| # | Title | Journal | Year | Citations |
|---|
| 1 | Telomerase activity in human germline and embryonic tissues and cells | Genesis | 1996 | 1,172 |
| 2 | Ventral mesodermal patterning inXenopus embryos: Expression patterns and activities of BMP-2 and BMP-4 | Genesis | 1995 | 320 |
| 3 | Mice lackingBmp6 function | Genesis | 1998 | 319 |
| 4 | DNA methylation in plants | Genesis | 1987 | 250 |
| 5 | Epigenetics: An overview | Genesis | 1994 | 208 |
| 6 | Expression of green fluorescent protein in the ureteric bud of transgenic mice: A new tool for the analysis of ureteric bud morphogenesis | Genesis | 1999 | 208 |
| 7 | Fusome asymmetry and oocyte determination inDrosophila | Genesis | 1995 | 203 |
| 8 | Responsiveness of developing dental tissues to fibroblast growth factors: expression of splicing alternatives of FGFR1, -2, -3, and of FGFR4; and stimulation of cell proliferation by FGF-2, -4, -8, and -9 | Genesis | 1998 | 187 |
| 9 | Specific protection from phenocopy induction by heat shock | Genesis | 1979 | 183 |
| 10 | Cellular morphogenesis in theSaccharomyces cerevisiae cell cycle: Localization of theCDC11 gene product and the timing of events at the budding site | Genesis | 1991 | 182 |
| 11 | Genetic control of morphogenesis inArabidopsis | Genesis | 1988 | 179 |
| 12 | Connexin45 (?6) expression delineates an extended conduction system in the embryonic and mature rodent heart | Genesis | 1999 | 178 |
| 13 | Heart development inDrosophila and vertebrates: Conservation of molecular mechanisms | Genesis | 1998 | 171 |
| 14 | Temperature-dependent sex determination in reptiles: Proximate mechanisms, ultimate outcomes, and practical applications | Genesis | 1994 | 169 |
| 15 | There are two mechanisms of achiasmate segregation inDrosophila females, one of which requires heterochromatic homology | Genesis | 1992 | 167 |
| 16 | Screening mosaic F1 females for mutations affecting zebrafish heart induction and patterning | Genesis | 1998 | 162 |
| 17 | Xenopus Pax-2/5/8 orthologues: Novel insights intoPaxGene evolution and identification of Pax-8 as the earliest marker for otic and pronephric cell lineages | Genesis | 1999 | 149 |
| 18 | Is the sphere organelle/coiled body a universal nuclear component? | Genesis | 1995 | 147 |
| 19 | Genetics of sex determination in flowering plants | Genesis | 1994 | 142 |
| 20 | Regionalisation of cell fate and morphogenetic movement of the mesoderm during mouse gastrulation | Genesis | 1995 | 142 |
| 21 | Heat shock induced proteins in plant cells | Genesis | 1979 | 141 |
| 22 | Tissue-specific expression of heat shock proteins of the mouse in the absence of stress | Genesis | 1993 | 141 |
| 23 | Control of in vitro growth of viviparous embryo mutants of maize by abscisic acid | Genesis | 1979 | 137 |
| 24 | Elevated paraquat resistance can be used as a bioassay for longevity in a genetically based long-lived strain ofDrosophila | Genesis | 1991 | 137 |
| 25 | Polarization of mitochondria in the unfertilized mouse oocyte | Genesis | 1995 | 130 |
| 26 | Suppression of human prostate cancer cell growth by forced expression of connexin genes | Genesis | 1999 | 130 |
| 27 | Epigenetic programming of differential gene expression in development and evolution | Genesis | 1995 | 128 |
| 28 | Embryonic expression of the singleTribolium engrailed homolog | Genesis | 1994 | 126 |
| 29 | Developmental expression of urine concentration-associated genes and their altered expression in murine infantile-type polycystic kidney disease | Genesis | 1999 | 125 |
| 30 | Cloning and sequence comparison of the mouse, human, and chickenengrailed genes reveal potential functional domains and regulatory regions | Genesis | 1992 | 124 |
| 31 | The making of a spermatozoon: A molecular perspective | Genesis | 1995 | 121 |
| 32 | Genetic aspects of embryonic eye development in vertebrates | Genesis | 1996 | 121 |
| 33 | Development and tissue-specific distribution of mouse small heat shock protein hsp25 | Genesis | 1993 | 118 |
| 34 | Diverse programs of ascus development in pseudohomothallic species ofNeurospora,Gelasinospora, andPodospora | Genesis | 1994 | 115 |
| 35 | Behavioral and neurobiological implications of sex-determining factors inDrosophila | Genesis | 1994 | 115 |
| 36 | Screen for mutations affecting development of zebrafish neural crest | Genesis | 1996 | 114 |
| 37 | Rapid induction and clearance of TGFβ1 is an early response to wounding in the mouse embryo | Genesis | 1993 | 113 |
| 38 | Skeletal abnormalities in doubly heterozygousBmp4 andBmp7 mice | Genesis | 1998 | 113 |
| 39 | Activation of the cardiac α-actin promoter depends upon serum response factor,Tinman homologue, Nkx-2.5, and intact serum response elements | Genesis | 1996 | 112 |
| 40 | Mutations affecting embryonic cell migrations inCaenorhabditis elegans | Genesis | 1990 | 110 |
| 41 | Homeotic gene expression in the locustSchistocerca: An antibody that detects conserved epitopes in ultrabithorax and abdominal-A proteins | Genesis | 1994 | 107 |
| 42 | Advantages of sexual reproduction | Genesis | 1994 | 107 |
| 43 | Localization of proteins to the apico-lateral junctions ofDrosophila epithelia | Genesis | 1997 | 106 |
| 44 | Mutations affecting eye morphology in the developing zebrafish (Danio rerio) | Genesis | 1997 | 105 |
| 45 | Effect of mutations in thePINHEAD gene ofArabidopsis on the formation of shoot apical meristems | Genesis | 1995 | 104 |
| 46 | MADS-box genes active in developing pollen cones of Norway spruce (Picea abies) are homologous to the B-class floral homeotic genes in angiosperms | Genesis | 1999 | 103 |
| 47 | Use of a tomato mutant constructed with reverse genetics to study fruit ripening, a complex developmental process | Genesis | 1993 | 100 |
| 48 | Podocyte differentiation in the absence of endothelial cells as revealed in the zebrafish avascular mutant,cloche | Genesis | 1999 | 99 |
| 49 | Generating lineage-specific markers to studyDrosophila development | Genesis | 1991 | 98 |
| 50 | Towards an understanding of position effect variegation | Genesis | 1989 | 93 |
