Year |
Citation |
Score |
2024 |
Wilderman A, D'haene E, Baetens M, Yankee TN, Winchester EW, Glidden N, Roets E, Van Dorpe J, Janssens S, Miller DE, Galey M, Brown KM, Stottmann RW, Vergult S, Weaver KN, et al. A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature Communications. 15: 136. PMID 38167838 DOI: 10.1038/s41467-023-44506-2 |
0.35 |
|
2023 |
Inskeep KA, Crase B, Stottmann RW. mediated sphingolipid metabolism regulates brain and primary cilia development. Biorxiv : the Preprint Server For Biology. PMID 38168190 DOI: 10.1101/2023.12.15.571873 |
0.81 |
|
2023 |
Smallwood K, Watt KEN, Ide S, Baltrunaite K, Brunswick C, Inskeep K, Capannari C, Adam MP, Begtrup A, Bertola DR, Demmer L, Demo E, Devinsky O, Gallagher ER, Guillen Sacoto MJ, ... ... Stottmann RW, et al. POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies. American Journal of Human Genetics. PMID 37075751 DOI: 10.1016/j.ajhg.2023.03.014 |
0.824 |
|
2023 |
Liegel RP, Michalski MN, Vaidya S, Bittermann E, Finnerty E, Menke CA, Diegel CR, Zhong ZA, Williams BO, Stottmann RW. Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformations. Development (Cambridge, England). 150. PMID 36789910 DOI: 10.1242/dev.201038 |
0.791 |
|
2023 |
Strong A, Rao S, von Hardenberg S, Li D, Cox LL, Lee PC, Zhang LQ, Awotoye W, Diamond T, Gold J, Gooch C, Gowans LJJ, Hakonarson H, Hing A, Loomes K, ... ... Stottmann RW, et al. A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature. American Journal of Medical Genetics. Part A. PMID 36751037 DOI: 10.1002/ajmg.a.63130 |
0.33 |
|
2022 |
Khalaf-Nazzal R, Fasham J, Inskeep KA, Blizzard LE, Leslie JS, Wakeling MN, Ubeyratna N, Mitani T, Griffith JL, Baker W, Al-Hijawi F, Keough KC, Gezdirici A, Pena L, Spaeth CG, ... ... Stottmann RW, et al. Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder. American Journal of Human Genetics. PMID 36283405 DOI: 10.1016/j.ajhg.2022.09.012 |
0.811 |
|
2022 |
Baker EK, Solivio B, Pode-Shakked B, Cross LA, Sullivan B, Raas-Rothschild A, Chorin O, Barel O, Bar-Yosef O, Husami A, Hopkin RJ, Prada CE, Stottmann RW, Weaver KN. PPP2R1A neurodevelopmental disorder is associated with congenital heart defects. American Journal of Medical Genetics. Part A. 188: 3262-3277. PMID 36209351 DOI: 10.1002/ajmg.a.62946 |
0.303 |
|
2021 |
Inskeep KA, Zarate YA, Monteil D, Spranger J, Doherty D, Stottmann RW, Weaver KN. Genetic and phenotypic heterogeneity in KIAA0753-related ciliopathies. American Journal of Medical Genetics. Part A. PMID 34523780 DOI: 10.1002/ajmg.a.62497 |
0.823 |
|
2021 |
Marom R, Burrage LC, Venditti R, Clément A, Blanco-Sánchez B, Jain M, Scott DA, Rosenfeld JA, Sutton VR, Shinawi M, Mirzaa G, DeVile C, Roberts R, Calder AD, Allgrove J, ... ... Stottmann RW, et al. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. American Journal of Human Genetics. PMID 34450031 DOI: 10.1016/j.ajhg.2021.08.002 |
0.324 |
|
2021 |
Blizzard LE, Menke C, Patel SD, Waclaw RR, Lachke SA, Stottmann RW. A Novel Mutation in Cse1l Disrupts Brain and Eye Development with Specific Effects on Pax6 Expression. Journal of Developmental Biology. 9. PMID 34287339 DOI: 10.3390/jdb9030027 |
0.423 |
|
2021 |
Abdelhamed Z, Lukacs M, Cindric S, Ali S, Omran H, Stottmann RW. Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms. 14. PMID 34115122 DOI: 10.1242/dmm.048645 |
0.811 |
|
2021 |
Abdelhamed Z, Lukacs M, Cindric S, Ali S, Omran H, Stottmann RW. Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice Disease Models & Mechanisms. 14: dmm048645. DOI: 10.1242/dmm.048645 |
0.82 |
|
2020 |
