Melissa Crenshaw

825 total citations
13 papers, 83 citations indexed

About

Melissa Crenshaw is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Melissa Crenshaw has authored 13 papers receiving a total of 83 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Melissa Crenshaw's work include Congenital heart defects research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetic factors in colorectal cancer (2 papers). Melissa Crenshaw is often cited by papers focused on Congenital heart defects research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetic factors in colorectal cancer (2 papers). Melissa Crenshaw collaborates with scholars based in United States, Denmark and Venezuela. Melissa Crenshaw's co-authors include Harry C. Dietz, Kathleen C. Kent, Denise Goh, Michelle S. Miller, Angela E. Lin, Laurence Faivre, Ingrid M. Wentzensen, Stanley Iyadurai, Antonio Vitobello and Christel Thauvin‐Robinet and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Thoracic and Cardiovascular Surgery and Neuro-Oncology.

In The Last Decade

Melissa Crenshaw

9 papers receiving 82 citations

Peers

Melissa Crenshaw

GENET

PRM

CCM

PPCH

Juha Hartikainen Finland

Katharina Löhner Netherlands

María Eugenia Rocha Germany

Henrike Krenz Germany

Eddie Ip Australia

Ljubica Odak Croatia

Sara Caylor United States

Lamisse Mansour‐Hendili France

Sophie Debrus Germany

Joanna Lazier Canada

Juha Hartikainen Finland

Melissa Crenshaw

63 ×1.8

GENET

21 ×0.6

PRM

39 ×1.4

45 ×2.0

CCM

7 ×0.5

PPCH

Citations per year, relative to Melissa Crenshaw Melissa Crenshaw (= 1×) peers Juha Hartikainen

Countries citing papers authored by Melissa Crenshaw

Since Specialization

Citations

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

Fields of papers citing papers by Melissa Crenshaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melissa Crenshaw

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

Bedei, Ivonne, Ida Charlotte Bay Lund, Ida Vogel, et al.. (2025). Non‐Invasive Prenatal Testing by Cell‐Free DNA ( cfNIPT ) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal Outcomes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 199(2). 124–133.

Álvarez‐Nava, Francisco, et al.. (2025). The Impact of Karyotype on Congenital Heart Diseases in Turner Syndrome: A Systematic Review and Meta‐Analysis. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 199(2). 93–106.

Fritz, Alyssa, et al.. (2025). Autism Spectrum Disorder in the Cleft Population: Evaluating Occurrence in Non-Syndromic Patients. The Cleft Palate-Craniofacial Journal. 299955411–299955411.

Geller, Thomas J., et al.. (2022). Hypotonic infant with PURA syndrome-related channelopathy successfully treated with pyridostigmine. Neuromuscular Disorders. 32(2). 166–169. 6 indexed citations

Assoum, Mirna, Ange‐Line Bruel, Melissa Crenshaw, et al.. (2020). NovelKIAA1033/WASHC4mutations in three patients with syndromic intellectual disability and a review of the literature. American Journal of Medical Genetics Part A. 182(4). 792–797. 10 indexed citations

Crenshaw, Melissa, et al.. (2019). A patient with Phelan‐McDermid syndrome and dilation of the great vessels. SHILAP Revista de lepidopterología. 7(4). 607–611. 5 indexed citations

Prakash, Siddharth K., et al.. (2019). “Donating our bodies to science”: A discussion about autopsy and organ donation in Turner syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(1). 22–28. 3 indexed citations

Prakash, Siddharth K., Rebecca Knickmeyer, Melissa Crenshaw, et al.. (2019). The Turner syndrome research registry: Creating equipoise between investigators and participants. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(1). 7–12. 15 indexed citations

Oshrine, Benjamin, Melissa Crenshaw, Melissa Edwards, et al.. (2019). B-cell acute lymphoblastic leukemia with high mutation burden presenting in a child with constitutional mismatch repair deficiency. Blood Advances. 3(12). 1795–1798. 5 indexed citations

10.

Lukas, Claudia, Melissa Crenshaw, Ignacio González-Gómez, et al.. (2018). MBCL-46. COMPOUND HETEROZYGOUS MUTATION OF THE PMS2 GENE IN AN INFANT WITH CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY AND MEDULLOBLASTOMA. Neuro-Oncology. 20(suppl_2). i127–i127. 1 indexed citations

11.

Goldmuntz, Elizabeth, Melissa Crenshaw, & Angela E. Lin. (2013). Genetic aspects of congenital heart defects. 4 indexed citations

12.

Kent, Kathleen C., Melissa Crenshaw, Denise Goh, & Harry C. Dietz. (2012). Genotype–phenotype correlation in patients with bicuspid aortic valve and aneurysm. Journal of Thoracic and Cardiovascular Surgery. 146(1). 158–165.e1. 33 indexed citations

13.

Patel, Anil Kumar, et al.. (2009). Identity propagation in N-tier systems. 1–5. 1 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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