D. M. Juriloff

3.5k total citations
79 papers, 2.8k citations indexed

About

D. M. Juriloff is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, D. M. Juriloff has authored 79 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 40 papers in Genetics and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in D. M. Juriloff's work include Cleft Lip and Palate Research (21 papers), Epigenetics and DNA Methylation (12 papers) and Folate and B Vitamins Research (12 papers). D. M. Juriloff is often cited by papers focused on Cleft Lip and Palate Research (21 papers), Epigenetics and DNA Methylation (12 papers) and Folate and B Vitamins Research (12 papers). D. M. Juriloff collaborates with scholars based in Canada, United States and Germany. D. M. Juriloff's co-authors include Muriel J. Harris, M. J. Harris, Diana Mah, Dixie L. Mager, Liane Gagnier, Carolyn J. Brown, Teresa M. Gunn, F. Clarke Fraser, Andrew C. Lidral and Thomas J. Carroll and has published in prestigious journals such as Development, Journal of Virology and Human Molecular Genetics.

In The Last Decade

D. M. Juriloff

77 papers receiving 2.7k citations

Peers

D. M. Juriloff

GENET

PPCH

RHEUM

SURGE

Frances A. Brook United Kingdom

Andreas Winterpacht Germany

Zoha Kibar Canada

Elisa Merello Italy

F. Dagna Bricarelli Italy

E. Niebuhr Denmark

Oliver Bartsch Germany

Dieter Kotzot Austria

Dvorah Abeliovich Israel

Peter Wieacker Germany

Frances A. Brook United Kingdom

D. M. Juriloff

2.8k ×1.8

524 ×0.5

GENET

248 ×0.3

PPCH

196 ×0.3

RHEUM

501 ×1.1

SURGE

Citations per year, relative to D. M. Juriloff D. M. Juriloff (= 1×) peers Frances A. Brook

Countries citing papers authored by D. M. Juriloff

Since Specialization

Citations

This map shows the geographic impact of D. M. Juriloff's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by D. M. Juriloff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. M. Juriloff more than expected).

Fields of papers citing papers by D. M. Juriloff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. M. Juriloff. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by D. M. Juriloff. The network helps show where D. M. Juriloff may publish in the future.

Co-authorship network of co-authors of D. M. Juriloff

This figure shows the co-authorship network connecting the top 25 collaborators of D. M. Juriloff. A scholar is included among the top collaborators of D. M. Juriloff based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with D. M. Juriloff. D. M. Juriloff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Juriloff, D. M. & Muriel J. Harris. (2012). A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects. Birth Defects Research Part A Clinical and Molecular Teratology. 94(10). 824–840. 112 indexed citations

Harris, Muriel J. & D. M. Juriloff. (2010). An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. Birth Defects Research Part A Clinical and Molecular Teratology. 88(8). 653–669. 248 indexed citations

Juriloff, D. M. & Muriel J. Harris. (2008). Mouse genetic models of cleft lip with or without cleft palate. Birth Defects Research Part A Clinical and Molecular Teratology. 82(2). 63–77. 110 indexed citations

Juriloff, D. M., Muriel J. Harris, Andrew P. McMahon, Thomas J. Carroll, & Andrew C. Lidral. (2006). Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Birth Defects Research Part A Clinical and Molecular Teratology. 76(8). 574–579. 105 indexed citations

Harris, Muriel J. & D. M. Juriloff. (2006). Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Research Part A Clinical and Molecular Teratology. 79(3). 187–210. 245 indexed citations

Juriloff, D. M., Muriel J. Harris, Carolyn J. Brown, et al.. (2005). Investigations of the genomic region that contains the clf1 mutation, a causal gene in multifactorial cleft lip and palate in mice. Birth Defects Research Part A Clinical and Molecular Teratology. 73(2). 103–113. 53 indexed citations

Juriloff, D. M., Muriel J. Harris, & Diana Mah. (2004). The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene. Genomics. 85(1). 139–142. 10 indexed citations

Juriloff, D. M., et al.. (2004). A digenic cause of cleft lip in A‐strain mice and definition of candidate genes for the two loci. Birth Defects Research Part A Clinical and Molecular Teratology. 70(8). 509–518. 31 indexed citations

Juriloff, D. M., Muriel J. Harris, & Carolyn J. Brown. (2001). Unravelling the complex genetics of cleft lip in the mouse model. Mammalian Genome. 12(6). 426–435. 48 indexed citations

10.

Juriloff, D. M., Muriel J. Harris, Kathleen G. Banks, & Diana Mah. (2000). Gaping lids, gp, a mutation on centromeric Chromosome 11 that causes defective eyelid development in mice. Mammalian Genome. 11(6). 440–447. 9 indexed citations

11.

Hofmann, Michael W., Muriel J. Harris, D. M. Juriloff, & Thomas Boehm. (1998). Spontaneous Mutations in SELH/Bc Mice Due to Insertions of Early Transposons: Molecular Characterization of Null Alleles at thenudeandalbinoLoci. Genomics. 52(1). 107–109. 30 indexed citations

12.

Harris, M. J. & D. M. Juriloff. (1998). Nonallelic noncomplementation models in mice: The first arch and lidgap-Gates mutations. Genome. 41(6). 789–796. 7 indexed citations

13.

Harris, M. J. & D. M. Juriloff. (1997). Genetic landmarks for defects in mouse neural tube closure. Teratology. 56(3). 177–187. 50 indexed citations

14.

Juriloff, D. M., M. J. Harris, & Diana Mah. (1996). The clf1 gene maps to a 2- to 3-cM region of distal mouse Chromosome 11. Mammalian Genome. 7(10). 789–789. 11 indexed citations

15.

Juriloff, D. M., Susan D. Porter, & M. J. Harris. (1994). Three spontaneous mutations at the albino locus in SELH/Bc mice. Genome. 37(2). 190–197. 8 indexed citations

16.

Juriloff, D. M., M. J. Harris, & Diana Mah. (1994). Mapping Far (First arch) in relation to molecular markers on mouse Chromosome 2. Mammalian Genome. 5(7). 450–452. 4 indexed citations

17.

Harris, M. J., D. M. Juriloff, Teresa M. Gunn, & Jason E. Miller. (1994). Development of the cerebellar defect in ataxic SELH/Bc mice. Teratology. 50(1). 63–73. 12 indexed citations

18.

Juriloff, D. M., et al.. (1991). Studies of the effect of retinoic acid on anterior neural tube closure in mice genetically liable to exencephaly. Teratology. 43(1). 27–40. 39 indexed citations

19.

Juriloff, D. M., et al.. (1989). Genetic analysis of the cause of exencephaly in the SELH/Bc mouse stock. Teratology. 40(4). 395–405. 37 indexed citations

20.

Juriloff, D. M., et al.. (1980). Morphogenesis of spontaneously occurring otocephaly in a newly developed mouse mutant. Birth Defects Research. 21(2). 47–48. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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