Abdelhamed Z, Lukacs M, Cindric S, Omran H, Stottmann RW. A novel hypomorphic allele of causes primary ciliary dyskinesia phenotypes in mice. Disease Models & Mechanisms. PMID 32988999 DOI: 10.1242/Dmm.045344 |
0.837 |
|
2020 |
Lukacs M, Blizzard LE, Stottmann RW. CNS Glycosylphosphatidylinositol Deficiency Results in Delayed White Matter Development, Ataxia, and Premature Death in a Novel Mouse Model. Human Molecular Genetics. PMID 32179897 DOI: 10.1093/Hmg/Ddaa046 |
0.829 |
|
2019 |
DiStasio A, Paulding D, Chaturvedi P, Stottmann RW. Nubp2 is required for cranial neural crest survival in the mouse. Developmental Biology. PMID 31733190 DOI: 10.1016/J.Ydbio.2019.10.039 |
0.791 |
|
2019 |
Snedeker J, Gibbons WJ, Paulding DF, Abdelhamed Z, Prows DR, Stottmann RW. Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants. Plos Genetics. 15: e1008467. PMID 31730647 DOI: 10.1371/Journal.Pgen.1008467 |
0.812 |
|
2019 |
Magini P, Smits DJ, Vandervore L, Schot R, Columbaro M, Kasteleijn E, van der Ent M, Palombo F, Lequin MH, Dremmen M, de Wit MCY, Severino M, Divizia MT, Striano P, Ordonez-Herrera N, ... ... Stottmann RW, et al. Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis. American Journal of Human Genetics. PMID 31495489 DOI: 10.1016/J.Ajhg.2019.08.006 |
0.42 |
|
2019 |
Bittermann E, Abdelhamed Z, Liegel RP, Menke C, Timms A, Beier DR, Stottmann RW. Differential requirements of tubulin genes in mammalian forebrain development. Plos Genetics. 15: e1008243. PMID 31386652 DOI: 10.1371/Journal.Pgen.1008243 |
0.769 |
|
2019 |
Lukacs M, Roberts T, Chatuverdi P, Stottmann RW. Glycosylphosphatidylinositol biosynthesis and remodeling are required for neural tube closure, heart development, and cranial neural crest cell survival. Elife. 8. PMID 31232685 DOI: 10.7554/Elife.45248 |
0.836 |
|
2019 |
Lukacs M, Gilley J, Zhu Y, Orsomando G, Angeletti C, Liu J, Yang X, Park J, Hopkin RJ, Coleman MP, Zhai RG, Stottmann RW. Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence. Experimental Neurology. 112961. PMID 31136762 DOI: 10.1016/J.Expneurol.2019.112961 |
0.805 |
|
2018 |
Liegel RP, Finnerty E, Ward L, DiStasio A, Hufnagel RB, Saal HM, Sund KL, Prows CA, Stottmann R. Using human sequencing to guide craniofacial research. Genesis (New York, N.Y. : 2000). PMID 30375152 DOI: 10.1002/Dvg.23259 |
0.785 |
|
2018 |
Abdelhamed Z, Vuong SM, Hill L, Shula C, Timms A, Beier D, Campbell K, Mangano FT, Stottmann RW, Goto J. A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development (Cambridge, England). 145. PMID 29317443 DOI: 10.1242/Dev.154500 |
0.651 |
|
2017 |
Driver AM, Shumrick C, Stottmann RW. Ttc21b Is Required in Bergmann Glia for Proper Granule Cell Radial Migration. Journal of Developmental Biology. 5. PMID 29615573 DOI: 10.3390/jdb5040018 |
0.656 |
|
2017 |
DiStasio A, Driver A, Sund K, Donlin M, Muraleedharan RM, Pooya S, Kline-Fath B, Kaufman KM, Prows CA, Schorry E, DasGupta B, Stottmann RW. Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly. Human Molecular Genetics. PMID 29036432 DOI: 10.1093/Hmg/Ddx362 |
0.832 |
|
2017 |
Li Z, Peng Y, Hufnagel RB, Hu YC, Zhao C, Queme LF, Khuchua Z, Driver AM, Dong F, Lu QR, Lindquist DM, Jankowski MP, Stottmann RW, Kao WWY, Huang T. Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice. Human Molecular Genetics. 26: 3776-3791. PMID 28934388 DOI: 10.1093/Hmg/Ddx262 |
0.687 |
|
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 |
0.675 |
|
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 |
0.714 |
|
2016 |
Gelineau-Morel R, Lukacs M, Weaver KN, Hufnagel RB, Gilbert DL, Stottmann RW. Congenital Cataracts and Gut Dysmotility in a DYNC1H1 Dyneinopathy Patient. Genes. 7. PMID 27754416 DOI: 10.3390/Genes7100085 |
