Richard L. Maas - Publications

Affiliations: 
Department of Medicine, Division of Genetics Harvard Medical School, Boston, MA, United States 

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Year Citation  Score
2020 Pini J, Kueper J, Hu YD, Kawasaki K, Yeung P, Tsimbal C, Yoon B, Carmichael N, Maas RL, Cotney J, Grinblat Y, Liao EC. ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration. Embo Molecular Medicine. e12013. PMID 32914578 DOI: 10.15252/Emmm.202012013  0.361
2020 Sylvester B, Brindopke F, Suzuki A, Giron M, Auslander A, Maas RL, Tsai B, Gao H, Magee W, Cox TC, Sanchez-Lara PA. A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and Palate. Genes. 11. PMID 32784565 DOI: 10.3390/Genes11080903  0.337
2019 Hu Y, Pini J, Kueper J, Agnihotri B, Maas R, Liao EC. Abstract 105: ALX1 Regulates PAX3 to Enable Cranial Neural Crest Migration During Craniofacial Development Plastic and Reconstructive Surgery. Global Open. 7: 73-74. DOI: 10.1097/01.Gox.0000558379.92935.79  0.307
2018 Nakatomi M, Ida-Yonemochi H, Nakatomi C, Saito K, Kenmotsu S, Maas RL, Ohshima H. Msx2 Prevents Stratified Squamous Epithelium Formation in the Enamel Organ. Journal of Dental Research. 97: 1355-1364. PMID 29863959 DOI: 10.1177/0022034518777746  0.318
2017 Lipskind S, Lindsey JS, Gerami-Naini B, Eaton JL, O'Connell D, Kiezun A, Ho JWK, Ng N, Parasar P, Ng M, Nickerson M, Demirci U, Maas R, Anchan RM. An Embryonic and Induced Pluripotent Stem Cell Model for Ovarian Granulosa Cell Development and Steroidogenesis. Reproductive Sciences (Thousand Oaks, Calif.). 1933719117725814. PMID 28854867 DOI: 10.1177/1933719117725814  0.367
2017 Seidel K, Marangoni P, Tang C, Houshmand B, Du W, Maas RL, Murray S, Oldham MC, Klein OD. Resolving stem and progenitor cells in the adult mouse incisor through gene co-expression analysis. Elife. 6. PMID 28475038 DOI: 10.7554/Elife.24712  0.367
2017 Seidel K, Marangoni P, Tang C, Houshmand B, Du W, Maas RL, Murray S, Oldham MC, Klein OD. Author response: Resolving stem and progenitor cells in the adult mouse incisor through gene co-expression analysis Elife. DOI: 10.7554/Elife.24712.021  0.342
2016 Rasouly HM, Kumar S, Chan S, Pisarek-Horowitz A, Sharma R, Xi QJ, Nishizaki Y, Higashi Y, Salant DJ, Maas RL, Lu W. Loss of Zeb2 in mesenchyme-derived nephrons causes primary glomerulocystic disease. Kidney International. PMID 27591083 DOI: 10.1016/J.Kint.2016.06.037  0.354
2016 Mukherjee K, Ishii K, Pillalamarri V, Kammin T, Atkin JF, Hickey SE, Xi QJ, Gusella JF, Talkowski ME, Morton CC, Maas RL, Liao EC. Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis. Human Molecular Genetics. PMID 26758871 DOI: 10.1093/Hmg/Ddw006  0.378
2015 Zhang Y, Fan J, Ho JW, Hu T, Kneeland SC, Fan X, Xi Q, Sellarole MA, de Vries WN, Lu W, Lachke SA, Lang RA, John SW, Maas RL. Crim1 regulates integrin signaling in murine lens development. Development (Cambridge, England). PMID 26681494 DOI: 10.1242/Dev.125591  0.66
2015 Faden M, AlZahrani F, Mendoza-Londono R, Dupuis L, Hartley T, Kannu P, Raiman JA, Howard A, Qin W, Tetreault M, Xi JQ, Al-Thamer I, Maas RL, Boycott K, et al. Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations. American Journal of Human Genetics. 97: 608-15. PMID 26365341 DOI: 10.1016/J.Ajhg.2015.08.007  0.373
2015 Li G, Xu F, Zhu J, Krawczyk M, Zhang Y, Yuan J, Patel S, Wang Y, Lin Y, Zhang M, Cai H, Chen D, Zhang M, Cao G, Yeh E, ... ... Maas RL, et al. Transcription factor Paired Box 6 controls limbal stem cell lineage in development and disease. The Journal of Biological Chemistry. PMID 26045558 DOI: 10.1074/Jbc.M115.662940  0.417
2015 Anchan R, Gerami-Naini B, Lindsey JS, Ho JW, Kiezun A, Lipskind S, Ng N, LiCausi JA, Kim CS, Brezina P, Tuschl T, Maas R, Kearns WG, Williams Z. Efficient differentiation of steroidogenic and germ-like cells from epigenetically-related iPSCs derived from ovarian granulosa cells. Plos One. 10: e0119275. PMID 25751620 DOI: 10.1371/Journal.Pone.0119275  0.352
2015 Quintero-Rivera F, Xi QJ, Keppler-Noreuil KM, Lee JH, Higgins AW, Anchan RM, Roberts AE, Seong IS, Fan X, Lage K, Lu LY, Tao J, Hu X, Berezney R, Gelb BD, ... ... Maas RL, et al. MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus. Human Molecular Genetics. 24: 2375-89. PMID 25574029 DOI: 10.1093/Hmg/Ddv004  0.364
2014 Anchan RM, Lachke SA, Gerami-Naini B, Lindsey J, Ng N, Naber C, Nickerson M, Cavallesco R, Rowan S, Eaton JL, Xi Q, Maas RL. Pax6- and Six3-mediated induction of lens cell fate in mouse and human ES cells. Plos One. 9: e115106. PMID 25517354 DOI: 10.1371/Journal.Pone.0115106  0.653
2014 Gfrerer L, Shubinets V, Hoyos T, Kong Y, Nguyen C, Pietschmann P, Morton CC, Maas RL, Liao EC. Functional analysis of SPECC1L in craniofacial development and oblique facial cleft pathogenesis. Plastic and Reconstructive Surgery. 134: 748-59. PMID 25357034 DOI: 10.1097/Prs.0000000000000517  0.367
