Jeanette C. Ramer

991 total citations
25 papers, 584 citations indexed

About

Jeanette C. Ramer is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Jeanette C. Ramer has authored 25 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Jeanette C. Ramer's work include Genomic variations and chromosomal abnormalities (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Congenital limb and hand anomalies (3 papers). Jeanette C. Ramer is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Congenital limb and hand anomalies (3 papers). Jeanette C. Ramer collaborates with scholars based in United States, Italy and France. Jeanette C. Ramer's co-authors include Roger L. Ladda, Geoffrey Miller, Javad Towfighi, Lucas R. Celant, Barry G. Baylen, Richard S. Young, Philip N. Mowrey, Angela E. Lin, Robin Winter and R Pallotta and has published in prestigious journals such as Anesthesiology, Acta Neuropathologica and Journal of Medical Genetics.

In The Last Decade

Jeanette C. Ramer

25 papers receiving 567 citations

Peers

Jeanette C. Ramer

GENET

PPCH

PMH

EPIDE

Mary A. Murphy United States

Javier López Pisón Spain

James Q. Miller United States

D Fontan France

Aron J. Diament Brazil

Joseph Peeden United States

Catherine Sarret France

Marie-Odile Livet France

Lawrence T. Taft United States

Matteo Della Monica Italy

Mary A. Murphy United States

Jeanette C. Ramer

262 ×1.2

GENET

182 ×0.9

41 ×0.4

PPCH

141 ×1.5

PMH

70 ×0.9

EPIDE

Citations per year, relative to Jeanette C. Ramer Jeanette C. Ramer (= 1×) peers Mary A. Murphy

Countries citing papers authored by Jeanette C. Ramer

Since Specialization

Citations

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

Fields of papers citing papers by Jeanette C. Ramer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeanette C. Ramer. 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 Jeanette C. Ramer. The network helps show where Jeanette C. Ramer may publish in the future.

Co-authorship network of co-authors of Jeanette C. Ramer

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

All Works

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20 of 20 papers shown

Schengrund, Cara‐Lynne, et al.. (2012). Cholesterol, GM1, and Autism. Neurochemical Research. 37(6). 1201–1207. 27 indexed citations

Miller, Geoffrey, et al.. (1996). Outcome After Open-Heart Surgery in Infants and Children. Journal of Child Neurology. 11(1). 49–53. 71 indexed citations

Ramer, Jeanette C., Angela E. Lin, William B. Dobyns, et al.. (1995). Previously apparently undescribed syndrome: Shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation. American Journal of Medical Genetics. 57(3). 403–409. 82 indexed citations

Hess, Ellen J., et al.. (1995). Absence of linkage of apparently single gene mediated ADHD with the human syntenic region of the mouse mutantColoboma. American Journal of Medical Genetics. 60(6). 573–579. 50 indexed citations

Ladda, Roger L., Jonathan Zonana, Jeanette C. Ramer, Maria J. Mascari, & Peter K. Rogan. (1993). Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: A distinct syndrome. American Journal of Medical Genetics. 47(4). 550–555. 5 indexed citations

Ramer, Jeanette C., et al.. (1993). Identical twins with Weissenbacher‐Zweymüller syndrome and neural tube defect. American Journal of Medical Genetics. 45(5). 614–618. 7 indexed citations

Ramer, Jeanette C., et al.. (1993). Marden‐Walker phenotype: Spectrum of variability in three infants. American Journal of Medical Genetics. 45(3). 285–291. 14 indexed citations

Miller, Geoffrey & Jeanette C. Ramer. (1992). Static encephalopathies of infancy and childhood. Raven Press eBooks. 10 indexed citations

Eggli, Kathleen D., et al.. (1992). Melnick-Needles syndrome. Pediatric Radiology. 22(4). 257–261. 11 indexed citations

10.

Ramer, Jeanette C., et al.. (1992). Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in child. American Journal of Medical Genetics. 44(2). 197–199. 1 indexed citations

11.

Ramer, Jeanette C., et al.. (1992). Syndrome identification #149: Trigonocephaly, pachygyria, retinal coloboma, and cardiac defect: A distinct syndrome. 6(1). 15–20. 4 indexed citations

12.

Ramer, Jeanette C., et al.. (1991). Phenotypic variation of multiple pterygium syndrome in siblings, including identical twins. 5(4). 97–106. 4 indexed citations

13.

Ramer, Jeanette C., Philip N. Mowrey, & Roger L. Ladda. (1991). Malformations in a child with dup (7 pter‐p15.1) and del (7 q36‐qter) as a result of familial pericentric inversion. Clinical Genetics. 39(6). 442–450. 10 indexed citations

14.

Ramer, Jeanette C., et al.. (1990). Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: Review of brain, cardiac, and limb malformations. American Journal of Medical Genetics. 37(3). 392–400. 57 indexed citations

15.

Ramer, Jeanette C., et al.. (1989). Two infants with del(3)(p25pter) and a review of previously reported cases. American Journal of Medical Genetics. 33(1). 108–112. 21 indexed citations

16.

Ramer, Jeanette C., et al.. (1989). A review of phenotype‐karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2. American Journal of Medical Genetics. 32(3). 359–363. 34 indexed citations

17.

Ramer, Jeanette C. & Roger L. Ladda. (1989). Humero‐radial synostosis with ulnar defects in sibs. American Journal of Medical Genetics. 33(2). 176–179. 7 indexed citations

18.

Ramer, Jeanette C.. (1988). Multiple Pterygium Syndrome. American journal of diseases of children. 142(7). 794–794. 12 indexed citations

19.

Young, Richard S., et al.. (1985). Magnetic resonance imaging in leukodystrophies of childhood. Pediatric Neurology. 1(1). 15–19. 22 indexed citations

20.

Kofke, W. Andrew, Michael T. Snider, Richard S. Young, & Jeanette C. Ramer. (1985). Prolonged Low Flow Isoflurane Anesthesia for Status Epilepticus. Anesthesiology. 62(5). 653–656. 42 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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