0.812 |
|
2016 |
Stottmann RW, Driver A, Gutierrez A, Skelton MR, Muntifering M, Stepien C, Knudson L, Kofron M, Vorhees CV, Williams MT. A HETEROZYGOUS MUTATION IN TUBULIN, BETA 2B (TUBB2B) CAUSES COGNITIVE DEFICITS AND HIPPOCAMPAL DISORGANIZATION. Genes, Brain, and Behavior. PMID 27594048 DOI: 10.1111/Gbb.12327 |
0.732 |
|
2016 |
Driver AM, Kratz LE, Kelley RI, Stottmann RW. Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain. Neurobiology of Disease. PMID 26921468 DOI: 10.1016/J.Nbd.2016.02.017 |
0.697 |
|
2015 |
Cionni M, Menke C, Stottmann RW. Novel genetic tools facilitate the study of cortical neuron migration. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 26662625 DOI: 10.1007/S00335-015-9615-6 |
0.435 |
|
2015 |
Jeruschke S, Jeruschke K, DiStasio A, Karaterzi S, Büscher AK, Nalbant P, Klein-Hitpass L, Hoyer PF, Weiss J, Stottmann RW, Weber S. Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 Expression. Plos One. 10: e0137043. PMID 26331477 DOI: 10.1371/Journal.Pone.0137043 |
0.792 |
|
2015 |
Menke C, Cionni M, Siggers T, Bulyk ML, Beier DR, Stottmann RW. Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development. Genesis (New York, N.Y. : 2000). PMID 26177923 DOI: 10.1002/Dvg.22875 |
0.69 |
|
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 |
0.476 |
|
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 |
0.37 |
|
2015 |
Ha S, Stottmann RW, Furley AJ, Beier DR. A forward genetic screen in mice identifies mutants with abnormal cortical patterning. Cerebral Cortex (New York, N.Y. : 1991). 25: 167-79. PMID 23968836 DOI: 10.1093/Cercor/Bht209 |
0.764 |
|
2015 |
Menke C, Cionni M, Siggers T, Bulyk ML, Beier DR, Stottmann RW. Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development Genesis. DOI: 10.1002/dvg.22875 |
0.504 |
|
2014 |
Stottmann R, Beier D. ENU mutagenesis in the mouse Current Protocols in Mouse Biology. 4: 25-35. PMID 25723916 DOI: 10.1002/9780470942390.Mo140029 |
0.637 |
|
2014 |
Cionni M, Menke C, Stottmann RW. The mouse MC13 mutant is a novel ENU mutation in collagen type II, alpha 1. Plos One. 9: e116104. PMID 25541700 DOI: 10.1371/Journal.Pone.0116104 |
0.47 |
|
2014 |
Stottmann R, Beier D. ENU Mutagenesis in the Mouse. Current Protocols in Human Genetics. 82: 15.4.1-10. PMID 25042716 DOI: 10.1002/0471142905.hg1504s82 |
0.598 |
|
2013 |
Stottmann RW, Donlin M, Hafner A, Bernard A, Sinclair DA, Beier DR. A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse. Human Molecular Genetics. 22: 4053-63. PMID 23727838 DOI: 10.1093/Hmg/Ddt255 |
0.71 |
|
2013 |
Tran PV, Lachke SA, Stottmann RW. Toward a systems-level understanding of the Hedgehog signaling pathway: defining the complex, robust, and fragile. Wiley Interdisciplinary Reviews. Systems Biology and Medicine. 5: 83-100. PMID 23060005 DOI: 10.1002/Wsbm.1193 |
0.316 |
|
2012 |
Leshchiner I, Alexa K, Kelsey P, Adzhubei I, Austin-Tse CA, Cooney JD, Anderson H, King MJ, Stottmann RW, Garnaas MK, Ha S, Drummond IA, Paw BH, North TE, Beier DR, et al. Mutation mapping and identification by whole-genome sequencing. Genome Research. 22: 1541-8. PMID 22555591 DOI: 10.1101/Gr.135541.111 |
0.758 |
|
2011 |
Stottmann RW, Turbe-Doan A, Tran P, Kratz LE, Moran JL, Kelley RI, Beier DR. Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo. Plos Genetics. 7: e1002224. PMID 21912524 DOI: 10.1371/Journal.Pgen.1002224 |
0.626 |
|
2011 |
Stottmann RW, Moran JL, Turbe-Doan A, Driver E, Kelley M, Beier DR. Focusing forward genetics: a tripartite ENU screen for neurodevelopmental mutations in the mouse. Genetics. 188: 615-24. PMID 21515572 DOI: 10.1534/Genetics.111.126862 |
