Year |
Citation |
Score |
2023 |
Elliott KH, Balchand SK, Bonatto Paese CL, Chang CF, Yang Y, Brown KM, Rasicci DT, He H, Thorner K, Chaturvedi P, Murray SA, Chen J, Porollo A, Peterson KA, Brugmann SA. Identification of a heterogeneous and dynamic ciliome during embryonic development and cell differentiation. Development (Cambridge, England). PMID 36971348 DOI: 10.1242/dev.201237 |
0.349 |
|
2021 |
Pagliaroli L, Porazzi P, Curtis AT, Scopa C, Mikkers HMM, Freund C, Daxinger L, Deliard S, Welsh SA, Offley S, Ott CA, Calabretta B, Brugmann SA, Santen GWE, Trizzino M. Inability to switch from ARID1A-BAF to ARID1B-BAF impairs exit from pluripotency and commitment towards neural crest formation in ARID1B-related neurodevelopmental disorders. Nature Communications. 12: 6469. PMID 34753942 DOI: 10.1038/s41467-021-26810-x |
0.327 |
|
2021 |
Brooks EC, Bonatto Paese CL, Carroll AH, Struve JN, Nagy N, Brugmann SA. Mutation in the Ciliary Protein C2CD3 Reveals Organ-Specific Mechanisms of Hedgehog Signal Transduction in Avian Embryos. Journal of Developmental Biology. 9. PMID 33805906 DOI: 10.3390/jdb9020012 |
0.347 |
|
2021 |
Brugmann S, Clouthier DE, Saint-Jeannet JP, Taneyhill LA, Moody SA. The society for craniofacial genetics and developmental biology 43rd annual meeting. American Journal of Medical Genetics. Part A. PMID 33660912 DOI: 10.1002/ajmg.a.62150 |
0.535 |
|
2021 |
Bonatto Paese CL, Brooks EC, Aarnio-Peterson M, Brugmann SA. Ciliopathic micrognathia is caused by aberrant skeletal differentiation and remodeling. Development (Cambridge, England). 148. PMID 33589509 DOI: 10.1242/dev.194175 |
0.351 |
|
2020 |
Elliott KH, Chen X, Salomone J, Chaturvedi P, Schultz PA, Balchand SK, Servetas JD, Zuniga A, Zeller R, Gebelein B, Weirauch MT, Peterson KA, Brugmann SA. Gli3 utilizes Hand2 to synergistically regulate tissue-specific transcriptional networks. Elife. 9. PMID 33006313 DOI: 10.7554/eLife.56450 |
0.344 |
|
2020 |
Lavery WJ, Kotliar M, Chang CF, Brugmann SA, Barski A, Lindsley AW. KMT2D
Haploinsufficiency in Kabuki Syndrome Impairs Differentiation of Neural Crest Cells The Faseb Journal. 34: 1-1. DOI: 10.1096/Fasebj.2020.34.S1.09189 |
0.367 |
|
2018 |
Metzler MA, Raja S, Elliott KH, Friedl RM, Tran NQH, Brugmann SA, Larsen M, Sandell LL. RDH10-mediated retinol metabolism and RARα-mediated retinoic acid signaling are required for submandibular salivary gland initiation. Development (Cambridge, England). PMID 29986869 DOI: 10.1242/Dev.164822 |
0.368 |
|
2018 |
Elliott KH, Brugmann SA. Sending mixed signals: Cilia-dependent signaling during development and disease. Developmental Biology. PMID 29548942 DOI: 10.1016/J.Ydbio.2018.03.007 |
0.389 |
|
2018 |
Elliott KH, Millington G, Brugmann SA. A novel role for cilia-dependent Sonic hedgehog signaling during submandibular gland development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. PMID 29532549 DOI: 10.1002/Dvdy.24627 |
0.394 |
|
2017 |
Schock EN, Brugmann SA. Neural crest cells utilize primary cilia to regulate ventral forebrain morphogenesis via Hedgehog-dependent regulation of oriented cell division. Developmental Biology. PMID 28941984 DOI: 10.1016/J.Ydbio.2017.09.026 |
0.481 |
|
2017 |
Schock EN, Struve JN, Chang CF, Williams TJ, Snedeker J, Attia AC, Stottmann RW, Brugmann SA. A tissue-specific role for intraflagellar transport genes during craniofacial development. Plos One. 12: e0174206. PMID 28346501 DOI: 10.1371/Journal.Pone.0174206 |
