F. J. Dill

1.3k total citations
24 papers, 897 citations indexed

About

F. J. Dill is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, F. J. Dill has authored 24 papers receiving a total of 897 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in F. J. Dill's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). F. J. Dill is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). F. J. Dill collaborates with scholars based in Canada, United States and Tunisia. F. J. Dill's co-authors include DK Kalousek, Dagmar K. Kalousek, Barbara McGillivray, Betty J. Poland, Siu Li Yong, Tapio Pantzar, R. Douglas Wilson, Diana S. Herbst, Stephen Wood and Jim Miller and has published in prestigious journals such as Nature, Science and The Journal of Pediatrics.

In The Last Decade

F. J. Dill

24 papers receiving 807 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
F. J. Dill	579	486	242	132	112	24	897
Iris Bartels	643 1.1×	738 1.5×	305 1.3×	159 1.2×	130 1.2×	69	1.3k
Thue Bryndorf	516 0.9×	445 0.9×	272 1.1×	185 1.4×	87 0.8×	29	997
G. Lefort	377 0.7×	290 0.6×	189 0.8×	74 0.6×	58 0.5×	34	632
Isabel Lorda‐Sánchez	759 1.3×	689 1.4×	558 2.3×	82 0.6×	130 1.2×	67	1.4k
M. Ray	731 1.3×	377 0.8×	391 1.6×	65 0.5×	73 0.7×	36	1.1k
Constantinos Pángalos	337 0.6×	297 0.6×	220 0.9×	88 0.7×	41 0.4×	38	643
G. L. Terzoli	397 0.7×	517 1.1×	237 1.0×	84 0.6×	146 1.3×	14	843
Janice Matsuura	585 1.0×	855 1.8×	181 0.7×	564 4.3×	94 0.8×	11	1.2k
Walter Fuhrmann	424 0.7×	261 0.5×	259 1.1×	56 0.4×	160 1.4×	86	898
Kenneth L. Garver	260 0.4×	225 0.5×	160 0.7×	88 0.7×	187 1.7×	24	712

Countries citing papers authored by F. J. Dill

Since Specialization

Citations

This map shows the geographic impact of F. J. Dill'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 F. J. Dill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. J. Dill more than expected).

Fields of papers citing papers by F. J. Dill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. J. Dill. 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 F. J. Dill. The network helps show where F. J. Dill may publish in the future.

Co-authorship network of co-authors of F. J. Dill

This figure shows the co-authorship network connecting the top 25 collaborators of F. J. Dill. A scholar is included among the top collaborators of F. J. Dill 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 F. J. Dill. F. J. Dill is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Vincent, John B., Sanaa Choufani, Shin‐ichi Horike, et al.. (2008). A translocation t(6;7)(p11–p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints. Psychiatric Genetics. 18(3). 101–109. 11 indexed citations

Dill, F. J., et al.. (2001). Grandmaternal origin of an isochromosome 18p present in two maternal half-sisters. American Journal of Medical Genetics. 101(1). 65–69. 40 indexed citations

Lopez‐Rangel, Elena, F. J. Dill, Monica Hrynchak, & M. I. Van Allen. (1993). Partial duplication of 3q (q25.1→q26.1) without the Brachmann‐de Lange phenotype. American Journal of Medical Genetics. 47(7). 1068–1071. 15 indexed citations

Miller, Diane, F. J. Dill, Jay B. Lichter, Kenneth K. Kídd, & Paul J. Goodfellow. (1992). Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. Genomics. 13(3). 601–606. 10 indexed citations

Dill, F. J., et al.. (1987). X chromosome aneuploidy in lymphocyte cultures from women with recurrent spontaneous abortions. American Journal of Medical Genetics. 28(4). 981–987. 39 indexed citations

Dill, F. J., et al.. (1987). Inverted tandem duplication generates a duplication deficiency of chromosome 8p. Clinical Genetics. 32(2). 109–113. 38 indexed citations

Kalousek, Dagmar K., F. J. Dill, Tapio Pantzar, et al.. (1987). Confined chorionic mosaicism in prenatal diagnosis. Human Genetics. 77(2). 163–167. 115 indexed citations

Horsman, Douglas E., J. Tapio Pantzar, F. J. Dill, & Dagmar K. Kalousek. (1987). Klinefelter's syndrome and acute leukemia. Cancer Genetics and Cytogenetics. 26(2). 375–376. 27 indexed citations

Froster‐Iskenius, U., F. J. Dill, Judith G. Hall, et al.. (1986). Normal male carriers in the fra(X) form of X‐linked mental retardation (Martin—Bell syndrome). American Journal of Medical Genetics. 23(1-2). 619–631. 21 indexed citations

10.

Jacky, Peter B. & F. J. Dill. (1983). Fragile X chromosome and chromosome condensation.. PubMed. 26(3). 171–3. 3 indexed citations

11.

Kalousek, DK & F. J. Dill. (1983). Chromosomal Mosaicism Confined to the Placenta in Human Conceptions. Science. 221(4611). 665–667. 277 indexed citations

12.

Harris, M. J., Betty J. Poland, & F. J. Dill. (1981). Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos.. PubMed. 57(5). 600–6. 22 indexed citations

13.

Herbst, Diana S., et al.. (1981). Further delineation of X-linked mental retardation. Human Genetics. 58(4). 366–372. 48 indexed citations

14.

Poland, Betty J., et al.. (1980). A turner‐like phenotype in the aborted fetus. Teratology. 21(3). 361–365. 18 indexed citations

15.

Dill, F. J., et al.. (1980). Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation. Human Genetics. 53(2). 267–9. 47 indexed citations

16.

Poland, Betty J., et al.. (1977). EMBRYONIC DEVELOPMENT IN ECTOPIC HUMAN PREGNANCY. Obstetrical & Gynecological Survey. 32(5). 304–305. 3 indexed citations

17.

Martin, Renée H., F. J. Dill, & Jim Miller. (1976). Nondisjunction in aging female mice. Cytogenetic and Genome Research. 17(3). 150–160. 36 indexed citations

18.

Dill, F. J., et al.. (1973). THE CHROMOSOME COMPLEMENT OF THE NARWHAL (Monodon monoceros). Canadian Journal of Genetics and Cytology. 15(2). 349–353. 6 indexed citations

19.

Miller, James R., et al.. (1970). A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome.. Journal of Medical Genetics. 7(4). 389–393. 11 indexed citations

20.

Robinson, Geoffrey C., et al.. (1964). Klinefelter's syndrome with the XXYY sex chromosome complex. The Journal of Pediatrics. 65(2). 226–232. 28 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.

Explore authors with similar magnitude of impact