2013 Coste B, Houge G, Murray MF, Stitziel N, Bandell M, Giovanni MA, Philippakis A, Hoischen A, Riemer G, Steen U, Steen VM, Mathur J, Cox J, Lebo M, Rehm H, ... ... Maas RL, et al. Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis. Proceedings of the National Academy of Sciences of the United States of America. 110: 4667-72. PMID 23487782 DOI: 10.1073/Pnas.1221400110  0.302
2012 Jumlongras D, Lachke SA, O'Connell DJ, Aboukhalil A, Li X, Choe SE, Ho JW, Turbe-Doan A, Robertson EA, Olsen BR, Bulyk ML, Amendt BA, Maas RL. An evolutionarily conserved enhancer regulates Bmp4 expression in developing incisor and limb bud. Plos One. 7: e38568. PMID 22701669 DOI: 10.1371/Journal.Pone.0038568  0.673
2012 Lachke SA, Ho JW, Kryukov GV, O'Connell DJ, Aboukhalil A, Bulyk ML, Park PJ, Maas RL. iSyTE: integrated Systems Tool for Eye gene discovery. Investigative Ophthalmology & Visual Science. 53: 1617-27. PMID 22323457 DOI: 10.1167/Iovs.11-8839  0.666
2012 O'Connell DJ, Ho JW, Mammoto T, Turbe-Doan A, O'Connell JT, Haseley PS, Koo S, Kamiya N, Ingber DE, Park PJ, Maas RL. A Wnt-bmp feedback circuit controls intertissue signaling dynamics in tooth organogenesis. Science Signaling. 5: ra4. PMID 22234613 DOI: 10.1126/Scisignal.2002414  0.372
2012 Lachke SA, Higgins AW, Inagaki M, Saadi I, Xi Q, Long M, Quade BJ, Talkowski ME, Gusella JF, Fujimoto A, Robinson ML, Yang Y, Duong QT, Shapira I, Motro B, ... ... Maas RL, et al. The cell adhesion gene PVRL3 is associated with congenital ocular defects. Human Genetics. 131: 235-50. PMID 21769484 DOI: 10.1007/S00439-011-1064-Z  0.672
2012 Shubinets V, Dougherty M, Kamel G, Morton C, Maas R, Liao E. Abstract 18: Analysis of Novel Gene Specc1L Function in Zebrafish Model of Oblique (Tessier) Facial Clefts Plastic and Reconstructive Surgery. 130: 23. DOI: 10.1097/01.Prs.0000416106.95328.95  0.327
2011 Lachke SA, Maas RL. RNA Granules and Cataract. Expert Review of Ophthalmology. 6: 497-500. PMID 23847690 DOI: 10.1586/Eop.11.53  0.568
2011 Kasaikina MV, Fomenko DE, Labunskyy VM, Lachke SA, Qiu W, Moncaster JA, Zhang J, Wojnarowicz MW, Natarajan SK, Malinouski M, Schweizer U, Tsuji PA, Carlson BA, Maas RL, Lou MF, et al. Roles of the 15-kDa selenoprotein (Sep15) in redox homeostasis and cataract development revealed by the analysis of Sep 15 knockout mice. The Journal of Biological Chemistry. 286: 33203-12. PMID 21768092 DOI: 10.1074/Jbc.M111.259218  0.633
2011 Saadi I, Alkuraya FS, Gisselbrecht SS, Goessling W, Cavallesco R, Turbe-Doan A, Petrin AL, Harris J, Siddiqui U, Grix AW, Hove HD, Leboulch P, Glover TW, Morton CC, Richieri-Costa A, ... ... Maas RL, et al. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American Journal of Human Genetics. 89: 44-55. PMID 21703590 DOI: 10.1016/J.Ajhg.2011.05.023  0.378
2011 Lachke SA, Alkuraya FS, Kneeland SC, Ohn T, Aboukhalil A, Howell GR, Saadi I, Cavallesco R, Yue Y, Tsai AC, Nair KS, Cosma MI, Smith RS, Hodges E, Alfadhli SM, ... ... Maas RL, et al. Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science (New York, N.Y.). 331: 1571-6. PMID 21436445 DOI: 10.1126/Science.1195970  0.663
2011 Anchan RM, Quaas P, Gerami-Naini B, Bartake H, Griffin A, Zhou Y, Day D, Eaton JL, George LL, Naber C, Turbe-Doan A, Park PJ, Hornstein MD, Maas RL. Amniocytes can serve a dual function as a source of iPS cells and feeder layers. Human Molecular Genetics. 20: 962-74. PMID 21156717 DOI: 10.1093/Hmg/Ddq542  0.312
2010 Lachke SA, Maas RL. Building the developmental oculome: systems biology in vertebrate eye development and disease. Wiley Interdisciplinary Reviews. Systems Biology and Medicine. 2: 305-23. PMID 20836031 DOI: 10.1002/Wsbm.59  0.628
2010 Rowan S, Siggers T, Lachke SA, Yue Y, Bulyk ML, Maas RL. Precise temporal control of the eye regulatory gene Pax6 via enhancer-binding site affinity. Genes & Development. 24: 980-5. PMID 20413611 DOI: 10.1101/Gad.1890410  0.641
2010 Nakatomi M, Wang XP, Key D, Lund JJ, Turbe-Doan A, Kist R, Aw A, Chen Y, Maas RL, Peters H. Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis. Developmental Biology. 340: 438-49. PMID 20123092 DOI: 10.1016/J.Ydbio.2010.01.031  0.43
2009 Han J, Mayo J, Xu X, Li J, Bringas P, Maas RL, Rubenstein JL, Chai Y. Indirect modulation of Shh signaling by Dlx5 affects the oral-nasal patterning of palate and rescues cleft palate in Msx1-null mice. Development (Cambridge, England). 136: 4225-33. PMID 19934017 DOI: 10.1242/Dev.036723  0.348
2009 Purcell P, Joo BW, Hu JK, Tran PV, Calicchio ML, O'Connell DJ, Maas RL, Tabin CJ. Temporomandibular joint formation requires two distinct hedgehog-dependent steps. Proceedings of the National Academy of Sciences of the United States of America. 106: 18297-302. PMID 19815519 DOI: 10.1073/Pnas.0908836106  0.362
2009 Wang XP, O'Connell DJ, Lund JJ, Saadi I, Kuraguchi M, Turbe-Doan A, Cavallesco R, Kim H, Park PJ, Harada H, Kucherlapati R, Maas RL. Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood. Development (Cambridge, England). 136: 1939-49. PMID 19429790 DOI: 10.1242/Dev.033803  0.325
