Wayne H. Finley

720 total citations
39 papers, 561 citations indexed

About

Wayne H. Finley is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wayne H. Finley has authored 39 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 16 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wayne H. Finley's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Wayne H. Finley is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Wayne H. Finley collaborates with scholars based in United States, France and Netherlands. Wayne H. Finley's co-authors include Sara Finley, Andrew J. Carroll, Zhou Zhu, K. H. Gustavson, Gretchen Wells, Bengt Hagberg, John Longshore, Edward V. Colvin, John A. Monti and John M. Opitz and has published in prestigious journals such as Nature, New England Journal of Medicine and JAMA.

In The Last Decade

Wayne H. Finley

38 papers receiving 515 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Wayne H. Finley United States	15	225	199	130	72	56	39	561
R. Dwain Blackston United States	11	232 1.0×	279 1.4×	303 2.3×	62 0.9×	107 1.9×	16	741
Alida C. Knegt Netherlands	14	271 1.2×	257 1.3×	232 1.8×	71 1.0×	120 2.1×	35	652
Job Jc France	9	127 0.6×	132 0.7×	75 0.6×	37 0.5×	25 0.4×	109	356
Roberto Quadrelli United States	10	345 1.5×	186 0.9×	72 0.6×	82 1.1×	16 0.3×	26	602
Gabriel S. Khodr United States	17	173 0.8×	330 1.7×	383 2.9×	76 1.1×	270 4.8×	29	1.1k
Osman Demırhan Türkiye	14	222 1.0×	235 1.2×	139 1.1×	59 0.8×	138 2.5×	72	662
E. Robert Wassman United States	13	223 1.0×	375 1.9×	136 1.0×	83 1.2×	31 0.6×	23	603
L. Bassas Spain	18	361 1.6×	272 1.4×	86 0.7×	120 1.7×	114 2.0×	29	807
Susan H. Black United States	20	275 1.2×	505 2.5×	632 4.9×	166 2.3×	146 2.6×	41	1.2k
Theodore F. Thurmon United States	12	111 0.5×	122 0.6×	39 0.3×	25 0.3×	14 0.3×	29	393

Countries citing papers authored by Wayne H. Finley

Since Specialization

Citations

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

Fields of papers citing papers by Wayne H. Finley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wayne H. Finley. 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 Wayne H. Finley. The network helps show where Wayne H. Finley may publish in the future.

Co-authorship network of co-authors of Wayne H. Finley

This figure shows the co-authorship network connecting the top 25 collaborators of Wayne H. Finley. A scholar is included among the top collaborators of Wayne H. Finley 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 Wayne H. Finley. Wayne H. Finley 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

Drenth, Joost P.H., Wayne H. Finley, Guido J. Breedveld, et al.. (2001). The Primary Erythermalgia–Susceptibility Gene Is Located on Chromosome 2q31-32. The American Journal of Human Genetics. 68(5). 1277–1282. 57 indexed citations

Descartes, Maria, Kim M. Keppler‐Noreuil, Judith Knops, et al.. (1996). Terminal deletion of the long arm of chromosome 4 in a mother and two sons. Clinical Genetics. 50(6). 538–540. 26 indexed citations

Han, Jian, et al.. (1994). Over-representation of the disease associated (CAG) and (CGG) repeats in the human genome. Nucleic Acids Research. 22(9). 1735–1740. 29 indexed citations

George, Alfred L., et al.. (1994). Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23. Genomics. 19(2). 395–397. 9 indexed citations

Finley, Wayne H., et al.. (1994). Birth Defects Surveillance: Jefferson County, Alabama, and Uppsala County, Sweden. Southern Medical Journal. 87(4). 440–445. 22 indexed citations

Weekes, Elizabeth, et al.. (1994). Relationship between amniotic fluid and maternal blood nutrient levels. Journal of Perinatal Medicine. 22(3). 227–234. 12 indexed citations

Han, Jian, et al.. (1994). Selection of Antisense Oligonucleotides on the Basis of Genomic Frequency of the Target Sequence. PubMed. 4(1). 53–65. 21 indexed citations

Wells, Gretchen, et al.. (1994). Congenital Heart Disease in Infants With Downʼs Syndrome. Southern Medical Journal. 87(7). 724–727. 49 indexed citations

Lubs, Herbert A., Louis J. Elsas, Avirachan T. Tharapel, et al.. (1993). Position statement on interphase in situ hybridization prenatal diagnosis. American Journal of Medical Genetics. 46(4). 478–478. 4 indexed citations

10.

Takaesu, Norma T., et al.. (1992). Molecular and cytogenetic investigation of complex tissue‐specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype. American Journal of Medical Genetics. 43(3). 554–560. 7 indexed citations

11.

Finley, Wayne H., Alston Callahan, & Jerry N. Thompson. (1990). Parental age in the blepharophimosis, ptosis, epicanthus inversus, telecanthus complex. American Journal of Medical Genetics. 36(4). 414–417. 5 indexed citations

12.

Carroll, Andrew J., et al.. (1988). Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence. Prenatal Diagnosis. 8(3). 169–174. 15 indexed citations

13.

Finley, Wayne H.. (1981). Ring 4 Chromosome With Terminal p and q Deletions. Archives of Pediatrics and Adolescent Medicine. 135(8). 729–729. 8 indexed citations

14.

Finley, Wayne H.. (1978). Delivering Genetic Services. Pediatric Annals. 7(6). 13–16.

15.

Finley, Wayne H., et al.. (1973). Clinical Features Associated with the Chromosomal Deletion Syndrome Manifested by an 18 Ring (46,18r). Southern Medical Journal. 66(6). 658–660. 4 indexed citations

16.

Finley, Wayne H., et al.. (1972). Triploidy in a live-born male infant. The Journal of Pediatrics. 81(4). 855–856. 11 indexed citations

17.

Finley, Sara, et al.. (1969). Cataracts in a girl with features of the Smith-Lemli-Opitz syndrome. The Journal of Pediatrics. 75(4). 706–707. 25 indexed citations

18.

Finley, Wayne H., et al.. (1968). Four Stem-Line Mosaicism (XO/XY/XXY/XYY) in an Infant with Ambiguous External Genitalia. The Journal of Clinical Endocrinology & Metabolism. 28(2). 239–243. 3 indexed citations

19.

Finley, Wayne H., et al.. (1964). The bone-marrow depressant and antitumor properties in animals of some new alkylating agents. Cancer. 17(10). 1271–1278. 4 indexed citations

20.

Gustavson, K. H., Bengt Hagberg, Sara Finley, & Wayne H. Finley. (1962). An Apparently Identical Extra Autosome in two Severely Retarded Sisters with Multiple Malformations. Cytogenetic and Genome Research. 1(1). 32–41. 38 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