Elisabeth A. Keitges

774 citations

13 papers · 529 indexed · h-index 11

Co-authors: Stanley M. Gartler M. Siniscalco Daniel F. Schorderet Catherine G. Palmer Hiba Risheg Rachel D. Burnside Klaus Harbers Romela Pasion
Topics: Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers)Genomic variations and chromosomal abnormalities (5 papers)Estrogen and related hormone effects (4 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Reproductive Medicine
Journals: Nature Proceedings of the National Academy of Sciences Genetics
Partner nations: United States Qatar Australia

In The Last Decade

Elisabeth A. Keitges

13 papers receiving 487 citations

Peers

Countries citing papers authored by Elisabeth A. Keitges

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth A. Keitges

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elisabeth A. Keitges. 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 Elisabeth A. Keitges. The network helps show where Elisabeth A. Keitges may publish in the future.

Co-authorship network of co-authors of Elisabeth A. Keitges

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects 2013 ·American Journal of Medical Genetics Part A ·Elisabeth A. Keitges,Romela Pasion,Rachel D. Burnside,(unknown),Antonio Gonzalez‐Ruiz,Teresa Dunn,(unknown),Joseph A. Gebbia,Carlos O. Fernandez,Hiba Risheg	28
2	Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype 2013 ·American Journal of Medical Genetics Part A ·Rachel D. Burnside,John Pappas,Stephanie Sacharow,Carolyn Applegate,Ada Hamosh,Inder Gadi,Vikram Jaswaney,Elisabeth A. Keitges,Karen Phillips,(unknown),Hiba Risheg,Janice Smith,(unknown),Stuart Schwartz,Peter Papenhausen	30
3	Clinical Comparison of Overlapping Deletions of 19p13.3 2013 ·American Journal of Medical Genetics Part A ·Hiba Risheg,Romela Pasion,(unknown),Virginia K. Proud,LaDonna Immken,Stuart Schwartz,(unknown),Peter Papenhausen,Tiong Yang Tan,Joris Andrieux,Ghislaine Plessis,David J. Amor,Elisabeth A. Keitges	9
4	UPD detection using homozygosity profiling with a SNP genotyping microarray 2011 ·American Journal of Medical Genetics Part A ·Peter Papenhausen,Stuart Schwartz,Hiba Risheg,Elisabeth A. Keitges,Inder Gadi,Rachel D. Burnside,Vikram Jaswaney,John Pappas,Romela Pasion,Kenneth J. Friedman,James Tepperberg	115
5	Inactivation and reactivation of sex-linked steroid sulfatase gene in murine cell culture 1988 ·Somatic Cell and Molecular Genetics ·Daniel F. Schorderet,Elisabeth A. Keitges,Patrice Dubois,Stanley M. Gartler	13
6	Linkage of the Steroid Sulfatase Gene to the Sex-Reversed Mutation in the Mouse 1987 ·Genetics ·Elisabeth A. Keitges,Daniel F. Schorderet,Stanley M. Gartler	38
7	High-frequency reactivation of X-linked genes in chinese hamster � human hybrid cells 1987 ·Somatic Cell and Molecular Genetics ·Nathan A. Ellis,Elisabeth A. Keitges,Stanley M. Gartler,Mariano Rocchi	22
8	High rate of recombination and double crossovers in the mouse pseudoautosomal region during male meiosis. 1987 ·Proceedings of the National Academy of Sciences ·Philippe Soriano,Elisabeth A. Keitges,Daniel F. Schorderet,Klaus Harbers,Stanley M. Gartler,Rudolf Jaenisch	81
9	Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique 1986 ·Human Genetics ·Elisabeth A. Keitges,Catherine G. Palmer	38
10	Dosage of the Sts gene in the mouse. 1986 ·PubMed ·Elisabeth A. Keitges,Stanley M. Gartler	18
11	X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele 1985 ·Nature ·Elisabeth A. Keitges,(unknown),M. Siniscalco,Stanley M. Gartler	123
12	Prune belly syndrome in an anencephalic male 1983 ·American Journal of Medical Genetics ·M. E. Hodes,Merlin G. Butler,Elisabeth A. Keitges,L. David Mirkin,(unknown)	3
13	Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function 1982 ·Human Genetics ·Elisabeth A. Keitges,Catherine G. Palmer,David D. Weaver	11

About Elisabeth A. Keitges

Elisabeth A. Keitges is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism, having authored 13 papers that have together received 529 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Estrogen and related hormone effects (4 papers). The work is most often cited by research in Genetics (439 citations), Pediatrics, Perinatology and Child Health (85 citations) and Reproductive Medicine (35 citations). Elisabeth A. Keitges has collaborated with scholars based in United States, Qatar and Australia. Frequent co-authors include Stanley M. Gartler, M. Siniscalco, Daniel F. Schorderet, Catherine G. Palmer, Hiba Risheg, Rachel D. Burnside, Klaus Harbers, Romela Pasion, Rudolf Jaenisch and Philippe Soriano. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Genetics.

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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