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Items: 1 to 50 of 111


Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice.

Motch Perrine SM, Wu M, Stephens NB, Kriti D, van Bakel H, Jabs EW, Richtsmeier JT.

Dis Model Mech. 2019 May 30;12(5). pii: dmm038513. doi: 10.1242/dmm.038513.


A coupled reaction-diffusion-strain model predicts cranial vault formation in development and disease.

Lee C, Richtsmeier JT, Kraft RH.

Biomech Model Mechanobiol. 2019 Aug;18(4):1197-1211. doi: 10.1007/s10237-019-01139-z. Epub 2019 Apr 20.


Craniofacial skeletal response to encephalization: How do we know what we think we know?

Lesciotto KM, Richtsmeier JT.

Am J Phys Anthropol. 2019 Jan;168 Suppl 67:27-46. doi: 10.1002/ajpa.23766.


Nonsyndromic craniosynostosis: novel coding variants.

Sewda A, White SR, Erazo M, Hao K, García-Fructuoso G, Fernández-Rodriguez I, Heuzé Y, Richtsmeier JT, Romitti PA, Reva B, Jabs EW, Peter I.

Pediatr Res. 2019 Mar;85(4):463-468. doi: 10.1038/s41390-019-0274-2. Epub 2019 Jan 14.


It's about Time: Ossification Center Formation in C57BL/6 Mice from E12⁻E16.

Flaherty K, Richtsmeier JT.

J Dev Biol. 2018 Dec 15;6(4). pii: E31. doi: 10.3390/jdb6040031.


Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects.

Holmes G, O'Rourke C, Motch Perrine SM, Lu N, van Bakel H, Richtsmeier JT, Jabs EW.

Development. 2018 Oct 5;145(19). pii: dev166488. doi: 10.1242/dev.166488.


A century of development.

Richtsmeier JT.

Am J Phys Anthropol. 2018 Apr;165(4):726-740. doi: 10.1002/ajpa.23379. No abstract available.


A quantitative method for staging mouse embryos based on limb morphometry.

Musy M, Flaherty K, Raspopovic J, Robert-Moreno A, Richtsmeier JT, Sharpe J.

Development. 2018 Apr 5;145(7). pii: dev154856. doi: 10.1242/dev.154856.


Choanal Atresia and Craniosynostosis: Development and Disease.

Lesciotto KM, Heuzé Y, Jabs EW, Bernstein JM, Richtsmeier JT.

Plast Reconstr Surg. 2018 Jan;141(1):156-168. doi: 10.1097/PRS.0000000000003928. Review.



Lee C, Richtsmeier JT, Kraft RH.

J Mech Med Biol. 2017 Jun;17(4). pii: 1750073. doi: 10.1142/S0219519417500737. Epub 2017 May 29.


Additive genetic variation in the craniofacial skeleton of baboons (genus Papio) and its relationship to body and cranial size.

Joganic JL, Willmore KE, Richtsmeier JT, Weiss KM, Mahaney MC, Rogers J, Cheverud JM.

Am J Phys Anthropol. 2018 Feb;165(2):269-285. doi: 10.1002/ajpa.23349. Epub 2017 Nov 20.


The Influence of trisomy 21 on facial form and variability.

Starbuck JM, Cole TM 3rd, Reeves RH, Richtsmeier JT.

Am J Med Genet A. 2017 Nov;173(11):2861-2872. doi: 10.1002/ajmg.a.38464. Epub 2017 Sep 21.


Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes.

Motch Perrine SM, Stecko T, Neuberger T, Jabs EW, Ryan TM, Richtsmeier JT.

Front Hum Neurosci. 2017 Jul 25;11:369. doi: 10.3389/fnhum.2017.00369. eCollection 2017.


The society for craniofacial genetics and developmental biology 39th annual meeting.

Fish JL, Albertson C, Harris MP, Lozanoff S, Marcucio RS, Richtsmeier JT, Trainor PA.