2009 Rowan S, Siggers T, Lachke S, Bulyk ML, Maas RL. Prep1 regulates lens induction via direct regulation of the Pax6 ectodermal enhancer Developmental Biology. 331: 440-441. DOI: 10.1016/J.Ydbio.2009.05.199  0.624
2008 Burdon KP, Hattersley K, Lachke SA, Laurie KJ, Maas RL, Mackey DA, Craig JE. Investigation of eight candidate genes on chromosome 1p36 for autosomal dominant total congenital cataract. Molecular Vision. 14: 1799-804. PMID 18843385  0.59
2008 Rowan S, Conley KW, Le TT, Donner AL, Maas RL, Brown NL. Notch signaling regulates growth and differentiation in the mammalian lens. Developmental Biology. 321: 111-22. PMID 18588871 DOI: 10.1016/J.Ydbio.2008.06.002  0.362
2008 Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GA, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, ... ... Maas RL, et al. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. American Journal of Human Genetics. 82: 712-22. PMID 18319076 DOI: 10.1016/J.Ajhg.2008.01.011  0.324
2008 Nishimura W, Rowan S, Salameh T, Maas RL, Bonner-Weir S, Sell SM, Sharma A. Preferential reduction of beta cells derived from Pax6-MafB pathway in MafB deficient mice. Developmental Biology. 314: 443-56. PMID 18199433 DOI: 10.1016/J.Ydbio.2007.12.009  0.356
2007 Han J, Ishii M, Bringas P, Maas RL, Maxson RE, Chai Y. Concerted action of Msx1 and Msx2 in regulating cranial neural crest cell differentiation during frontal bone development. Mechanisms of Development. 124: 729-45. PMID 17693062 DOI: 10.1016/J.Mod.2007.06.006  0.373
2007 Wang XP, Suomalainen M, Felszeghy S, Zelarayan LC, Alonso MT, Plikus MV, Maas RL, Chuong CM, Schimmang T, Thesleff I. An integrated gene regulatory network controls stem cell proliferation in teeth. Plos Biology. 5: e159. PMID 17564495 DOI: 10.1371/Journal.Pbio.0050159  0.339
2007 Williamson RE, Darrow KN, Michaud S, Jacobs JS, Jones MC, Eberl DF, Maas RL, Liberman MC, Morton CC. Methylthioadenosine phosphorylase (MTAP) in hearing: gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis. American Journal of Medical Genetics. Part A. 143: 1630-9. PMID 17534888 DOI: 10.1002/Ajmg.A.31724  0.327
2007 Lu W, Quintero-Rivera F, Fan Y, Alkuraya FS, Donovan DJ, Xi Q, Turbe-Doan A, Li QG, Campbell CG, Shanske AL, Sherr EH, Ahmad A, Peters R, Rilliet B, Parvex P, ... ... Maas RL, et al. NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. Plos Genetics. 3: e80. PMID 17530927 DOI: 10.1371/Journal.Pgen.0030080  0.366
2007 Lu W, van Eerde AM, Fan X, Quintero-Rivera F, Kulkarni S, Ferguson H, Kim HG, Fan Y, Xi Q, Li QG, Sanlaville D, Andrews W, Sundaresan V, Bi W, Yan J, ... ... Maas RL, et al. Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. American Journal of Human Genetics. 80: 616-32. PMID 17357069 DOI: 10.1086/512735  0.339
2007 Donner AL, Ko F, Episkopou V, Maas RL. Pax6 is misexpressed in Sox1 null lens fiber cells. Gene Expression Patterns : Gep. 7: 606-13. PMID 17306631 DOI: 10.1016/J.Modgep.2007.01.001  0.325
2007 Donner AL, Episkopou V, Maas RL. Sox2 and Pou2f1 interact to control lens and olfactory placode development. Developmental Biology. 303: 784-99. PMID 17140559 DOI: 10.1016/J.Ydbio.2006.10.047  0.432
2007 Lu W, Eerde Av, Fan X, Quintero-Rivera F, Li Q, Sanlaville D, Andrews W, Sundaresan V, Giltay J, Feather S, Woolf A, Rao Y, Morton C, Maas R. 128: Disruption of ROBO2 is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux American Journal of Kidney Diseases. 49. DOI: 10.1053/J.Ajkd.2007.02.134  0.339
2006 Donner AL, Lachke SA, Maas RL. Lens induction in vertebrates: variations on a conserved theme of signaling events. Seminars in Cell & Developmental Biology. 17: 676-85. PMID 17164096 DOI: 10.1016/J.Semcdb.2006.10.005  0.614
2006 Zhang X, Rowan S, Yue Y, Heaney S, Pan Y, Brendolan A, Selleri L, Maas RL. Pax6 is regulated by Meis and Pbx homeoproteins during pancreatic development. Developmental Biology. 300: 748-57. PMID 17049510 DOI: 10.1016/J.Ydbio.2006.06.030  0.361
2006 Nolte C, Rastegar M, Amores A, Bouchard M, Grote D, Maas R, Kovacs EN, Postlethwait J, Rambaldi I, Rowan S, Yan YL, Zhang F, Featherstone M. Stereospecificity and PAX6 function direct Hoxd4 neural enhancer activity along the antero-posterior axis. Developmental Biology. 299: 582-93. PMID 17010333 DOI: 10.1016/J.Ydbio.2006.08.061  0.346
2006 Kuraguchi M, Wang XP, Bronson RT, Rothenberg R, Ohene-Baah NY, Lund JJ, Kucherlapati M, Maas RL, Kucherlapati R. Adenomatous polyposis coli (APC) is required for normal development of skin and thymus. Plos Genetics. 2: e146. PMID 17002498 DOI: 10.1371/Journal.Pgen.0020146  0.369
2006 Alkuraya FS, Saadi I, Lund JJ, Turbe-Doan A, Morton CC, Maas RL. SUMO1 haploinsufficiency leads to cleft lip and palate. Science (New York, N.Y.). 313: 1751. PMID 16990542 DOI: 10.1126/Science.1128406  0.378
2005 Purcell P, Oliver G, Mardon G, Donner AL, Maas RL. Pax6-dependence of Six3, Eya1 and Dach1 expression during lens and nasal placode induction. Gene Expression Patterns : Gep. 6: 110-8. PMID 16024294 DOI: 10.1016/J.Modgep.2005.04.010  0.423
