Jennifer Keller‐Ramey

607 total citations
8 papers, 162 citations indexed

About

Jennifer Keller‐Ramey is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jennifer Keller‐Ramey has authored 8 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jennifer Keller‐Ramey's work include Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Syndromes and Imprinting (1 paper). Jennifer Keller‐Ramey is often cited by papers focused on Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Syndromes and Imprinting (1 paper). Jennifer Keller‐Ramey collaborates with scholars based in United States, Australia and Germany. Jennifer Keller‐Ramey's co-authors include Carrie Fitzpatrick, Kerstin Kutsche, Ganka Douglas, Philippe M. Campeau, Thomas Krausz, Julie Scuffins, Christiane K. Bauer, Wickii T. Vigneswaran, James McElherne and Fernando Santos‐Simarro and has published in prestigious journals such as The American Journal of Human Genetics, Human Pathology and Genetics in Medicine.

In The Last Decade

Jennifer Keller‐Ramey

8 papers receiving 161 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer Keller‐Ramey United States	8	71	62	41	24	21	8	162
Cara Skraban United States	10	106 1.5×	120 1.9×	27 0.7×	45 1.9×	43 2.0×	31	244
Elaine M. Pereira United States	8	68 1.0×	100 1.6×	18 0.4×	35 1.5×	18 0.9×	24	191
М. В. Голубенко Russia	9	97 1.4×	87 1.4×	23 0.6×	10 0.4×	21 1.0×	53	237
Annamaria Perri Italy	9	128 1.8×	128 2.1×	25 0.6×	11 0.5×	23 1.1×	17	227
Haruka Hamanoue Japan	10	118 1.7×	84 1.4×	21 0.5×	33 1.4×	12 0.6×	23	220
Stefano Petrocchi Italy	8	84 1.2×	129 2.1×	16 0.4×	16 0.7×	31 1.5×	15	236
J. J. T. van Harssel Netherlands	5	70 1.0×	35 0.6×	25 0.6×	13 0.5×	10 0.5×	5	102
Moumita Biswas India	7	84 1.2×	42 0.7×	25 0.6×	7 0.3×	8 0.4×	11	208
Özgür Kırbıyık Türkiye	8	109 1.5×	83 1.3×	8 0.2×	31 1.3×	28 1.3×	40	211
Tomi L. Toler United States	7	105 1.5×	139 2.2×	58 1.4×	50 2.1×	23 1.1×	10	275

Countries citing papers authored by Jennifer Keller‐Ramey

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Keller‐Ramey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer Keller‐Ramey. 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 Jennifer Keller‐Ramey. The network helps show where Jennifer Keller‐Ramey may publish in the future.

Co-authorship network of co-authors of Jennifer Keller‐Ramey

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

All Works

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8 of 8 papers shown

Scuffins, Julie, Jennifer Keller‐Ramey, Ganka Douglas, et al.. (2021). Uniparental disomy in a population of 32,067 clinical exome trios. Genetics in Medicine. 23(6). 1101–1107. 38 indexed citations

Cross, Laura, Kirsty McWalter, Jennifer Keller‐Ramey, Lindsay B. Henderson, & Shivarajan Amudhavalli. (2020). A report of gonadal mosaicism in DHX30-related neurodevelopmental disorder. Clinical Dysmorphology. 29(3). 161–164. 7 indexed citations

Bauer, Christiane K., Fanny Kortüm, Janine Altmüller, et al.. (2019). Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome. The American Journal of Human Genetics. 104(6). 1139–1157. 40 indexed citations

Keller‐Ramey, Jennifer, Amy Knight Johnson, Jennifer A. Lee, et al.. (2017). Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome. Journal of Human Genetics. 63(3). 349–356. 10 indexed citations

McGregor, Stephanie M., James McElherne, Jennifer Keller‐Ramey, et al.. (2016). BAP1 immunohistochemistry has limited prognostic utility as a complement of CDKN2A (p16) fluorescence in situ hybridization in malignant pleural mesothelioma. Human Pathology. 60. 86–94. 33 indexed citations

Keller‐Ramey, Jennifer, Carrie Fitzpatrick, Sabah Kadri, et al.. (2016). Unclassified renal cell carcinoma with tubulopapillary architecture, clear cell phenotype, and chromosome 8 monosomy: a new kid on the block. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 469(1). 81–91. 11 indexed citations

Alkorta‐Aranburu, Gorka, Madina Sukhanova, David Carmody, et al.. (2016). Improved molecular diagnosis of patients with neonatal diabetes using a combined next-generation sequencing and MS-MLPA approach. Journal of Pediatric Endocrinology and Metabolism. 29(5). 523–531. 16 indexed citations

Shao, Lina, Sue Miller, Jennifer Keller‐Ramey, Yang Zhang, & Diane Roulston. (2015). Cytogenetic, fluorescence in situ hybridization, and genomic array characterization of chronic myeloid leukemia with cryptic BCR-ABL1 fusions. Cancer Genetics. 208(7-8). 396–403. 7 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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