| THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia PV Tran, CJ Haycraft, TY Besschetnova, A Turbe-Doan, RW Stottmann, ... Nature genetics 40 (4), 403-410, 2008 | 371 | 2008 |
| Chordin and noggin promote organizing centers of forebrain development in the mouse RM Anderson, AR Lawrence, RW Stottmann, D Bachiller, J Klingensmith Oxford University Press for The Company of Biologists Limited 129 (21), 4975 …, 2002 | 257 | 2002 |
| BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium RW Stottmann, M Choi, Y Mishina, EN Meyers, J Klingensmith Oxford University Press for The Company of Biologists Limited 131 (9), 2205-2218, 2004 | 228 | 2004 |
| The BMP antagonists Chordin and Noggin have essential but redundant roles in mouse mandibular outgrowth RW Stottmann, RM Anderson, J Klingensmith Developmental biology 240 (2), 457-473, 2001 | 158 | 2001 |
| Mutation mapping and identification by whole-genome sequencing I Leshchiner, K Alexa, P Kelsey, I Adzhubei, CA Austin-Tse, JD Cooney, ... Genome research 22 (8), 1541-1548, 2012 | 151 | 2012 |
| Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain RW Stottmann, PV Tran, A Turbe-Doan, DR Beier Developmental biology 335 (1), 166-178, 2009 | 95 | 2009 |
| The BMP antagonist Noggin promotes cranial and spinal neurulation by distinct mechanisms RW Stottmann, M Berrong, K Matta, M Choi, J Klingensmith Developmental biology 295 (2), 647-663, 2006 | 93 | 2006 |
| The bone morphogenetic protein antagonist noggin regulates mammalian cardiac morphogenesis M Choi, RW Stottmann, YP Yang, EN Meyers, J Klingensmith Circulation research 100 (2), 220-228, 2007 | 80 | 2007 |
| Endogenous bone morphogenetic protein antagonists regulate mammalian neural crest generation and survival RM Anderson, RW Stottmann, M Choi, J Klingensmith Developmental dynamics: an official publication of the American Association …, 2006 | 70 | 2006 |
| A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice Z Abdelhamed, SM Vuong, L Hill, C Shula, A Timms, D Beier, K Campbell, ... Development 145 (1), dev154500, 2018 | 67 | 2018 |
| Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence M Lukacs, J Gilley, Y Zhu, G Orsomando, C Angeletti, J Liu, X Yang, ... Experimental neurology 320, 112961, 2019 | 56 | 2019 |
| Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sites SA Jaeger, ET Chan, MF Berger, R Stottmann, TR Hughes, ML Bulyk Genomics 95 (4), 185-195, 2010 | 55 | 2010 |
| Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly A DiStasio, A Driver, K Sund, M Donlin, RM Muraleedharan, S Pooya, ... Human Molecular Genetics 26 (24), 4836-4848, 2017 | 54 | 2017 |
| Cholesterol Metabolism Is Required for Intracellular Hedgehog Signal Transduction In Vivo RW Stottmann, A Turbe-Doan, P Tran, LE Kratz, JL Moran, RI Kelley, ... PLoS genetics 7 (9), e1002224, 2011 | 53 | 2011 |
| Loss of SMPD4 causes a developmental disorder characterized by microcephaly and congenital arthrogryposis P Magini, DJ Smits, L Vandervore, R Schot, M Columbaro, E Kasteleijn, ... The American Journal of Human Genetics 105 (4), 689-705, 2019 | 50 | 2019 |
| Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice Z Li, Y Peng, RB Hufnagel, YC Hu, C Zhao, LF Queme, Z Khuchua, ... Human molecular genetics 26 (19), 3776-3791, 2017 | 49 | 2017 |
| Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse RW Stottmann, JL Moran, A Turbe-Doan, E Driver, M Kelley, DR Beier Genetics 188 (3), 615-624, 2011 | 44 | 2011 |
| Differential requirements of tubulin genes in mammalian forebrain development E Bittermann, Z Abdelhamed, RP Liegel, C Menke, A Timms, DR Beier, ... PLoS genetics 15 (8), e1008243, 2019 | 43 | 2019 |
| ENU Mutagenesis in the Mouse R Stottmann, D Beier Current protocols in human genetics 82 (1), 15.4. 1-15.4. 10, 2014 | 42 | 2014 |
| Distribution of TAG‐1 and synaptophysin in the developing cerebellar cortex: Relationship to Purkinje cell dendritic development RW Stottmann, RJ Rivas Journal of Comparative Neurology 395 (1), 121-135, 1998 | 38 | 1998 |