2004 Donner AL, Maas RL. Conservation and non-conservation of genetic pathways in eye specification. The International Journal of Developmental Biology. 48: 743-53. PMID 15558467 DOI: 10.1387/Ijdb.041877Ad  0.348
2004 Bei M, Stowell S, Maas R. Msx2 controls ameloblast terminal differentiation Developmental Dynamics. 231: 758-765. PMID 15499554 DOI: 10.1002/Dvdy.20182  0.397
2004 Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia. Human Genetics. 114: 242-9. PMID 14689302 DOI: 10.1007/S00439-003-1066-6  0.478
2003 Li X, Oghi KA, Zhang J, Krones A, Bush KT, Glass CK, Nigam SK, Aggarwal AK, Maas R, Rose DW, Rosenfeld MG. Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis. Nature. 426: 247-54. PMID 14628042 DOI: 10.1038/Nature02083  0.38
2003 Han J, Ito Y, Yeo JY, Sucov HM, Maas R, Chai Y. Cranial neural crest-derived mesenchymal proliferation is regulated by Msx1-mediated p19(INK4d) expression during odontogenesis. Developmental Biology. 261: 183-96. PMID 12941628 DOI: 10.1016/S0012-1606(03)00300-2  0.398
2003 Yao MW, Lim H, Schust DJ, Choe SE, Farago A, Ding Y, Michaud S, Church GM, Maas RL. Gene expression profiling reveals progesterone-mediated cell cycle and immunoregulatory roles of Hoxa-10 in the preimplantation uterus. Molecular Endocrinology (Baltimore, Md.). 17: 610-27. PMID 12554760 DOI: 10.1210/Me.2002-0290  0.383
2003 Zhang X, Heaney S, Maas RL. Cre-loxp fate-mapping of Pax6 enhancer active retinal and pancreatic progenitors. Genesis (New York, N.Y. : 2000). 35: 22-30. PMID 12481295 DOI: 10.1002/Gene.10160  0.373
2002 Leader B, Lim H, Carabatsos MJ, Harrington A, Ecsedy J, Pellman D, Maas R, Leder P. Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouse oocytes. Nature Cell Biology. 4: 921-8. PMID 12447394 DOI: 10.1038/Ncb880  0.747
2002 Gritli-Linde A, Bei M, Maas R, Zhang XM, Linde A, McMahon AP. Shh signaling within the dental epithelium is necessary for cell proliferation, growth and polarization. Development (Cambridge, England). 129: 5323-37. PMID 12403705 DOI: 10.1242/Dev.00100  0.343
2002 Zhang X, Friedman A, Heaney S, Purcell P, Maas RL. Meis homeoproteins directly regulate Pax6 during vertebrate lens morphogenesis. Genes & Development. 16: 2097-107. PMID 12183364 DOI: 10.1101/Gad.1007602  0.425
2001 Couse JF, Dixon D, Yates M, Moore AB, Ma L, Maas R, Korach KS. Estrogen receptor-alpha knockout mice exhibit resistance to the developmental effects of neonatal diethylstilbestrol exposure on the female reproductive tract. Developmental Biology. 238: 224-38. PMID 11784006 DOI: 10.1006/Dbio.2001.0413  0.313
2001 Munnia A, Schütz N, Romeike BFM, Maldener E, Glass B, Maas R, Nastainczyk W, Feiden W, Fischer U, Meese E. Expression, cellular distribution and protein binding of the glioma amplified sequence (GAS41), a highly conserved putative transcription factor. Oncogene. 20: 4853-4863. PMID 11521196 DOI: 10.1038/Sj.Onc.1204650  0.331
2001 Jumlongras D, Bei M, Stimson JM, Wang WF, DePalma SR, Seidman CE, Felbor U, Maas R, Seidman JG, Olsen BR. A nonsense mutation in MSX1 causes Witkop syndrome. American Journal of Human Genetics. 69: 67-74. PMID 11369996 DOI: 10.1086/321271  0.526
2001 Davis RJ, Shen W, Sandler YI, Amoui M, Purcell P, Maas R, Ou CN, Vogel H, Beaudet AL, Mardon G. Dach1 mutant mice bear no gross abnormalities in eye, limb, and brain development and exhibit postnatal lethality. Molecular and Cellular Biology. 21: 1484-90. PMID 11238885 DOI: 10.1128/Mcb.21.5.1484-1490.2001  0.39
2000 Chen Y, Zhang Y, Jiang TX, Barlow AJ, St Amand TR, Hu Y, Heaney S, Francis-West P, Chuong CM, Maas R. Conservation of early odontogenic signaling pathways in Aves. Proceedings of the National Academy of Sciences of the United States of America. 97: 10044-9. PMID 10954731 DOI: 10.1073/Pnas.160245097  0.382
2000 Branford WW, Benson GV, Ma L, Maas RL, Potter SS. Characterization of Hoxa-10/Hoxa-11 transheterozygotes reveals functional redundancy and regulatory interactions. Developmental Biology. 224: 373-87. PMID 10926774 DOI: 10.1006/Dbio.2000.9809  0.404
2000 Sivak JM, Mohan R, Rinehart WB, Xu PX, Maas RL, Fini ME. Pax-6 expression and activity are induced in the reepithelializing cornea and control activity of the transcriptional promoter for matrix metalloproteinase gelatinase B. Developmental Biology. 222: 41-54. PMID 10885745 DOI: 10.1006/Dbio.2000.9694  0.382
2000 Wawersik S, Maas RL. Vertebrate eye development as modeled in Drosophila Human Molecular Genetics. 9: 917-925. PMID 10767315 DOI: 10.1093/Hmg/9.6.917  0.361
2000 Satokata I, Ma L, Ohshima H, Bei M, Woo I, Nishizawa K, Maeda T, Takano Y, Uchiyama M, Heaney S, Peters H, Tang Z, Maxson R, Maas R. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nature Genetics. 24: 391-5. PMID 10742104 DOI: 10.1038/74231  0.387
1999 Ma L, Yao M, Maas RL. Genetic control of uterine receptivity during implantation. Seminars in Reproductive Endocrinology. 17: 205-216. PMID 10797939 DOI: 10.1055/S-2007-1016228  0.307
1999 Lim H, Ma L, Ma WG, Maas RL, Dey SK. Hoxa-10 regulates uterine stromal cell responsiveness to progesterone during implantation and decidualization in the mouse. Molecular Endocrinology (Baltimore, Md.). 13: 1005-17. PMID 10379898 DOI: 10.1210/Mend.13.6.0284  0.404