0.699 |
|
2011 |
Stottmann RW, Klingensmith J. Bone morphogenetic protein signaling is required in the dorsal neural folds before neurulation for the induction of spinal neural crest cells and dorsal neurons. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 755-65. PMID 21394823 DOI: 10.1002/Dvdy.22579 |
0.356 |
|
2011 |
Stottmann RW, Beier D. ENU mutagenesis identifies novel genes required for forebrain development Developmental Biology. 356: 159. DOI: 10.1016/J.Ydbio.2011.05.589 |
0.627 |
|
2010 |
Stottmann RW, Beier DR. Using ENU mutagenesis for phenotype-driven analysis of the mouse. Methods in Enzymology. 477: 329-48. PMID 20699149 DOI: 10.1016/S0076-6879(10)77017-8 |
0.683 |
|
2010 |
Stottmann RW, Bjork BC, Doyle JB, Beier DR. Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse. Genesis (New York, N.Y. : 2000). 48: 303-8. PMID 20196077 DOI: 10.1002/Dvg.20618 |
0.713 |
|
2010 |
Jaeger SA, Chan ET, Berger MF, Stottmann R, Hughes TR, Bulyk ML. Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sites. Genomics. 95: 185-95. PMID 20079828 DOI: 10.1016/J.Ygeno.2010.01.002 |
0.339 |
|
2009 |
Stottmann RW, Tran PV, Turbe-Doan A, Beier DR. Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain. Developmental Biology. 335: 166-78. PMID 19732765 DOI: 10.1016/J.Ydbio.2009.08.023 |
0.663 |
|
2009 |
Stottmann RW, Turbe-Doan A, Qui H, Beier D. An ENU screen reveals novel genes in mammalian forebrain development Developmental Biology. 331: 495. DOI: 10.1016/J.Ydbio.2009.05.408 |
0.601 |
|
2008 |
Beckstead WA, Bjork BC, Stottmann RW, Sunyaev S, Beier DR. SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 19: 687-90. PMID 18958524 DOI: 10.1007/S00335-008-9149-2 |
0.616 |
|
2008 |
Tran PV, Haycraft CJ, Besschetnova TY, Turbe-Doan A, Stottmann RW, Herron BJ, Chesebro AL, Qiu H, Scherz PJ, Shah JV, Yoder BK, Beier DR. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia. Nature Genetics. 40: 403-10. PMID 18327258 DOI: 10.1038/Ng.105 |
0.65 |
|
2008 |
Stottmann RW, Yun Y, Beier D. An Enu screen reveals novel genes required for mammalian forebrain development Developmental Biology. 319: 599. DOI: 10.1016/J.Ydbio.2008.05.424 |
0.606 |
|
2007 |
Choi M, Stottmann RW, Yang YP, Meyers EN, Klingensmith J. The bone morphogenetic protein antagonist noggin regulates mammalian cardiac morphogenesis. Circulation Research. 100: 220-8. PMID 17218603 DOI: 10.1161/01.Res.0000257780.60484.6A |
0.383 |
|
2007 |
Ackerman KG, Stottmann RW, Yun Y, Luo L, Bolton A, Moran JL, Beier R. Mouse mutagenesis for targeting mutations causing abnormal diaphragm development Developmental Biology. 306: 420-421. DOI: 10.1016/J.Ydbio.2007.03.654 |
0.444 |
|
2007 |
Bolton A, Moran JL, Ackerman KG, Luo L, Beier R, Stottmann RW, Yun Y. WITHDRAWN: Mouse mutagenesis for targeting mutations causing abnormal diaphragm development Developmental Biology. DOI: 10.1016/J.Ydbio.2007.03.308 |
0.444 |
|
2007 |
Stottmann RW, Yun Y, Beier D. An ENU screen for novel genes required in mammalian forebrain development Developmental Biology. 306: 302. DOI: 10.1016/J.Ydbio.2007.03.086 |
0.592 |
|
2006 |
Anderson RM, Stottmann RW, Choi M, Klingensmith J. Endogenous bone morphogenetic protein antagonists regulate mammalian neural crest generation and survival. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 235: 2507-20. PMID 16894609 DOI: 10.1002/Dvdy.20891 |
0.364 |
|
2006 |
Stottmann RW, Berrong M, Matta K, Choi M, Klingensmith J. The BMP antagonist Noggin promotes cranial and spinal neurulation by distinct mechanisms. Developmental Biology. 295: 647-63. PMID 16712836 DOI: 10.1016/J.Ydbio.2006.03.051 |
