| Year |
Citation |
Score |
| 2019 |
Aldinger KA, Timms AE, Thomson Z, Mirzaa GM, Bennett JT, Rosenberg AB, Roco CM, Hirano M, Abidi F, Haldipur P, Cheng CV, Collins S, Park K, Zeiger J, Overmann LM, et al. Redefining the Etiologic Landscape of Cerebellar Malformations. American Journal of Human Genetics. PMID 31474318 DOI: 10.1016/J.Ajhg.2019.07.019 |
0.31 |
|
| 2018 |
Byers HM, Jensen DM, Glass IA, Bennett JT. Minimal mosaicism, maximal phenotype: Discordance between clinical and molecular findings in two patients with tuberous sclerosis. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 30260069 DOI: 10.1002/Ajmg.C.31656 |
0.3 |
|
| 2018 |
Di Donato N, Timms AE, Aldinger KA, Mirzaa GM, Bennett JT, Collins S, Olds C, Mei D, Chiari S, Carvill G, Myers CT, Rivière JB, Zaki MS, Gleeson JG, et al. Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29671837 DOI: 10.1038/Gim.2018.8 |
0.31 |
|
| 2017 |
Ebrahimi-Fakhari D, Cheng C, Dies K, Diplock A, Pier DB, Ryan CS, Lanpher BC, Hirst J, Chung WK, Sahin M, Rosser E, Darras B, Bennett JT. Clinical and genetic characterization of AP4B1-associated SPG47. American Journal of Medical Genetics. Part A. PMID 29193663 DOI: 10.1002/Ajmg.A.38561 |
0.302 |
|
| 2017 |
Abi Habib W, Brioude F, Edouard T, Bennett JT, Lienhardt-Roussie A, Tixier F, Salem J, Yuen T, Azzi S, Le Bouc Y, Harbison MD, Netchine I. Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28796236 DOI: 10.1038/Gim.2017.105 |
0.343 |
|
| 2016 |
Gripp KW, Aldinger KA, Bennett JT, Baker L, Tusi J, Powell-Hamilton N, Stabley D, Sol-Church K, Timms AE, Dobyns WB. A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair. American Journal of Medical Genetics. Part A. PMID 27264673 DOI: 10.1002/Ajmg.A.37781 |
0.342 |
|
| 2016 |
Bennett JT, Tan TY, Alcantara D, Tétrault M, Timms AE, Jensen D, Collins S, Nowaczyk MJ, Lindhurst MJ, Christensen KM, Braddock SR, Brandling-Bennett H, Hennekam RC, Chung B, Lehman A, et al. Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis. American Journal of Human Genetics. 98: 579-87. PMID 26942290 DOI: 10.1016/J.Ajhg.2016.02.006 |
0.309 |
|
| 2007 |
Bennett JT, Stickney HL, Choi WY, Ciruna B, Talbot WS, Schier AF. Maternal nodal and zebrafish embryogenesis. Nature. 450: E1-2; discussion E2-. PMID 17994032 DOI: 10.1038/Nature06314 |
0.626 |
|
| 2007 |
Bennett JT, Joubin K, Cheng S, Aanstad P, Herwig R, Clark M, Lehrach H, Schier AF. Nodal signaling activates differentiation genes during zebrafish gastrulation. Developmental Biology. 304: 525-40. PMID 17306247 DOI: 10.1016/J.Ydbio.2007.01.012 |
0.642 |
|
| 2003 |
Kunwar PS, Zimmerman S, Bennett JT, Chen Y, Whitman M, Schier AF. Mixer/Bon and FoxH1/Sur have overlapping and divergent roles in Nodal signaling and mesendoderm induction. Development (Cambridge, England). 130: 5589-99. PMID 14522874 DOI: 10.1242/Dev.00803 |
0.604 |
|
| 2003 |
Cheng SK, Olale F, Bennett JT, Brivanlou AH, Schier AF. EGF-CFC proteins are essential coreceptors for the TGF-beta signals Vg1 and GDF1. Genes & Development. 17: 31-6. PMID 12514096 DOI: 10.1101/Gad.1041203 |
0.559 |
|
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