Am J Med Genet A. 2017 Apr;173(4):985-1006. doi: 10.1002/ajmg.a.38096. Epub 2017 Feb 7.


Developmental and Evolutionary Significance of the Zygomatic Bone.

Heuzé Y, Kawasaki K, Schwarz T, Schoenebeck JJ, Richtsmeier JT.

Anat Rec (Hoboken). 2016 Dec;299(12):1616-1630. doi: 10.1002/ar.23449.


A Critical Evaluation of the Down Syndrome Diagnosis for LB1, Type Specimen of Homo floresiensis.

Baab KL, Brown P, Falk D, Richtsmeier JT, Hildebolt CF, Smith K, Jungers W.

PLoS One. 2016 Jun 8;11(6):e0155731. doi: 10.1371/journal.pone.0155731. eCollection 2016.


The society for craniofacial genetics and developmental biology 38th annual meeting.

Taneyhill LA, Hoover-Fong J, Lozanoff S, Marcucio R, Richtsmeier JT, Trainor PA.

Am J Med Genet A. 2016 Jul;170(7):1732-53. doi: 10.1002/ajmg.a.37651. Epub 2016 Apr 22.


Understanding craniosynostosis as a growth disorder.

Flaherty K, Singh N, Richtsmeier JT.

Wiley Interdiscip Rev Dev Biol. 2016 Jul;5(4):429-59. doi: 10.1002/wdev.227. Epub 2016 Mar 22. Review.


Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.

Ye X, Guilmatre A, Reva B, Peter I, Heuzé Y, Richtsmeier JT, Fox DJ, Goedken RJ, Jabs EW, Romitti PA.

Plast Reconstr Surg. 2016 Mar;137(3):952-61. doi: 10.1097/


Chronic up-regulation of sonic hedgehog has little effect on postnatal craniofacial morphology of euploid and trisomic mice.

Singh N, Dutka T, Reeves RH, Richtsmeier JT.

Dev Dyn. 2016 Feb;245(2):114-22. doi: 10.1002/dvdy.24361. Epub 2015 Dec 6.


Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.

Heuzé Y, Holmes G, Peter I, Richtsmeier JT, Jabs EW.

Curr Genet Med Rep. 2014 Sep 1;2(3):135-145.



Lee C, Richtsmeier JT, Kraft RH.

Int Mech Eng Congress Expo. 2014 Nov;2014. pii: V009T12A061.


A computational analysis of bone formation in the cranial vault in the mouse.

Lee C, Richtsmeier JT, Kraft RH.

Front Bioeng Biotechnol. 2015 Mar 19;3:24. doi: 10.3389/fbioe.2015.00024. eCollection 2015.


Facing up to the challenges of advancing Craniofacial Research.

Trainor PA, Richtsmeier JT.

Am J Med Genet A. 2015 Jul;167(7):1451-4. doi: 10.1002/ajmg.a.37065. Epub 2015 Mar 28.


The Society for Craniofacial Genetics and Developmental Biology 37th annual meeting.

Richtsmeier JT, Jones MC, Lozanoff S, Trainor PA.

Am J Med Genet A. 2015 Jul;167(7):1455-73. doi: 10.1002/ajmg.a.37012. Epub 2015 Mar 30. No abstract available.


Acute upregulation of hedgehog signaling in mice causes differential effects on cranial morphology.

Singh N, Dutka T, Devenney BM, Kawasaki K, Reeves RH, Richtsmeier JT.

Dis Model Mech. 2015 Mar;8(3):271-9. doi: 10.1242/dmm.017889. Epub 2014 Dec 24.


Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice.

Starbuck JM, Dutka T, Ratliff TS, Reeves RH, Richtsmeier JT.

Am J Med Genet A. 2014 Aug;164A(8):1981-1990. doi: 10.1002/ajmg.a.36594. Epub 2014 May 1.


Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues.

