LuAnn Judis

618 total citations
7 papers, 458 citations indexed

About

LuAnn Judis is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, LuAnn Judis has authored 7 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in LuAnn Judis's work include Prenatal Screening and Diagnostics (5 papers), DNA Repair Mechanisms (4 papers) and Genomic variations and chromosomal abnormalities (2 papers). LuAnn Judis is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), DNA Repair Mechanisms (4 papers) and Genomic variations and chromosomal abnormalities (2 papers). LuAnn Judis collaborates with scholars based in United States and United Kingdom. LuAnn Judis's co-authors include E. Ricky Chan, Terry Hassold, Stuart Schwartz, Allen D. Seftel, Audrey Lynn, Patricia A. Hunt, Kara E. Koehler, Patricia A. Jacobs, A D Seftel and Anthony J. Thomas and has published in prestigious journals such as Science, The American Journal of Human Genetics and Fertility and Sterility.

In The Last Decade

LuAnn Judis

7 papers receiving 447 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
LuAnn Judis United States	7	310	180	162	129	55	7	458
Geneviève Lefort France	13	148 0.5×	262 1.5×	105 0.6×	160 1.2×	34 0.6×	29	375
Mary-Ann Mastrangelo United States	10	537 1.7×	214 1.2×	66 0.4×	54 0.4×	61 1.1×	10	622
Anna Frackiewicz United Kingdom	9	200 0.6×	390 2.2×	209 1.3×	185 1.4×	71 1.3×	9	532
Roberto Coco Argentina	12	213 0.7×	401 2.2×	143 0.9×	156 1.2×	63 1.1×	45	531
P.J. Turek United States	14	273 0.9×	181 1.0×	93 0.6×	79 0.6×	198 3.6×	18	579
Takayuki Hirota United Kingdom	9	510 1.6×	201 1.1×	59 0.4×	86 0.7×	111 2.0×	9	588
Kenji Funaki Japan	9	176 0.6×	105 0.6×	124 0.8×	58 0.4×	94 1.7×	16	355
O. Gabriel-Robez France	16	252 0.8×	466 2.6×	332 2.0×	133 1.0×	52 0.9×	29	610
Capucine Hyon France	12	210 0.7×	262 1.5×	47 0.3×	98 0.8×	64 1.2×	21	376
A. P. Dyban Russia	11	245 0.8×	173 1.0×	80 0.5×	104 0.8×	153 2.8×	42	417

Countries citing papers authored by LuAnn Judis

Since Specialization

Citations

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

Fields of papers citing papers by LuAnn Judis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by LuAnn Judis. 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 LuAnn Judis. The network helps show where LuAnn Judis may publish in the future.

Co-authorship network of co-authors of LuAnn Judis

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

All Works

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7 of 7 papers shown

1.

Mitchell, Anna L., et al.. (2011). Characterization of Tissue-Specific and Developmentally Regulated Alternative Splicing of Exon 64 in theCOL5A1Gene. Connective Tissue Research. 53(3). 267–276. 7 indexed citations

2.

Chan, E. Ricky, Andrew Collins, LuAnn Judis, et al.. (2007). The origin of trisomy 13. American Journal of Medical Genetics Part A. 143A(19). 2242–2248. 23 indexed citations

3.

Judis, LuAnn, E. Ricky Chan, Stuart Schwartz, et al.. (2005). Meiotic Synapsis Proceeds from a Limited Number of Subtelomeric Sites in the Human Male. The American Journal of Human Genetics. 77(4). 556–566. 53 indexed citations

4.

Judis, LuAnn, E. Ricky Chan, Stuart Schwartz, Allen D. Seftel, & Terry Hassold. (2004). Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex. Fertility and Sterility. 81(1). 205–209. 53 indexed citations

5.

Hassold, Terry, LuAnn Judis, E. Ricky Chan, et al.. (2004). Cytological studies of meiotic recombination in human males. Cytogenetic and Genome Research. 107(3-4). 249–255. 48 indexed citations

6.

Lynn, Audrey, Kara E. Koehler, LuAnn Judis, et al.. (2002). Covariation of Synaptonemal Complex Length and Mammalian Meiotic Exchange Rates. Science. 296(5576). 2222–2225. 216 indexed citations

7.

Hassold, Terry, Lindsay C. Burrage, E. Ricky Chan, et al.. (2001). Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction. The American Journal of Human Genetics. 69(2). 434–439. 58 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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