Julie Leana‐Cox

569 total citations
14 papers, 412 citations indexed

About

Julie Leana‐Cox is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Julie Leana‐Cox has authored 14 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Julie Leana‐Cox's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers) and Congenital heart defects research (4 papers). Julie Leana‐Cox is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (5 papers) and Congenital heart defects research (4 papers). Julie Leana‐Cox collaborates with scholars based in United States and Italy. Julie Leana‐Cox's co-authors include Stuart Schwartz, Lauren S. Jenkins, Eric A. Wulfsberg, Beth A. Sullivan, Amy E. Wandstrat, Joleen L. Zackowski, Giovanni Neri, Evelyn M. Karson, Wendy L. Flejter and Rina Plattner and has published in prestigious journals such as The American Journal of Human Genetics, Genomics and American Journal of Medical Genetics.

In The Last Decade

Julie Leana‐Cox

14 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Julie Leana‐Cox United States	9	334	216	139	101	49	14	412
Sigrid Sahlén Sweden	11	327 1.0×	243 1.1×	148 1.1×	115 1.1×	16 0.3×	21	466
D A Couzin United Kingdom	12	226 0.7×	135 0.6×	117 0.8×	124 1.2×	17 0.3×	23	367
Gordon S. Stephen United Kingdom	8	171 0.5×	100 0.5×	62 0.4×	66 0.7×	16 0.3×	15	239
Drew Duckett United Kingdom	9	249 0.7×	142 0.7×	63 0.5×	128 1.3×	12 0.2×	23	353
Fernando Santos Spain	9	228 0.7×	193 0.9×	21 0.2×	84 0.8×	30 0.6×	13	325
Franca Bernardi Italy	10	246 0.7×	116 0.5×	128 0.9×	93 0.9×	8 0.2×	13	367
N. Morichon-Delvallez France	12	320 1.0×	173 0.8×	74 0.5×	143 1.4×	8 0.2×	26	418
Carole Goumy France	11	185 0.6×	125 0.6×	51 0.4×	100 1.0×	17 0.3×	36	324
Patrick L. Wilmot United States	10	148 0.4×	95 0.4×	29 0.2×	49 0.5×	18 0.4×	26	238
Barbara Delle Chiaie Belgium	7	251 0.8×	195 0.9×	38 0.3×	136 1.3×	48 1.0×	10	423

Countries citing papers authored by Julie Leana‐Cox

Since Specialization

Citations

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

Fields of papers citing papers by Julie Leana‐Cox

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julie Leana‐Cox. 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 Julie Leana‐Cox. The network helps show where Julie Leana‐Cox may publish in the future.

Co-authorship network of co-authors of Julie Leana‐Cox

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

All Works

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14 of 14 papers shown

1.

Wandstrat, Amy E., Julie Leana‐Cox, Lauren S. Jenkins, & Stuart Schwartz. (1998). Molecular Cytogenetic Evidence for a Common Breakpoint in the Largest Inverted Duplications of Chromosome 15. The American Journal of Human Genetics. 62(4). 925–936. 64 indexed citations

2.

Schwartz, Stuart, Theresa W. Depinet, Julie Leana‐Cox, et al.. (1997). Sex chromosome markers: Characterization using fluorescence in situ hybridization and review of the literature. American Journal of Medical Genetics. 71(1). 1–7. 27 indexed citations

3.

McDaniel, Lisa D., et al.. (1997). Construction and Screening of a Cosmid Library Generated from a Somatic Cell Hybrid Bearing Human Chromosome 15. Genomics. 40(1). 63–72. 1 indexed citations

4.

Wulfsberg, Eric A., Julie Leana‐Cox, & Giovanni Neri. (1997). Reply to “What's in a name? The 22q11.2 deletion”. American Journal of Medical Genetics. 72(2). 248–249. 2 indexed citations

5.

Leana‐Cox, Julie, et al.. (1996). Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area22q11.2: Report of five families with a review of the literature. American Journal of Medical Genetics. 65(4). 309–316. 62 indexed citations

6.

Sullivan, Beth A., Lauren S. Jenkins, Evelyn M. Karson, Julie Leana‐Cox, & Stuart Schwartz. (1996). Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.. PubMed. 59(1). 167–75. 51 indexed citations

7.

Wulfsberg, Eric A., Julie Leana‐Cox, & Giovanni Neri. (1996). What's in a name? chromosome 22q abnormalities and the DiGeorge, velocardiofacial, and conotruncal anomalies face syndromes. American Journal of Medical Genetics. 65(4). 317–319. 38 indexed citations

8.

Leana‐Cox, Julie, et al.. (1996). Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area22q11.2: Report of five families with a review of the literature. American Journal of Medical Genetics. 65(4). 309–316. 5 indexed citations

9.

Sullivan, Beth A., et al.. (1995). Application of FISH to complex chromosomal rearrangements associated with chronic myelogenous leukemia. Cancer Genetics and Cytogenetics. 82(2). 93–99. 7 indexed citations

10.

Leana‐Cox, Julie, Lauren S. Jenkins, Catherine G. Palmer, et al.. (1994). Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.. PubMed. 54(5). 748–56. 97 indexed citations

11.

Schwartz, Stuart & Julie Leana‐Cox. (1993). Fluorescent in situ hybridization (FISH): A new application in the delineation of true vs. pseudomosaicism in prenatal diagnosis. Prenatal Diagnosis. 13(8). 661–670. 5 indexed citations

12.

Rosenblum‐Vos, Lynne S., Stephen J. Meltzer, Julie Leana‐Cox, & Stuart Schwartz. (1993). Cytogenetic studies of primary cultures of esophageal squamous cell carcinoma. Cancer Genetics and Cytogenetics. 70(2). 127–131. 13 indexed citations

13.

Leana‐Cox, Julie, Sondra W. Levin, Eric A. Wulfsberg, et al.. (1993). Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries.. Europe PMC (PubMed Central). 52(6). 1067–73. 25 indexed citations

14.

Sullivan, Beth A., Julie Leana‐Cox, & Stuart Schwartz. (1993). Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization. American Journal of Medical Genetics. 47(2). 223–230. 15 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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