Heuzé Y, Singh N, Basilico C, Jabs EW, Holmes G, Richtsmeier JT.

Bone. 2014 Jun;63:101-9. doi: 10.1016/j.bone.2014.03.003. Epub 2014 Mar 13.


Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice.

Motch Perrine SM, Cole TM 3rd, Martínez-Abadías N, Aldridge K, Jabs EW, Richtsmeier JT.

BMC Dev Biol. 2014 Feb 28;14:8. doi: 10.1186/1471-213X-14-8.


Quantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.

Heuzé Y, Martínez-Abadías N, Stella JM, Arnaud E, Collet C, García Fructuoso G, Alamar M, Lo LJ, Boyadjiev SA, Di Rocco F, Richtsmeier JT.

Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):250-9. doi: 10.1002/bdra.23228. Epub 2014 Feb 27.


Embryonic craniofacial bone volume and bone mineral density in Fgfr2(+/P253R) and nonmutant mice.

Percival CJ, Huang Y, Jabs EW, Li R, Richtsmeier JT.

Dev Dyn. 2014 Apr;243(4):541-51. doi: 10.1002/dvdy.24095. Epub 2014 Feb 7.


Angiogenesis and intramembranous osteogenesis.

Percival CJ, Richtsmeier JT.

Dev Dyn. 2013 Aug;242(8):909-22. doi: 10.1002/dvdy.23992. Epub 2013 Jun 27. Review.


Hand in glove: brain and skull in development and dysmorphogenesis.

Richtsmeier JT, Flaherty K.

Acta Neuropathol. 2013 Apr;125(4):469-89. doi: 10.1007/s00401-013-1104-y. Epub 2013 Mar 23. Review.


From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome.

Martínez-Abadías N, Holmes G, Pankratz T, Wang Y, Zhou X, Jabs EW, Richtsmeier JT.

Dis Model Mech. 2013 May;6(3):768-79. doi: 10.1242/dmm.010397. Epub 2013 Mar 8.


Trisomy 21 and facial developmental instability.

Starbuck JM, Cole TM 3rd, Reeves RH, Richtsmeier JT.

Am J Phys Anthropol. 2013 May;151(1):49-57. doi: 10.1002/ajpa.22255. Epub 2013 Mar 15.


Postnatal brain and skull growth in an Apert syndrome mouse model.

Hill CA, Martínez-Abadías N, Motch SM, Austin JR, Wang Y, Jabs EW, Richtsmeier JT, Aldridge K.

Am J Med Genet A. 2013 Apr;161A(4):745-57. doi: 10.1002/ajmg.a.35805. Epub 2013 Mar 12.


The Developmental Basis of Quantitative Craniofacial Variation in Humans and Mice.

Martínez-Abadías N, Mitteroecker P, Parsons TE, Esparza M, Sjøvold T, Rolian C, Richtsmeier JT, Hallgrímsson B.

Evol Biol. 2012 Dec;39(4):554-567. Epub 2012 Nov 20.


Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.

Martínez-Abadías N, Motch SM, Pankratz TL, Wang Y, Aldridge K, Jabs EW, Richtsmeier JT.

Dev Dyn. 2013 Jan;242(1):80-94. doi: 10.1002/dvdy.23903. Epub 2012 Dec 5.


A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.

Justice CM, Yagnik G, Kim Y, Peter I, Jabs EW, Erazo M, Ye X, Ainehsazan E, Shi L, Cunningham ML, Kimonis V, Roscioli T, Wall SA, Wilkie AO, Stoler J, Richtsmeier JT, Heuzé Y, Sanchez-Lara PA, Buckley MF, Druschel CM, Mills JL, Caggana M, Romitti PA, Kay DM, Senders C, Taub PJ, Klein OD, Boggan J, Zwienenberg-Lee M, Naydenov C, Kim J, Wilson AF, Boyadjiev SA.

Nat Genet. 2012 Dec;44(12):1360-4. doi: 10.1038/ng.2463. Epub 2012 Nov 18.