0.441 |
|
2017 |
Snedeker J, Schock EN, Struve JN, Chang CF, Cionni M, Tran PV, Brugmann SA, Stottmann RW. Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development. Plos One. 12: e0173258. PMID 28291836 DOI: 10.1371/Journal.Pone.0173258 |
0.441 |
|
2017 |
Millington G, Elliott K, Chang YT, Chang CF, Dlugosz A, Brugmann SA. Cilia-dependent GLI processing in neural crest cells is required for tongue development. Developmental Biology. PMID 28286175 DOI: 10.1016/J.Ydbio.2017.02.021 |
0.4 |
|
2017 |
Schock EN, Brugmann SA. Discovery, Diagnosis, and Etiology of Craniofacial Ciliopathies. Cold Spring Harbor Perspectives in Biology. PMID 28213462 DOI: 10.1101/Cshperspect.A028258 |
0.383 |
|
2016 |
Workman MJ, Mahe MM, Trisno S, Poling HM, Watson CL, Sundaram N, Chang CF, Schiesser J, Aubert P, Stanley EG, Elefanty AG, Miyaoka Y, Mandegar MA, Conklin BR, Neunlist M, ... Brugmann SA, et al. Engineered human pluripotent-stem-cell-derived intestinal tissues with a functional enteric nervous system. Nature Medicine. PMID 27869805 DOI: 10.1038/Nm.4233 |
0.354 |
|
2016 |
Chang CF, Chang YT, Millington G, Brugmann SA. Craniofacial Ciliopathies Reveal Specific Requirements for GLI Proteins during Development of the Facial Midline. Plos Genetics. 12: e1006351. PMID 27802276 DOI: 10.1371/Journal.Pgen.1006351 |
0.427 |
|
2016 |
Chang YT, Chaturvedi P, Schock EN, Brugmann SA. Understanding Mechanisms of GLI-Mediated Transcription during Craniofacial Development and Disease Using the Ciliopathic Mutant, talpid(2). Frontiers in Physiology. 7: 468. PMID 27799912 DOI: 10.3389/Fphys.2016.00468 |
0.435 |
|
2015 |
Romick-Rosendale LE, Hoskins EE, Privette Vinnedge LM, Foglesong GD, Brusadelli MG, Potter SS, Komurov K, Brugmann SA, Lambert P, Kimple RJ, Virts EL, Hanenberg H, Gillison ML, Wells SI. Defects in the Fanconi anemia pathway in head and neck cancer cells stimulate tumor cell invasion through DNA-PK and Rac1 signaling. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 26603260 DOI: 10.1158/1078-0432.Ccr-15-2209 |
0.347 |
|
2015 |
Schock EN, Chang CF, Youngworth IA, Davey MG, Delany ME, Brugmann SA. Utilizing the chicken as an animal model for human craniofacial ciliopathies. Developmental Biology. PMID 26597494 DOI: 10.1016/J.Ydbio.2015.10.024 |
0.348 |
|
2015 |
Schock EN, Chang CF, Struve JN, Chang YT, Chang J, Delany ME, Brugmann SA. Using the avian mutant talpid2 as a disease model for understanding the oral-facial phenotypes of oral-facial-digital syndrome. Disease Models & Mechanisms. 8: 855-66. PMID 26044959 DOI: 10.1242/Dmm.020222 |
0.403 |
|
2015 |
Saal HM, Prows CA, Guerreiro I, Donlin M, Knudson L, Sund KL, Chang CF, Brugmann SA, Stottmann RW. A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia. Human Molecular Genetics. 24: 3399-409. PMID 25759469 DOI: 10.1093/Hmg/Ddv088 |
0.325 |
|
2015 |
Chang CF, Schock EN, Attia AC, Stottmann RW, Brugmann SA. The ciliary baton: orchestrating neural crest cell development. Current Topics in Developmental Biology. 111: 97-134. PMID 25662259 DOI: 10.1016/Bs.Ctdb.2014.11.004 |
0.45 |
|
2015 |
Schock E, Chang C, Struve J, Chang J, Brugmann S. Using the talpid2 as novel model for determining the cellular and molecular etiology of Oral-facial-digital syndrome. Cilia. 4: 41. DOI: 10.1186/2046-2530-4-S1-P41 |