1999 Wawersik S, Purcell P, Rauchman M, Dudley AT, Robertson EJ, Maas R. BMP7 acts in murine lens placode development. Developmental Biology. 207: 176-188. PMID 10049573 DOI: 10.1006/Dbio.1998.9153  0.417
1999 Podlasek CA, Seo RM, Clemens JQ, Ma L, Maas RL, Bushman W. Hoxa-10 deficient male mice exhibit abnormal development of the accessory sex organs. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 214: 1-12. PMID 9915571 DOI: 10.1002/(Sici)1097-0177(199901)214:1<1::Aid-Dvdy1>3.0.Co;2-2  0.381
1998 Jain MK, Kashiki S, Hsieh CM, Layne MD, Yet SF, Sibinga NE, Chin MT, Feinberg MW, Woo I, Maas RL, Haber E, Lee ME. Embryonic expression suggests an important role for CRP2/SmLIM in the developing cardiovascular system. Circulation Research. 83: 980-5. PMID 9815145 DOI: 10.1161/01.Res.83.10.980  0.347
1998 Ma L, Benson GV, Lim H, Dey SK, Maas RL. Abdominal B (AbdB) Hoxa genes: regulation in adult uterus by estrogen and progesterone and repression in müllerian duct by the synthetic estrogen diethylstilbestrol (DES). Developmental Biology. 197: 141-54. PMID 9630742 DOI: 10.1006/Dbio.1998.8907  0.392
1998 Sharon-Friling R, Richardson J, Sperbeck S, Lee D, Rauchman M, Maas R, Swaroop A, Wistow G. Lens-specific gene recruitment of zeta-crystallin through Pax6, Nrl-Maf, and brain suppressor sites. Molecular and Cellular Biology. 18: 2067-76. PMID 9528779 DOI: 10.1128/Mcb.18.4.2067  0.35
1997 Xu PX, Cheng J, Epstein JA, Maas RL. Mouse Eya genes are expressed during limb tendon development and encode a transcriptional activation function. Proceedings of the National Academy of Sciences of the United States of America. 94: 11974-9. PMID 9342347 DOI: 10.1073/Pnas.94.22.11974  0.422
1997 Maas R, Bei M. The Genetic Control of Early Tooth Development Critical Reviews in Oral Biology & Medicine. 8: 4-39. PMID 9063623 DOI: 10.1177/10454411970080010101  0.412
1996 Maas R, Chen YP, Bei M, Woo I, Satokata I. The role of Msx genes in mammalian development. Annals of the New York Academy of Sciences. 785: 171-81. PMID 8702124 DOI: 10.1111/J.1749-6632.1996.Tb56256.X  0.35
1996 Epstein JA, Shapiro DN, Cheng J, Lam PY, Maas RL. Pax3 modulates expression of the c-Met receptor during limb muscle development. Proceedings of the National Academy of Sciences of the United States of America. 93: 4213-8. PMID 8633043 DOI: 10.1073/Pnas.93.9.4213  0.338
1995 Benson GV, Nguyen T-E, Maas RL. The expression pattern of the murine Hoxa-10 gene and the sequence recognition of its homeodomain reveal specific properties of Abdominal B-like genes. Molecular and Cellular Biology. 15: 1591-1601. PMID 7862151 DOI: 10.1128/Mcb.15.3.1591  0.364
1995 Epstein JA, Lam P, Jepeal L, Maas RL, Shapiro DN. Pax3 inhibits myogenic differentiation of cultured myoblast cells. The Journal of Biological Chemistry. 270: 11719-22. PMID 7744814 DOI: 10.1074/Jbc.270.20.11719  0.362
1995 Satokata I, Benson G, Maas R. Sexually dimorphic sterility phenotypes in HoxalO-deficient mice Nature. 374: 460-463. PMID 7700356 DOI: 10.1038/374460A0  0.393
1994 Glaser T, Ton CC, Mueller R, Petzl-Erler ML, Oliver C, Nevin NC, Housman DE, Maas RL. Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation). Genomics. 19: 145-8. PMID 8188215 DOI: 10.1006/Geno.1994.1024  0.34
1994 Epstein JA, Glaser T, Cai J, Jepeal L, Walton DS, Maas RL. Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing Genes and Development. 8: 2022-2034. PMID 7958875 DOI: 10.1101/Gad.8.17.2022  0.306
1994 Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nature Genetics. 7: 463-71. PMID 7951315 DOI: 10.1038/Ng0894-463  0.39
1994 Satokata I, Maas R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development Nature Genetics. 6: 348-356. PMID 7914451 DOI: 10.1038/Ng0494-348  0.376
1994 Maas R, Elfering S, Glaser T, Jepeal L. Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation. Developmental Dynamics. 199: 214-228. PMID 7517224 DOI: 10.1002/Aja.1001990306  0.327
1992 Glaser T, Walton DS, Maas RL. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene Nature Genetics. 2: 232-239. PMID 1345175 DOI: 10.1038/Ng1192-232  0.384
1990 Woychik RP, Maas RL, Zeller R, Vogt TF, Leder P. 'Formins': proteins deduced from the alternative transcripts of the limb deformity gene. Nature. 346: 850-3. PMID 2392150 DOI: 10.1038/346850A0  0.568
Low-probability matches (unlikely to be authored by this person)
2016 Lin H, Ouyang H, Zhu J, Huang S, Liu Z, Chen S, Cao G, Li G, Signer RA, Xu Y, Chung C, Zhang Y, Lin D, Patel S, Wu F, ... ... Maas RL, et al. Lens regeneration using endogenous stem cells with gain of visual function. Nature. PMID 26958831 DOI: 10.1038/Nature17181  0.299
2003 Ma L, Liu J, Wu T, Plikus M, Jiang TX, Bi Q, Liu YH, Müller-Röver S, Peters H, Sundberg JP, Maxson R, Maas RL, Chuong CM. 'Cyclic alopecia' in Msx2 mutants: defects in hair cycling and hair shaft differentiation. Development (Cambridge, England). 130: 379-89. PMID 12466204 DOI: 10.1242/Dev.00201  0.298
