Ann Garber

870 total citations
13 papers, 619 citations indexed

About

Ann Garber is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Ann Garber has authored 13 papers receiving a total of 619 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in Ann Garber's work include Connective tissue disorders research (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic Syndromes and Imprinting (3 papers). Ann Garber is often cited by papers focused on Connective tissue disorders research (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic Syndromes and Imprinting (3 papers). Ann Garber collaborates with scholars based in United States, Australia and Canada. Ann Garber's co-authors include David Sillence, David L. Rimoin, D L Rimoin, Judith G. Hall, Sascha Dietrich, John M. Opitz, William G. Cole, James F. Reynolds, H. Craig Heller and Ralph J. Berger and has published in prestigious journals such as Science, The American Journal of Human Genetics and Genomics.

In The Last Decade

Ann Garber

13 papers receiving 599 citations

Peers

Ann Garber
James V. Higgins United States
Kirsten Rasmussen Denmark
M D Crawfurd United Kingdom
Roberto Lala Italy
Talaat I. Farag Kuwait
Erawati V. Bawle United States
Robert Wallerstein United States
Clare V. Logan United Kingdom
Harold Chen United States
Miroslav Mayer Croatia
James V. Higgins United States
Ann Garber
Citations per year, relative to Ann Garber Ann Garber (= 1×) peers James V. Higgins

Countries citing papers authored by Ann Garber

Since Specialization
Citations

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

Fields of papers citing papers by Ann Garber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Garber

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

All Works

13 of 13 papers shown
1.
McCarty, Catherine A., Ann Garber, Jonathan C. Reeser, & Norman Fost. (2011). Study newsletters, community and ethics advisory boards, and focus group discussions provide ongoing feedback for a large biobank. American Journal of Medical Genetics Part A. 155(4). 737–741. 38 indexed citations
2.
Krakow, Deborah, Kent A. Reinker, Berkley R. Powell, et al.. (1998). Localization of a Multiple Synostoses–Syndrome Disease Gene to Chromosome 17q21-22. The American Journal of Human Genetics. 63(1). 120–124. 41 indexed citations
3.
Mao, Rong, Elizabeth Berry‐Kravis, Ann Garber, et al.. (1998). Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases. American Journal of Medical Genetics. 80(5). 473–480. 30 indexed citations
4.
Rimoin, David L., Michael D. Briggs, Peter J. Roughley, et al.. (1994). A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix. Human Genetics. 93(3). 236–242. 33 indexed citations
5.
Garber, Ann, et al.. (1994). Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16. Prenatal Diagnosis. 14(4). 257–266. 27 indexed citations
6.
Briggs, Michael D., Matthew L. Warman, John Loughlin, et al.. (1994). Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM 2) to a region of chromosome 1 containing a type IX collagen gene. Matrix Biology. 14(5). 399–399. 27 indexed citations
7.
Bacino, Carlos A., Lawrence D. Platt, Ann Garber, et al.. (1993). Fetal akinesia/hypokinesia sequence: Prenatal diagnosis and intra‐familial variability. Prenatal Diagnosis. 13(11). 1011–1019. 8 indexed citations
8.
Briggs, Michael D., James L. Weber, Juliet Yuen, et al.. (1993). Genetic linkage of mild pseudoachondroplasia (PSACH) to markersin the pericentromeric region of chromosome 19. Genomics. 18(3). 656–660. 42 indexed citations
9.
Sharony, Reuven, Ann Garber, David Viskochil, et al.. (1993). Preaxial ray reduction defects as part of valproic acid embryofetopathy. Prenatal Diagnosis. 13(10). 909–918. 42 indexed citations
10.
Garber, Ann, et al.. (1990). Prenatal Genetic Counseling. Clinics in Perinatology. 17(4). 749–759. 7 indexed citations
11.
Sillence, David, William G. Cole, Sascha Dietrich, et al.. (1986). Osteogenesis imperfecta type III. Delineation of the phenotype with reference to genetic heterogeneity. American Journal of Medical Genetics. 23(3). 821–832. 153 indexed citations
12.
Sillence, David, et al.. (1984). Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity. American Journal of Medical Genetics. 17(2). 407–423. 118 indexed citations
13.
Walker, James M., Ann Garber, Ralph J. Berger, & H. Craig Heller. (1979). Sleep and Estivation (Shallow Torpor): Continuous Processes of Energy Conservation. Science. 204(4397). 1098–1100. 53 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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