0.357 |
|
2014 |
Chang CF, Schock EN, O'Hare EA, Dodgson J, Cheng HH, Muir WM, Edelmann RE, Delany ME, Brugmann SA. The cellular and molecular etiology of the craniofacial defects in the avian ciliopathic mutant talpid2. Development (Cambridge, England). 141: 3003-12. PMID 25053433 DOI: 10.1242/Dev.105924 |
0.42 |
|
2013 |
Brugmann SA, Wells JM. Building additional complexity to in vitro-derived intestinal tissues. Stem Cell Research & Therapy. 4: S1. PMID 24565179 DOI: 10.1186/Scrt362 |
0.319 |
|
2013 |
Liu H, Lan Y, Xu J, Chang CF, Brugmann SA, Jiang R. Odd-skipped related-1 controls neural crest chondrogenesis during tongue development. Proceedings of the National Academy of Sciences of the United States of America. 110: 18555-60. PMID 24167250 DOI: 10.1073/Pnas.1306495110 |
0.492 |
|
2012 |
Rada-Iglesias A, Bajpai R, Prescott S, Brugmann SA, Swigut T, Wysocka J. Epigenomic annotation of enhancers predicts transcriptional regulators of human neural crest. Cell Stem Cell. 11: 633-48. PMID 22981823 DOI: 10.1016/J.Stem.2012.07.006 |
0.404 |
|
2012 |
Powder KE, Ku YC, Brugmann SA, Veile RA, Renaud NA, Helms JA, Lovett M. A cross-species analysis of microRNAs in the developing avian face. Plos One. 7: e35111. PMID 22523571 DOI: 10.1371/Journal.Pone.0035111 |
0.316 |
|
2011 |
Lenton K, James AW, Manu A, Brugmann SA, Birker D, Nelson ER, Leucht P, Helms JA, Longaker MT. Indian hedgehog positively regulates calvarial ossification and modulates bone morphogenetic protein signaling. Genesis (New York, N.Y. : 2000). 49: 784-96. PMID 21557453 DOI: 10.1002/Dvg.20768 |
0.358 |
|
2011 |
Levi B, James AW, Nelson ER, Brugmann SA, Sorkin M, Manu A, Longaker MT. Role of Indian hedgehog signaling in palatal osteogenesis. Plastic and Reconstructive Surgery. 127: 1182-90. PMID 21364421 DOI: 10.1097/Prs.0B013E3182043A07 |
0.388 |
|
2011 |
Zaghloul NA, Brugmann SA. The emerging face of primary cilia. Genesis (New York, N.Y. : 2000). 49: 231-46. PMID 21305689 DOI: 10.1002/Dvg.20728 |
0.644 |
|
2011 |
Cordero DR, Brugmann S, Chu Y, Bajpai R, Jame M, Helms JA. Cranial neural crest cells on the move: their roles in craniofacial development. American Journal of Medical Genetics. Part A. 155: 270-9. PMID 21271641 DOI: 10.1002/Ajmg.A.33702 |
0.434 |
|
2011 |
Rada-Iglesias A, Bajpai R, Swigut T, Brugmann SA, Flynn RA, Wysocka J. A unique chromatin signature uncovers early developmental enhancers in humans. Nature. 470: 279-83. PMID 21160473 DOI: 10.1038/Nature09692 |
0.371 |
|
2011 |
Levi B, Brugmann S, Longaker MT. Discussion: Hes1 is required for the development of craniofacial structures derived from ectomesenchymal neural crest cells. The Journal of Craniofacial Surgery. 21: 1450-1. PMID 20818250 DOI: 10.1097/Scs.0B013E3181Ecc54B |
0.379 |
|
2011 |
Nelson E, Levi B, Sorkin M, James A, Brugmann S, Longaker M. 104: ROLE OF GSK-3B SIGNALING IN PALATAL OSTEOGENESIS: IN VITRO AND IN VIVO STUDIES Plastic and Reconstructive Surgery. 127: 60. DOI: 10.1097/01.Prs.0000396791.75313.58 |
0.301 |
|
2010 |
Brugmann SA, Cordero DR, Helms JA. Craniofacial ciliopathies: A new classification for craniofacial disorders. American Journal of Medical Genetics. Part A. 152: 2995-3006. PMID 21108387 DOI: 10.1002/Ajmg.A.33727 |
0.343 |
|
2010 |
Brugmann SA, Allen NC, James AW, Mekonnen Z, Madan E, Helms JA. A primary cilia-dependent etiology for midline facial disorders. Human Molecular Genetics. 19: 1577-92. PMID 20106874 DOI: 10.1093/Hmg/Ddq030 |
