 |
0.463 |
|
| 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 |
0.635 |
|
| 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 |
0.684 |
|
| 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 |
0.81 |
|
| 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 |
0.438 |
|
| 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 |
0.757 |
|
| 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 |
0.327 |
|
| 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 |
0.445 |
|
| 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 |
0.773 |
|
| 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 |
0.498 |
|
| 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 |
0.697 |
|
| 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 |
0.5 |
|
| 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 |
0.581 |
|
| 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 |
0.718 |
|
| 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 |
0.777 |
|
| 2011 |
Doherty D, Millen KJ. Wormless without wingless. Nature Medicine. 17: 663-5. PMID 21647144 DOI: 10.1038/Nm0611-663 |
0.497 |
|
| 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 |
0.779 |
|
| 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 |
0.787 |
|
| 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 |
0.783 |
|
| 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 |
0.807 |
|
| 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 |
0.408 |
|
| 2010 |
Aldinger K, Blank M, Lehmann O, Dobyns W, Millen K. [S7.3]: Cerebellar malformations in mice and humans illuminate novel developmental principles International Journal of Developmental Neuroscience. 28: 651-651. DOI: 10.1016/J.Ijdevneu.2010.07.036 |
0.789 |
|
| 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 |
0.489 |
|
| 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 |
0.571 |
|
| 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 |
0.753 |
|
| 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 |
0.722 |
|
| 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 |
0.819 |
|
| 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 |
0.766 |
|
| 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 |
0.597 |
|
| 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 |
0.756 |
|
| 2008 |
Blank MC, Grinberg I, Chizhikov VV, Millen KJ. Zic1 and Zic4 are required for mammalian cerebellar patterning and growth Developmental Biology. 319: 594-595. DOI: 10.1016/J.Ydbio.2008.05.506 |
0.71 |
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| 2008 |
Mishima Y, Lindgren A, Chizhikov V, Johnson R, Millen K. Lmx1a and Lmx1b have redundant function in the development of the hindbrain roof plate and the cerebellum International Journal of Developmental Neuroscience. 26: 856. DOI: 10.1016/J.Ijdevneu.2008.09.095 |
0.635 |
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| 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 |
0.645 |
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| 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 |
0.44 |
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| 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 |
0.82 |
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| 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 |
0.449 |
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| 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 |
0.619 |
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| 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 |
0.77 |
|
| 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 |
0.573 |
|
| 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 |
0.519 |
|
| 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 |
0.532 |
|
| 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 |
0.674 |
|
| 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 |
0.521 |
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| 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 |
0.59 |
|
| 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 |
0.537 |
|
| 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 |
0.617 |
|
| 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 |
0.625 |
|
| 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 |
0.589 |
|
| 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 |
0.619 |
|
| 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 |
0.511 |
|
| 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 |
0.49 |
|
| 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 DOI: 10.1007/S003359900183 |
0.511 |
|
| 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 |
0.498 |
|
| 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 |
0.57 |
|
| 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 |
0.507 |
|
| 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 |
0.46 |
|
| 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 |
0.552 |
|
| 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 |
0.506 |
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