Cori Feist

411 total citations
13 papers, 209 citations indexed

About

Cori Feist is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Cori Feist has authored 13 papers receiving a total of 209 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pediatrics, Perinatology and Child Health, 5 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Cori Feist's work include Prenatal Screening and Diagnostics (7 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Cori Feist is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Cori Feist collaborates with scholars based in United States, Austria and Canada. Cori Feist's co-authors include Jamie O. Lo, Aaron B. Caughey, Brian L Shaffer, Kathryn L. Berrier, Diane Masser‐Frye, Blythe G. Crissman, Danielle LaGrave, Mary E. Norton, Susan L. Sell and Campbell K. Brasington and has published in prestigious journals such as SHILAP Revista de lepidopterología, Obstetrics and Gynecology and Atherosclerosis.

In The Last Decade

Cori Feist

11 papers receiving 186 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cori Feist United States	6	123	54	38	35	29	13	209
Campbell K. Brasington United States	6	310 2.5×	119 2.2×	61 1.6×	78 2.2×	60 2.1×	8	421
Rachel S. Fisher United States	9	89 0.7×	73 1.4×	37 1.0×	35 1.0×	28 1.0×	35	232
Laura Prescott United Kingdom	6	15 0.1×	62 1.1×	14 0.4×	64 1.8×	44 1.5×	10	235
Brandon Bankowski United States	9	302 2.5×	63 1.2×	246 6.5×	7 0.2×	41 1.4×	10	457
Danielle LaGrave United States	8	200 1.6×	129 2.4×	56 1.5×	30 0.9×	51 1.8×	11	327
Jennifer Eccles United States	6	182 1.5×	113 2.1×	71 1.9×	19 0.5×	83 2.9×	11	316
Jorien Seggers Netherlands	12	291 2.4×	22 0.4×	79 2.1×	14 0.4×	26 0.9×	23	325
Gordon Baker Australia	14	141 1.1×	105 1.9×	336 8.8×	12 0.3×	109 3.8×	19	714
Debra Abrams United States	5	29 0.2×	92 1.7×	38 1.0×	9 0.3×	29 1.0×	10	183
Fiona L. Mackie United Kingdom	10	144 1.2×	22 0.4×	23 0.6×	6 0.2×	15 0.5×	21	247

Countries citing papers authored by Cori Feist

Since Specialization

Citations

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

Fields of papers citing papers by Cori Feist

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cori Feist

This figure shows the co-authorship network connecting the top 25 collaborators of Cori Feist. A scholar is included among the top collaborators of Cori Feist 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 Cori Feist. Cori Feist 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

Feist, Cori, et al.. (2023). Prenatal Diagnosis of Micrognathia. NeoReviews. 24(11). e753–e762.

Feist, Cori, et al.. (2021). Prenatal Diagnosis of a Lethal Skeletal Dysplasia. NeoReviews. 22(12). e859–e865. 1 indexed citations

Feist, Cori, et al.. (2021). Depression and socioeconomic stressors in expectant parents with fetal congenital anomalies. The Journal of Maternal-Fetal & Neonatal Medicine. 35(25). 8645–8651. 12 indexed citations

Fitzgerald, Jamie, et al.. (2020). A Deep Intronic Variant Activates a Pseudoexon in the <b><i>MTM1</i></b>Gene in a Family with X-Linked Myotubular Myopathy. Molecular Syndromology. 11(5-6). 264–270. 5 indexed citations

Kahlfuß, Sascha, Ulrike Kaufmann, Axel R. Concepcion, et al.. (2020). STIM1‐mediated calcium influx controls antifungal immunity and the metabolic function of non‐pathogenic Th17 cells. EMBO Molecular Medicine. 12(8). e11592–e11592. 33 indexed citations

Hofbauer, Thomas M., Anna S. Ondracek, Cori Feist, et al.. (2020). Cathepsin G bypasses the classic renin angiotensin system, leading to enhanced neutrophil extracellular trap formation. Atherosclerosis. 315. e123–e123. 1 indexed citations

Feist, Cori, et al.. (2019). Monozygotic dichorionic diamniotic twins with large interstitial deletion of chromosome 1p. SHILAP Revista de lepidopterología. 7(9). 1735–1740. 3 indexed citations

Feist, Cori, et al.. (2016). Novel compound heterozygous mutations in inositol polyphosphate phosphatase-like 1 in a family with severe opsismodysplasia. Clinical Dysmorphology. 25(4). 152–155. 7 indexed citations

Lo, Jamie O., et al.. (2015). Jacobsen Syndrome Detected by Noninvasive Prenatal Testing. Obstetrics and Gynecology. 125(2). 387–389. 2 indexed citations

10.

Lo, Jamie O., Brian L Shaffer, Cori Feist, & Aaron B. Caughey. (2014). Chromosomal Microarray Analysis and Prenatal Diagnosis. Obstetrical & Gynecological Survey. 69(10). 613–621. 29 indexed citations

11.

Lo, Jamie O., Cori Feist, Mary E. Norton, & Aaron B. Caughey. (2014). Noninvasive Prenatal Testing. Obstetrical & Gynecological Survey. 69(2). 89–99. 31 indexed citations

12.

Marshall, Nicole, et al.. (2011). Chorionic villus sampling for abnormal screening compared to historical indications: prevalence of abnormal karyotypes. The Journal of Maternal-Fetal & Neonatal Medicine. 25(8). 1463–1466. 1 indexed citations

13.

Berrier, Kathryn L., Blythe G. Crissman, Cori Feist, et al.. (2011). Practice Guidelines for Communicating a Prenatal or Postnatal Diagnosis of Down Syndrome: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 20(5). 432–441. 84 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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