Ferrin C. Wheeler

534 total citations
16 papers, 314 citations indexed

About

Ferrin C. Wheeler is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Ferrin C. Wheeler has authored 16 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Ferrin C. Wheeler's work include Cancer Genomics and Diagnostics (3 papers), Prenatal Screening and Diagnostics (2 papers) and MicroRNA in disease regulation (2 papers). Ferrin C. Wheeler is often cited by papers focused on Cancer Genomics and Diagnostics (3 papers), Prenatal Screening and Diagnostics (2 papers) and MicroRNA in disease regulation (2 papers). Ferrin C. Wheeler collaborates with scholars based in United States, Italy and Indonesia. Ferrin C. Wheeler's co-authors include Douglas A. Marchuk, Gregory LaMonte, Sehoon Keum, Surovi Hazarika, Yongjun Li, Ayotunde O. Dokun, Brian H. Annex, Howard A. Rockman, Hao Tang and Lan Mao and has published in prestigious journals such as Circulation, Nature Communications and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Ferrin C. Wheeler

16 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ferrin C. Wheeler United States	7	178	82	65	63	44	16	314
Takefumi Oka Japan	9	147 0.8×	151 1.8×	56 0.9×	46 0.7×	26 0.6×	21	293
Brigitte Spath Germany	8	134 0.8×	35 0.4×	38 0.6×	35 0.6×	33 0.8×	14	401
Cassandra P. Loren United States	7	111 0.6×	68 0.8×	36 0.6×	31 0.5×	16 0.4×	8	342
Yoshiki Sawa Japan	8	115 0.6×	47 0.6×	136 2.1×	88 1.4×	27 0.6×	9	358
Laurence Servais Belgium	7	91 0.5×	105 1.3×	33 0.5×	28 0.4×	77 1.8×	10	256
Rebecca Teske United States	6	210 1.2×	69 0.8×	151 2.3×	39 0.6×	125 2.8×	9	385
Sander M. van de Weg Netherlands	9	115 0.6×	95 1.2×	54 0.8×	41 0.7×	64 1.5×	11	318
Martina Morowski Germany	9	59 0.3×	54 0.7×	62 1.0×	22 0.3×	22 0.5×	10	319
Song Gu China	11	185 1.0×	150 1.8×	161 2.5×	50 0.8×	116 2.6×	35	389
Wen Yuan China	12	232 1.3×	48 0.6×	50 0.8×	25 0.4×	155 3.5×	28	368

Countries citing papers authored by Ferrin C. Wheeler

Since Specialization

Citations

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

Fields of papers citing papers by Ferrin C. Wheeler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ferrin C. Wheeler

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

All Works

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16 of 16 papers shown

Schuler, Bryce, et al.. (2023). Collaborative efforts to improve genetic testing in the neonatal intensive care unit. Journal of Perinatology. 43(12). 1500–1505. 2 indexed citations

Wheeler, Ferrin C., et al.. (2022). 33. Variability in sex and phenotype: Impact of a familial pathogenic DHX37 variant leading to 46,XY gonadal dysgenesis. Cancer Genetics. 264-265. 11–11. 1 indexed citations

Shaver, Timothy M., Hailing Jin, Clayton B. Marshall, et al.. (2021). Acquisition of aneuploidy drives mutant p53-associated gain-of-function phenotypes. Nature Communications. 12(1). 5184–5184. 35 indexed citations

Smith, Rebecca B., et al.. (2021). Clinical diagnosis of neurofibromatosis type I in multiple family members due to cosegregation of a unique balanced translocation with disruption of the NF1 locus: Testing considerations for accurate diagnosis. American Journal of Medical Genetics Part A. 185(4). 1222–1227. 2 indexed citations

Colby, Jennifer M., Ferrin C. Wheeler, Kimberly A. Petrie, Kathleen L. Gould, & Jonathan E. Schmitz. (2020). Institutional Training Opportunities for PhD Students in Laboratory Medicine: An Unmet Career Development Need?. The Journal of Applied Laboratory Medicine. 5(2). 412–416. 2 indexed citations

Carson, Robert P., Lynne M. Bird, Anna K. Childers, Ferrin C. Wheeler, & Jessica Duis. (2019). Preserved expressive language as a phenotypic determinant of Mosaic Angelman Syndrome. Molecular Genetics & Genomic Medicine. 7(9). e837–e837. 12 indexed citations

Vischini, Gisella, Meghan Kapp, Ferrin C. Wheeler, Laszlo Hopp, & Agnes B. Fogo. (2018). A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome. Human Pathology. 81. 229–234. 6 indexed citations

Wheeler, Ferrin C., Annette S. Kim, Claudio A. Mosse, et al.. (2018). Limited Utility of Fluorescence In Situ Hybridization for Recurrent Abnormalities in Acute Myeloid Leukemia at Diagnosis and Follow-up. American Journal of Clinical Pathology. 149(5). 418–424. 9 indexed citations

Wheeler, Ferrin C., et al.. (2018). Lack of MDM2 interpretation guidelines contribute to diagnostic difficulty in a case of undifferentiated sarcoma. Human Pathology Case Reports. 13. 1–3. 2 indexed citations

10.

Wang, Xuan J., Gabriel K. Griffin, Ashwini Yenamandra, et al.. (2016). Transformation of follicular lymphoma into classical Hodgkin lymphoma showing t(14;18). 1(1). 2 indexed citations

11.

Lu, Yan, Megha Talati, Santhi Gladson, et al.. (2015). Bone Marrow-derived Cells Contribute to Pathogenesis of Pulmonary Arterial Hypertension.. American Journal of Respiratory and Critical Care Medicine. 2 indexed citations

12.

Ling, Yan, Xinping Chen, Megha Talati, et al.. (2015). Bone Marrow–derived Cells Contribute to the Pathogenesis of Pulmonary Arterial Hypertension. American Journal of Respiratory and Critical Care Medicine. 193(8). 898–909. 53 indexed citations

13.

Yenamandra, Ashwini, et al.. (2014). Detection of Genomic Imbalances Involved in Common Chromosomal Rearrangements of Acute Leukemia by Cytogenomic SNP Microarray Analysis. Cancer Genetics. 207(6). 289–290. 3 indexed citations

14.

Wheeler, Ferrin C., Hao Tang, Tracy N. Hadnott, et al.. (2009). Tnni3k Modifies Disease Progression in Murine Models of Cardiomyopathy. PLoS Genetics. 5(9). e1000647–e1000647. 64 indexed citations

15.

Dokun, Ayotunde O., Sehoon Keum, Surovi Hazarika, et al.. (2008). A Quantitative Trait Locus (LSq-1) on Mouse Chromosome 7 Is Linked to the Absence of Tissue Loss After Surgical Hindlimb Ischemia. Circulation. 117(9). 1207–1215. 99 indexed citations

16.

Wheeler, Ferrin C., Liliana Fernández, Kerri M. Carlson, et al.. (2005). QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survival. Mammalian Genome. 16(6). 414–423. 20 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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