2015 Chopra SS, Leshchiner I, Duzkale H, McLaughlin H, Giovanni M, Zhang C, Stitziel N, Fingeroth J, Joyce RM, Lebo M, Rehm H, Vuzman D, Maas R, Sunyaev SR, Murray M, et al. Inherited CHST11/MIR3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease. Molecular Genetics & Genomic Medicine. 3: 413-23. PMID 26436107 DOI: 10.1002/Mgg3.152  0.292
2007 Leach NT, Sun Y, Michaud S, Zheng Y, Ligon KL, Ligon AH, Sander T, Korf BR, Lu W, Harris DJ, Gusella JF, Maas RL, Quade BJ, Cole AJ, Kelz MB, et al. Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice. American Journal of Human Genetics. 80: 792-9. PMID 17357084 DOI: 10.1086/513019  0.285
2014 Campàs O, Mammoto T, Hasso S, Sperling RA, O'Connell D, Bischof AG, Maas R, Weitz DA, Mahadevan L, Ingber DE. Quantifying cell-generated mechanical forces within living embryonic tissues. Nature Methods. 11: 183-9. PMID 24317254 DOI: 10.1038/Nmeth.2761  0.284
2019 Kueper J, Pini J, Hu YD, Sobti N, Rebello M, Ishii K, Carmichael N, Perroni V, Maas RL, Grinblatt Y, Liao EC. Abstract 7: Novel Stem Cell Model of Frontonasal Dysplasia derived from Pedigree with ALX1-Mutation Plastic and Reconstructive Surgery. Global Open. 7: 5-6. DOI: 10.1097/01.Gox.0000558281.15437.Cd  0.282
2002 Xu PX, Zheng W, Laclef C, Maire P, Maas RL, Peters H, Xu X. Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid. Development (Cambridge, England). 129: 3033-44. PMID 12070080  0.275
2018 Haghighi A, Krier JB, Toth-Petroczy A, Cassa CA, Frank NY, Carmichael N, Fieg E, Bjonnes A, Mohanty A, Briere LC, Lincoln S, Lucia S, Gupta VA, Söylemez O, Sutti S, ... ... Maas RL, et al. An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery. Npj Genomic Medicine. 3: 21. PMID 30131872 DOI: 10.1038/S41525-018-0060-9  0.273
2012 Nusinow DP, Kiezun A, O'Connell DJ, Chick JM, Yue Y, Maas RL, Gygi SP, Sunyaev SR. Network-based inference from complex proteomic mixtures using SNIPE. Bioinformatics (Oxford, England). 28: 3115-22. PMID 23060611 DOI: 10.1093/Bioinformatics/Bts594  0.273
2016 Brinkley JF, Fisher S, Harris MP, Holmes G, Hooper JE, Jabs EW, Jones KL, Kesselman C, Klein OD, Maas RL, Marazita ML, Selleri L, Spritz RA, van Bakel H, Visel A, et al. The FaceBase Consortium: A comprehensive resource for craniofacial researchers. Development (Cambridge, England). PMID 27287806 DOI: 10.1242/Dev.135434  0.272
2004 Li X, Ohgi KA, Zhang J, Krones A, Bush KT, Glass CK, Nigam SK, Aggarwal AK, Maas R, Rose DW, Rosenfeld MG. Erratum: Corrigendum: Eya protein phosphatase activity regulates Six1–Dach–Eya transcriptional effects in mammalian organogenesis Nature. 427: 265-265. DOI: 10.1038/Nature02283  0.27
2018 Li G, Martínez-Bonet M, Wu D, Yang Y, Cui J, Nguyen HN, Cunin P, Levescot A, Bai M, Westra HJ, Okada Y, Brenner MB, Raychaudhuri S, Hendrickson EA, Maas RL, et al. High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction. Nature Genetics. PMID 30013183 DOI: 10.1038/S41588-018-0159-Z  0.27
1999 Xu HE, Rould MA, Xu W, Epstein JA, Maas RL, Pabo CO. Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding. Genes & Development. 13: 1263-75. PMID 10346815 DOI: 10.1101/Gad.13.10.1263  0.27
2016 Rebustini IT, Vlahos M, Packer T, Kukuruzinska MA, Maas RL. An integrated miRNA functional screening and target validation method for organ morphogenesis. Scientific Reports. 6: 23215. PMID 26980315 DOI: 10.1038/Srep23215  0.262
2008 Kirchhoff F, Krebs C, Abdulhag UN, Meyer-Schwesinger C, Maas R, Helmchen U, Hilgers KF, Wolf G, Stahl RA, Wenzel U. Rapid development of severe end-organ damage in C57BL/6 mice by combining DOCA salt and angiotensin II. Kidney International. 73: 643-50. PMID 18033241 DOI: 10.1038/Sj.Ki.5002689  0.257
1996 Maas R. Keeping an eye on eye development. Nature Genetics. 12: 346-347. PMID 8630480 DOI: 10.1038/Ng0496-346  0.256
2018 Kelsen JR, Ouahed J, Spessott WA, Kooshesh K, Sanmillan ML, Dawany N, Sullivan KE, Hamilton K, Slowik V, Nejentsev S, Farela Neves J, Flores H, Chung WK, Wilson A, Yeboa KA, ... ... Maas RL, et al. 25 MUTATIONS IN STXBP3 CONTRIBUTE TO VERY EARLY ONSET OF IBD, IMMUNODEFICIENCY AND HEARING LOSS Gastroenterology. 154: S40-S41. DOI: 10.1053/J.Gastro.2017.11.120  0.256
2013 Arbab M, Mahony S, Cho H, Chick JM, Rolfe PA, van Hoff JP, Morris VW, Gygi SP, Maas RL, Gifford DK, Sherwood RI. A multi-parametric flow cytometric assay to analyze DNA-protein interactions. Nucleic Acids Research. 41: e38. PMID 23143268 DOI: 10.1093/Nar/Gks1034  0.255
1999 Xu PX, Adams J, Peters H, Brown MC, Heaney S, Maas R. Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia Nature Genetics. 23: 113-117. PMID 10471511 DOI: 10.1038/12722  0.247
2012 Zhang X, Khimji I, Shao L, Safaee H, Desai K, Keles HO, Gurkan UA, Kayaalp E, Nureddin A, Anchan RM, Maas RL, Demirci U. Nanoliter droplet vitrification for oocyte cryopreservation. Nanomedicine (London, England). 7: 553-64. PMID 22188180 DOI: 10.2217/Nnm.11.145  0.246