0.459 |
|
2010 |
Brugmann SA, Powder KE, Young NM, Goodnough LH, Hahn SM, James AW, Helms JA, Lovett M. Comparative gene expression analysis of avian embryonic facial structures reveals new candidates for human craniofacial disorders. Human Molecular Genetics. 19: 920-30. PMID 20015954 DOI: 10.1093/Hmg/Ddp559 |
0.47 |
|
2010 |
Brugmann S, Allen NC, James AW, Mekonnen Z, Madan E, Helms JA. Loss of primary cilia affect neural crest cell behavior and leads to craniofacial defects Developmental Biology. 344: 467. DOI: 10.1016/J.Ydbio.2010.05.216 |
0.359 |
|
2008 |
ten Berge D, Brugmann SA, Helms JA, Nusse R. Wnt and FGF signals interact to coordinate growth with cell fate specification during limb development. Development (Cambridge, England). 135: 3247-57. PMID 18776145 DOI: 10.1242/Dev.023176 |
0.426 |
|
2008 |
Anderson CT, Castillo AB, Brugmann SA, Helms JA, Jacobs CR, Stearns T. Primary cilia: cellular sensors for the skeleton. Anatomical Record (Hoboken, N.J. : 2007). 291: 1074-8. PMID 18727074 DOI: 10.1002/Ar.20754 |
0.386 |
|
2008 |
Schlosser G, Awtry T, Brugmann SA, Jensen ED, Neilson K, Ruan G, Stammler A, Voelker D, Yan B, Zhang C, Klymkowsky MW, Moody SA. Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion. Developmental Biology. 320: 199-214. PMID 18571637 DOI: 10.1016/J.Ydbio.2008.05.523 |
0.579 |
|
2007 |
Brugmann SA, Goodnough LH, Gregorieff A, Leucht P, ten Berge D, Fuerer C, Clevers H, Nusse R, Helms JA. Wnt signaling mediates regional specification in the vertebrate face. Development (Cambridge, England). 134: 3283-95. PMID 17699607 DOI: 10.1242/Dev.005132 |
0.413 |
|
2007 |
Rinn JL, Kertesz M, Wang JK, Squazzo SL, Xu X, Brugmann SA, Goodnough LH, Helms JA, Farnham PJ, Segal E, Chang HY. Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs. Cell. 129: 1311-23. PMID 17604720 DOI: 10.1016/J.Cell.2007.05.022 |
0.349 |
|
2007 |
Goodnough LH, Brugmann SA, Hu D, Helms JA. Stage-dependent craniofacial defects resulting from Sprouty2 overexpression. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 236: 1918-28. PMID 17576140 DOI: 10.1002/Dvdy.21195 |
0.45 |
|
2007 |
Helms JA, Brugmann SA. The origins of species-specific facial morphology: The proof is in the pigeon Integrative and Comparative Biology. 47: 338-342. DOI: 10.1093/Icb/Icm051 |
0.327 |
|
2006 |
Brugmann SA, Kim J, Helms JA. Looking different: Understanding diversity in facial form American Journal of Medical Genetics, Part A. 140: 2521-2529. PMID 16838331 DOI: 10.1002/Ajmg.A.31361 |
0.389 |
|
2006 |
Brugmann SA, Tapadia MD, Helms JA. The molecular origins of species-specific facial pattern. Current Topics in Developmental Biology. 73: 1-42. PMID 16782454 DOI: 10.1016/S0070-2153(05)73001-5 |
0.408 |
|
2005 |
Brugmann SA, Moody SA. Induction and specification of the vertebrate ectodermal placodes: precursors of the cranial sensory organs. Biology of the Cell / Under the Auspices of the European Cell Biology Organization. 97: 303-19. PMID 15836430 DOI: 10.1042/Bc20040515 |
0.634 |
|
2004 |
Brugmann SA, Pandur PD, Kenyon KL, Pignoni F, Moody SA. Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor. Development (Cambridge, England). 131: 5871-81. PMID 15525662 DOI: 10.1242/Dev.01516 |
0.67 |
|
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