The skeletal site-specific role of connective tissue growth factor in prenatal osteogenesis.

Lambi AG, Pankratz TL, Mundy C, Gannon M, Barbe MF, Richtsmeier JT, Popoff SN.

Dev Dyn. 2012 Dec;241(12):1944-59. doi: 10.1002/dvdy.23888. Epub 2012 Nov 5.


The effect of a Beare-Stevenson syndrome Fgfr2 Y394C mutation on early craniofacial bone volume and relative bone mineral density in mice.

Percival CJ, Wang Y, Zhou X, Jabs EW, Richtsmeier JT.

J Anat. 2012 Nov;221(5):434-42. doi: 10.1111/j.1469-7580.2012.01555.x. Epub 2012 Aug 12.


p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.

Wang Y, Zhou X, Oberoi K, Phelps R, Couwenhoven R, Sun M, Rezza A, Holmes G, Percival CJ, Friedenthal J, Krejci P, Richtsmeier JT, Huso DL, Rendl M, Jabs EW.

J Clin Invest. 2012 Jun;122(6):2153-64. doi: 10.1172/JCI62644. Epub 2012 May 15.


Unilateral and bilateral expression of a quantitative trait: asymmetry and symmetry in coronal craniosynostosis.

Heuzé Y, Martínez-Abadías N, Stella JM, Senders CW, Boyadjiev SA, Lo LJ, Richtsmeier JT.

J Exp Zool B Mol Dev Evol. 2012 Mar;318(2):109-22. doi: 10.1002/jezb.21449.


FGF/FGFR signaling coordinates skull development by modulating magnitude of morphological integration: evidence from Apert syndrome mouse models.

Martínez-Abadías N, Heuzé Y, Wang Y, Jabs EW, Aldridge K, Richtsmeier JT.

PLoS One. 2011;6(10):e26425. doi: 10.1371/journal.pone.0026425. Epub 2011 Oct 28.


Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth.

Martínez-Abadías N, Percival C, Aldridge K, Hill CA, Ryan T, Sirivunnabood S, Wang Y, Jabs EW, Richtsmeier JT.

Dev Dyn. 2010 Nov;239(11):3058-71. doi: 10.1002/dvdy.22414.


Intracranial volume and whole brain volume in infants with unicoronal craniosynostosis.

Hill CA, Vaddi S, Moffitt A, Kane AA, Marsh JL, Panchal J, Richtsmeier JT, Aldridge K.

Cleft Palate Craniofac J. 2011 Jul;48(4):394-8. doi: 10.1597/10-051. Epub 2010 Aug 10.


Genetic and environmental contributions to variation in baboon cranial morphology.

Roseman CC, Willmore KE, Rogers J, Hildebolt C, Sadler BE, Richtsmeier JT, Cheverud JM.

Am J Phys Anthropol. 2010 Sep;143(1):1-12. doi: 10.1002/ajpa.21341.


New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis.

Heuzé Y, Boyadjiev SA, Marsh JL, Kane AA, Cherkez E, Boggan JE, Richtsmeier JT.

J Anat. 2010 Aug;217(2):85-96. doi: 10.1111/j.1469-7580.2010.01258.x. Epub 2010 Jun 22.


Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.

Wang Y, Sun M, Uhlhorn VL, Zhou X, Peter I, Martinez-Abadias N, Hill CA, Percival CJ, Richtsmeier JT, Huso DL, Jabs EW.

BMC Dev Biol. 2010 Feb 22;10:22. doi: 10.1186/1471-213X-10-22.


Brain phenotypes in two FGFR2 mouse models for Apert syndrome.

Aldridge K, Hill CA, Austin JR, Percival C, Martinez-Abadias N, Neuberger T, Wang Y, Jabs EW, Richtsmeier JT.

Dev Dyn. 2010 Mar;239(3):987-97. doi: 10.1002/dvdy.22218.

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