2008 Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GAP, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, ... ... Maas RL, et al. Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project (DOI:10.1016/j.ajhg.2008.01.011) American Journal of Human Genetics. 83: 425-427. DOI: 10.1016/J.Ajhg.2008.08.011  0.244
2013 Gfrerer L, Shubinets V, Morton C, Maas R, Liao E. LOP16: Analysis of SPECC1L in Zebrafish model of oblique (tessier) facial clefts Plastic and Reconstructive Surgery. 132: 502. DOI: 10.1097/01.Prs.0000433347.44099.De  0.243
2008 Wang X, O'Connell D, Lund JJ, Saadi I, Kuraguchi M, Turbe-Doan A, Kucherlapati R, Maas RL. APC inhibits supernumerary tooth formation during embryogenesis and throughout adulthood Developmental Biology. 319: 480. DOI: 10.1016/J.Ydbio.2008.05.054  0.242
2020 Samuels BD, Aho R, Brinkley JF, Bugacov A, Feingold E, Fisher S, Gonzalez-Reiche AS, Hacia JG, Hallgrimsson B, Hansen K, Harris MP, Ho TV, Holmes G, Hooper JE, Jabs EW, ... ... Maas RL, et al. FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research. Development (Cambridge, England). 147. PMID 32958507 DOI: 10.1242/Dev.191213  0.24
2014 Gfrerer L, Shubinets V, Nguyen C, Morton CC, Maas RL, Liao EC. Abstract 14: requirement of specc1lb in facial prominence integration and formation of the lower jaw. Plastic and Reconstructive Surgery. 133: 24. PMID 25942125 DOI: 10.1097/01.Prs.0000445007.18495.25  0.24
2014 Campàs O, Mammoto T, Hasso S, Sperling RA, O'Connell D, Bischof AG, Maas R, Weitz DA, Mahadevan L, Ingber DE. Corrigendum: Quantifying cell-generated mechanical forces within living embryonic tissues Nature Methods. 11: 349. DOI: 10.1038/Nmeth0314-349D  0.238
2016 Lin H, Ouyang H, Zhu J, Huang S, Liu Z, Chen S, Cao G, Li G, Signer RA, Xu Y, Chung C, Zhang Y, Lin D, Patel S, Wu F, ... ... Maas RL, et al. Corrigendum: Lens regeneration using endogenous stem cells with gain of visual function. Nature. PMID 27919080 DOI: 10.1038/Nature19831  0.236
2000 Wawersik S, Purcell P, Maas RL. Pax6 and the genetic control of early eye development. Results and Problems in Cell Differentiation. 31: 15-36. PMID 10929399 DOI: 10.1007/978-3-540-46826-4_2  0.233
1994 Barnett JV, Moustakas A, Lin W, Wang XF, Lin HY, Galper JB, Maas RL. Cloning and developmental expression of the chick type II and type III TGF beta receptors. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 199: 12-27. PMID 8167376 DOI: 10.1002/Aja.1001990103  0.231
2020 Zhang Y, Guillermier C, De Raedt T, Cox AG, Maertens O, Yimlamai D, Lun M, Whitney A, Maas RL, Goessling W, Cichowski K, Steinhauser ML. Imaging Mass Spectrometry Reveals Tumor Metabolic Heterogeneity. Iscience. 23: 101355. PMID 32712466 DOI: 10.1016/J.Isci.2020.101355  0.231
2015 Cassa CA, Smith SE, Docken W, Hoffman E, McLaughlin H, Chun S, Leshchiner I, Miraoui H, Raychaudhuri S, Frank NY, Wilson BJ, Sunyaev SR, Maas RL, Vuzman D. An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood. Rheumatology (Oxford, England). PMID 26493744 DOI: 10.1093/Rheumatology/Kev367  0.222
2015 Li CC, Kharaziha M, Min C, Maas R, Nikkhah M. Microfabrication of Cell-Laden Hydrogels for Engineering Mineralized and Load Bearing Tissues. Advances in Experimental Medicine and Biology. 881: 15-31. PMID 26545742 DOI: 10.1007/978-3-319-22345-2_2  0.221
2013 Tasoglu S, Safaee H, Zhang X, Kingsley JL, Catalano PN, Gurkan UA, Nureddin A, Kayaalp E, Anchan RM, Maas RL, Tüzel E, Demirci U. Exhaustion of racing sperm in nature-mimicking microfluidic channels during sorting. Small (Weinheim An Der Bergstrasse, Germany). 9: 3374-84. PMID 23677651 DOI: 10.1002/Smll.201300020  0.218
1983 Maas RL, Brash AR. Evidence for a lipoxygenase mechanism in the biosynthesis of epoxide and dihydroxy leukotrienes from 15(S)-hydroperoxyicosatetraenoic acid by human platelets and porcine leukocytes. Proceedings of the National Academy of Sciences of the United States of America. 80: 2884-8. PMID 6304687 DOI: 10.1073/Pnas.80.10.2884  0.211
1981 Fitzgerald GA, Maas RL, Stein R, Oates JA, Roberts LJ. Intravenous prostacyclin in thrombotic thrombocytopenic purpura. Annals of Internal Medicine. 95: 319-22. PMID 7023309 DOI: 10.7326/0003-4819-95-3-319  0.21
1983 FitzGerald GA, Oates JA, Hawiger J, Maas RL, Roberts LJ, Lawson JA, Brash AR. Endogenous biosynthesis of prostacyclin and thromboxane and platelet function during chronic administration of aspirin in man. The Journal of Clinical Investigation. 71: 676-88. PMID 6338043 DOI: 10.1172/Jci110814  0.208
2002 Kwang SJ, Brugger SM, Lazik A, Merrill AE, Wu LY, Liu YH, Ishii M, Sangiorgi FO, Rauchman M, Sucov HM, Maas RL, Maxson RE. Msx2 is an immediate downstream effector of Pax3 in the development of the murine cardiac neural crest. Development (Cambridge, England). 129: 527-38. PMID 11807043  0.207
2010 Song YS, Adler D, Xu F, Kayaalp E, Nureddin A, Anchan RM, Maas RL, Demirci U. Vitrification and levitation of a liquid droplet on liquid nitrogen. Proceedings of the National Academy of Sciences of the United States of America. 107: 4596-600. PMID 20176969 DOI: 10.1073/Pnas.0914059107  0.198
