Dinah Yaeger

1.9k total citations
9 papers, 840 citations indexed

About

Dinah Yaeger is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dinah Yaeger has authored 9 papers receiving a total of 840 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dinah Yaeger's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Chromatin Dynamics (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Dinah Yaeger is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Chromatin Dynamics (4 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Dinah Yaeger collaborates with scholars based in United States, Italy and Canada. Dinah Yaeger's co-authors include Maninder Kaur, Ian D. Krantz, Antonie D. Kline, Cheryl DeScipio, Jennifer McCallum, Laird G. Jackson, Marcella Devoto, Ian D. Krantz, Bart Loeys and Meredith Wilson and has published in prestigious journals such as The American Journal of Human Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Dinah Yaeger

9 papers receiving 820 citations

Peers

Dinah Yaeger

GENET

PPCH

PFM

Joanna Wiszniewska United States

Vanna Pecile Italy

Heidi A. Heilstedt United States

Anna Capalbo Italy

Jennifer McCallum United States

Eva Rossier Germany

Janice C. Palumbos United States

Maureen Holvoet Belgium

Brian P. Perry United States

Fanny Kortüm Germany

Joanna Wiszniewska United States

Dinah Yaeger

348 ×0.5

360 ×1.0

GENET

67 ×0.7

106 ×1.3

PPCH

15 ×0.3

PFM

Citations per year, relative to Dinah Yaeger Dinah Yaeger (= 1×) peers Joanna Wiszniewska

Countries citing papers authored by Dinah Yaeger

Since Specialization

Citations

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

Fields of papers citing papers by Dinah Yaeger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dinah Yaeger

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

All Works

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9 of 9 papers shown

DeScipio, Cheryl, Nancy B. Spinner, Maninder Kaur, et al.. (2008). Fine‐mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals. American Journal of Medical Genetics Part A. 146A(6). 730–739. 32 indexed citations

Deardorff, Matthew A., Maninder Kaur, Dinah Yaeger, et al.. (2007). Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation. The American Journal of Human Genetics. 80(3). 485–494. 385 indexed citations

Li, Yuelin, Annie G. Steinberg, Lisa J. Bain, et al.. (2007). Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultation. American Journal of Medical Genetics Part A. 143A(14). 1546–1553. 13 indexed citations

Kenna, Margaret A., Heidi L. Rehm, Caroline D. Robson, et al.. (2007). Additional clinical manifestations in children with sensorineural hearing loss and biallelicGJB2mutations: Who should be offeredGJB2testing?. American Journal of Medical Genetics Part A. 143A(14). 1560–1566. 22 indexed citations

Yaeger, Dinah, Jennifer McCallum, Kathleen Lewis, et al.. (2006). Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic. American Journal of Medical Genetics Part A. 140A(8). 827–836. 23 indexed citations

DeScipio, Cheryl, Lori Schneider, Terri L. Young, et al.. (2005). Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher?Schinzel (3C) syndrome. American Journal of Medical Genetics Part A. 134A(1). 3–11. 54 indexed citations

DeScipio, Cheryl, Maninder Kaur, Dinah Yaeger, et al.. (2005). Chromosome rearrangements in Cornelia de Lange syndrome (CdLS): Report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements. American Journal of Medical Genetics Part A. 137A(3). 276–282. 25 indexed citations

Kaur, Maninder, Cheryl DeScipio, Jennifer McCallum, et al.. (2005). Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 138A(1). 27–31. 73 indexed citations

Gillis, Lynette A., Jennifer McCallum, Maninder Kaur, et al.. (2004). NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations. The American Journal of Human Genetics. 75(4). 610–623. 213 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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