0.379 |
|
2004 |
Stottmann RW, Choi M, Mishina Y, Meyers EN, Klingensmith J. BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium. Development (Cambridge, England). 131: 2205-18. PMID 15073157 DOI: 10.1242/Dev.01086 |
0.363 |
|
2002 |
Bauer KA, George TM, Enterline DS, Stottmann RW, Melvin EC, Siegel D, Samal S, Hauser MA, Klingensmith J, Nye JS, Speer MC. A novel mutation in the gene encoding noggin is not causative in human neural tube defects. Journal of Neurogenetics. 16: 65-71. PMID 12420790 DOI: 10.1080/Neg.16.1.65.71-1 |
0.523 |
|
2002 |
Anderson RM, Lawrence AR, Stottmann RW, Bachiller D, Klingensmith J. Chordin and noggin promote organizing centers of forebrain development in the mouse. Development (Cambridge, England). 129: 4975-87. PMID 12397106 |
0.319 |
|
2001 |
Stottmann RW, Anderson RM, Klingensmith J. The BMP antagonists Chordin and Noggin have essential but redundant roles in mouse mandibular outgrowth. Developmental Biology. 240: 457-73. PMID 11784076 DOI: 10.1006/Dbio.2001.0479 |
0.452 |
|
Low-probability matches (unlikely to be authored by this person) |
1998 |
Stottmann RW, Rivas RJ. Distribution of TAG-1 and synaptophysin in the developing cerebellar cortex: relationship to Purkinje cell dendritic development. The Journal of Comparative Neurology. 395: 121-35. PMID 9590550 DOI: 10.1002/(Sici)1096-9861(19980525)395:1<121::Aid-Cne9>3.0.Co;2-2 |
0.276 |
|
2023 |
Stottmann RW, Harris MP, Saint-Jeannet JP, Merrill AE, Clouthier DE. The Society for Craniofacial Genetics and Developmental Biology 45th Annual Meeting. American Journal of Medical Genetics. Part A. PMID 37040531 DOI: 10.1002/ajmg.a.63206 |
0.264 |
|
2022 |
Laboy Cintron D, Muir AM, Scott A, McDonald M, Monaghan KG, Santiago-Sim T, Wentzensen IM, De Luca C, Brancati F, Harris DJ, Goueli C, Stottmann R, Prada CE, Biderman Waberski M, et al. A recurrent, pathogenic variant in disrupts actin filament formation and causes microcephaly and speech delay. Hgg Advances. 3: 100072. PMID 35047857 DOI: 10.1016/j.xhgg.2021.100072 |
0.232 |
|
2022 |
Brugmann SA, Merrill AE, Saint-Jeannet JP, Stottmann RW, Clouthier DE. The Society for Craniofacial Genetics and Developmental Biology 44th Annual Meeting. American Journal of Medical Genetics. Part A. PMID 35352468 DOI: 10.1002/ajmg.a.62731 |
0.202 |
|
2020 |
Abell K, Hopkin RJ, Bender PL, Jackson F, Smallwood K, Sullivan B, Stottmann RW, Saal HM, Weaver KN. Mandibulofacial dysostosis with microcephaly: An expansion of the phenotype via parental survey. American Journal of Medical Genetics. Part A. PMID 33247512 DOI: 10.1002/ajmg.a.61977 |
0.192 |
|
2023 |
de Sainte Agathe JM, Pode-Shakked B, Naudion S, Michaud V, Arveiler B, Fergelot P, Delmas J, Keren B, Poirsier C, Alkuraya FS, Tabarki B, Bend E, Davis K, Bebin M, Thompson ML, ... ... Stottmann RW, et al. -related disorder: phenotypic and molecular spectrum. Journal of Medical Genetics. PMID 37185208 DOI: 10.1136/jmg-2022-108803 |
0.176 |
|
2021 |
Weaver KN, Sullivan BR, Balow SA, Hopkin S, Chini BA, Pan BS, Stottmann RW, Bender PL, Hopkin RJ, Zhang X, Saal HM. Robin sequence without cleft palate: Genetic diagnoses and management implications. American Journal of Medical Genetics. Part A. PMID 34569146 DOI: 10.1002/ajmg.a.62515 |
0.159 |
|
2016 |
Go DE, Stottmann RW. The Impact of CRISPR/Cas9-Based Genomic Engineering on Biomedical Research and Medicine. Current Molecular Medicine. 16: 343-52. PMID 26980700 DOI: 10.2174/1566524016666160316150847 |
0.131 |
|
Hide low-probability matches. |