1982 Maas RL, Brash AR, Oates JA. A second pathway of leukotriene biosynthesis in porcine leukocytes. Proceedings of the National Academy of Sciences of the United States of America. 78: 5523-27. PMID 6272308 DOI: 10.1073/Pnas.78.9.5523  0.198
1990 Maas R. Book Review Principles of Medical Genetics By Thomas D. Gelehrter and Francis S. Collins. 324 pp., illustrated. Baltimore, Williams and Wilkins, 1990. $34.95. The New England Journal of Medicine. 323: 1285-1285. DOI: 10.1056/Nejm199011013231819  0.194
2013 Tasoglu S, Safaee H, Zhang X, Kingsley JL, Catalano PN, Gurkan UA, Nureddin A, Kayaalp E, Anchan RM, Maas RL, Tüzel E, Demirci U. Microfluidic Sorting: Exhaustion of Racing Sperm in Nature-Mimicking Microfluidic Channels During Sorting (Small 20/2013) Small. 9: 3366-3366. DOI: 10.1002/Smll.201370121  0.191
2003 Desai S, Wang DQ, Maas RL. Pax6 is reactivated druing pancreatic inflammation Gastroenterology. 124. DOI: 10.1016/S0016-5085(03)82954-2  0.19
1981 Robertson RM, Robertson D, Roberts LJ, Maas RL, FitzGerald GA, Friesinger GC, Oates JA. Thromboxane A2 in vasotonic angina pectoris: evidence from direct measurements and inhibitor trials. The New England Journal of Medicine. 304: 998-1003. PMID 7010173 DOI: 10.1056/Nejm198104233041703  0.187
2009 Song YS, Adler D, Keles HO, Kayaalp E, Nureddin A, Anchan RM, Maas R, Demirci U. 40. Levitating vitrified droplets Cryobiology. 59: 381. DOI: 10.1016/J.Cryobiol.2009.10.054  0.184
2015 Rochard LJ, Li E, Nguyen C, Gusella JF, Maas R, Morton C, Talkowski M, Liao EC. Abstract 91 Plastic and Reconstructive Surgery. 135: 68. DOI: 10.1097/01.Prs.0000465539.66357.B4  0.177
2015 Mukherjee K, Ishii K, Grimaldi MJ, Nguyen C, Talkowski M, Gusella J, Maas R, Morton CC, Liao EC. Abstract 74 Plastic and Reconstructive Surgery. 135: 57-58. DOI: 10.1097/01.Prs.0000465522.30918.E9  0.177
2022 Pini J, Kueper J, Hu YD, Kawasaki K, Yeung P, Tsimbal C, Yoon B, Carmichael N, Maas RL, Cotney J, Grinblat Y, Liao EC. ALX1-related frontonasal dysplasia results from defective neural crest cell development and migration. Embo Molecular Medicine. 14: e16289. PMID 35795978 DOI: 10.15252/emmm.202216289  0.171
2009 Anchan R, Lachke S, Gerami-Naini B, Naber K, Eaton J, Maas R. Transcription factor directed differentiation of embryonic stem cells in vitro Fertility and Sterility. 92: S172. DOI: 10.1016/J.Fertnstert.2009.07.1334  0.166
2020 Bendapudi P, Ryu J, Soylemez O, Rouaisnel B, Colling M, Pasko B, Robbins A, Bouzinier M, Tomczak L, Ram S, Toth-Petroczy A, Krier J, Fieg E, Dzik W, Hudspeth J, ... ... Maas R, et al. Rare Inherited Defects of the Complement System in Purpura Fulminans Blood. 136: 35-36. DOI: 10.1182/blood-2020-138729  0.162
2023 Bendapudi PK, Nazeen S, Ryu J, Soylemez O, Robbins AK, Rouaisnel B, O'Neil JK, Pokhriyal R, Yang M, Colling M, Pasko B, Bouzinier M, Tomczak L, Collier L, Barrios DA, ... ... Maas R, et al. Low-frequency inherited complement receptor variants are associated with purpura fulminans. Blood. PMID 38096369 DOI: 10.1182/blood.2023021231  0.12
2018 Kelsen JR, Ouahed J, Spessott WA, Kooshesh K, Sanmillan ML, Dawany N, Sullivan KE, Hamilton K, Slowik V, Nejentsev S, Neves JF, Flores H, Chung WK, Wilson A, Yeboa KA, ... ... Maas RL, et al. 25 MUTATIONS IN STXBP3 CONTRIBUTE TO VERY EARLY ONSET OF IBD, IMMUNODEFICIENCY AND HEARING LOSS Inflammatory Bowel Diseases. 24: S28-S28. DOI: 10.1093/ibd/izy019.087  0.112
2022 David L, Martinez L, Xi Q, Kooshesh KA, Zhang Y, Shah JV, Maas RL, Wu H. Piezo mechanosensory channels regulate centrosome integrity and mitotic entry. Proceedings of the National Academy of Sciences of the United States of America. 120: e2213846120. PMID 36574677 DOI: 10.1073/pnas.2213846120  0.107
2018 Bugiardini E, Phadke R, Maas R, Pittman A, Kusters B, Morrow J, Parton M, Nunes A, Akhtar M, Syrris P, Lopes L, Fotelonga T, Houlden H, Elliott P, Hanna M, et al. CONGENITAL MUSCULAR DYSTROPHIES Neuromuscular Disorders. 28: S131. DOI: 10.1016/j.nmd.2018.06.382  0.099
2021 Ouahed J, Kelsen JR, Spessott WA, Kooshesh K, Sanmillan ML, Dawany N, Sullivan KE, Hamilton K, Slowik V, Nejentsev S, Neves JF, Flores H, Chung WK, Wilson A, Yeboa KA, ... ... Maas RL, et al. Variants in STXBP3 Are Associated With Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation. Journal of Crohn's & Colitis. PMID 33891011 DOI: 10.1093/ecco-jcc/jjab077  0.098
1994 Epstein J, Cai J, Glaser T, Jepeal L, Maas R. Identification of a Pax paired domain recognition sequence and evidence for DNA-dependent conformational changes. Journal of Biological Chemistry. 269: 8355-8361. DOI: 10.1016/s0021-9258(17)37201-0  0.065
1999 Maas R. Humans as Model Organisms Cell. 96: 455-456. DOI: 10.1016/S0092-8674(00)80633-9  0.062
2018 Liu Y, Granet D, Lin H, Baxter S, Ouyang H, Zhu J, Huang S, Liu Z, Wu X, Yan F, Liu X, Luo L, Heichel C, Zhang M, Cai W, ... Maas RL, et al. Liu et al. reply. Nature. 556: E3-E4. PMID 29620731 DOI: 10.1038/nature26150  0.01
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