Melissa Andrew

688 total citations
14 papers, 353 citations indexed

About

Melissa Andrew is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Melissa Andrew has authored 14 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Endocrinology, Diabetes and Metabolism and 7 papers in Genetics. Recurrent topics in Melissa Andrew's work include Growth Hormone and Insulin-like Growth Factors (7 papers), Genetic Syndromes and Imprinting (3 papers) and Thyroid Disorders and Treatments (3 papers). Melissa Andrew is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (7 papers), Genetic Syndromes and Imprinting (3 papers) and Thyroid Disorders and Treatments (3 papers). Melissa Andrew collaborates with scholars based in United States, Brazil and China. Melissa Andrew's co-authors include Andrew Dauber, Vivian Hwa, Kristine M. Wiren, Clare Wilhelm, Joel G. Hashimoto, Masanobu Fujimoto, David Haig, Matthew T. Weirauch, Ana Paula Abreu and Rona S. Carroll and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Endocrinology and The American Journal of Human Genetics.

In The Last Decade

Melissa Andrew

13 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Melissa Andrew United States	9	152	142	96	92	52	14	353
Samantha Sperduti Italy	13	119 0.8×	71 0.5×	126 1.3×	51 0.6×	26 0.5×	33	361
Anna‐Karin Norlén Sweden	4	99 0.7×	99 0.7×	64 0.7×	88 1.0×	11 0.2×	7	316
Chi‐Kuang Leo Wang Taiwan	11	181 1.2×	139 1.0×	18 0.2×	47 0.5×	21 0.4×	15	334
Sadahiro Ito Japan	7	125 0.8×	176 1.2×	106 1.1×	66 0.7×	9 0.2×	10	385
Davelene D. Israel United States	10	99 0.7×	56 0.4×	210 2.2×	36 0.4×	32 0.6×	10	506
Ichiro Miyata Japan	13	112 0.7×	98 0.7×	29 0.3×	133 1.4×	36 0.7×	36	407
S Stone United States	10	127 0.8×	41 0.3×	39 0.4×	196 2.1×	43 0.8×	12	406
Kristen R. Vella United States	13	167 1.1×	94 0.7×	36 0.4×	284 3.1×	19 0.4×	25	587
Mukesh Varshney Sweden	11	101 0.7×	63 0.4×	24 0.3×	23 0.3×	14 0.3×	24	275
Michaël W. Pankhurst New Zealand	16	144 0.9×	85 0.6×	400 4.2×	66 0.7×	52 1.0×	36	643

Countries citing papers authored by Melissa Andrew

Since Specialization

Citations

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

Fields of papers citing papers by Melissa Andrew

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melissa Andrew

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

All Works

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14 of 14 papers shown

Dauber, Andrew, et al.. (2023). Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency. Hormone Research in Paediatrics. 96(5). 449–457.

Andrew, Melissa, Seth Berger, Tricia Bhatti, et al.. (2022). Precocious Puberty in a Boy With Bilateral Leydig Cell Tumors due to a Somatic Gain-of-Function LHCGR Variant. Journal of the Endocrine Society. 6(10). bvac127–bvac127. 4 indexed citations

Dauber, Andrew, et al.. (2021). Treatment of Short Stature in Aggrecan-deficient Patients With Recombinant Human Growth Hormone: 1-Year Response. The Journal of Clinical Endocrinology & Metabolism. 107(5). e2103–e2109. 9 indexed citations

Fujimoto, Masanobu, Melissa Andrew, & Andrew Dauber. (2020). Disorders caused by genetic defects associated with GH-dependent genes: PAPPA2 defects. Molecular and Cellular Endocrinology. 518. 110967–110967. 12 indexed citations

Fujimoto, Masanobu, Melissa Andrew, Dongsheng Zhang, et al.. (2019). Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation. Endocrinology. 160(6). 1363–1376. 14 indexed citations

Hawkes, Colin P., Melissa Andrew, Diego Campos, et al.. (2019). Targeted Searches of the Electronic Health Record and Genomics Identify an Etiology in Three Patients with Short Stature and High IGF-I Levels. Hormone Research in Paediatrics. 92(3). 186–195. 5 indexed citations

Smolarek, Teresa A., et al.. (2019). Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome. The Journal of Pediatrics. 216. 227–231. 4 indexed citations

Andrew, Melissa, et al.. (2018). PAPPA2 as a Therapeutic Modulator of IGF-I Bioavailability: in Vivo and in Vitro Evidence. Journal of the Endocrine Society. 2(7). 646–656. 17 indexed citations

Dauber, Andrew, Marina Cunha-Silva, Delanie B. Macedo, et al.. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. The Journal of Clinical Endocrinology & Metabolism. 102(5). 1557–1567. 142 indexed citations

10.

Mizuno, Tomoyuki, Melissa Andrew, Alexander A. Vinks, et al.. (2017). Pharmacokinetics of IGF-1 in PAPP-A2-Deficient Patients, Growth Response, and Effects on Glucose and Bone Density. The Journal of Clinical Endocrinology & Metabolism. 102(12). 4568–4577. 27 indexed citations

11.

Boyle, Lia, Mirjam M. C. Wamelink, Gajja S. Salomons, et al.. (2016). Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects. The American Journal of Human Genetics. 98(6). 1235–1242. 33 indexed citations

12.

Bruin, Christiaan de, Zerrin Orbak, Melissa Andrew, Vivian Hwa, & Andrew Dauber. (2016). Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 Deficiency. Hormone Research in Paediatrics. 85(5). 358–362. 5 indexed citations

13.

Bruin, Christiaan de, Courtney Finlayson, Mariana F.A. Funari, et al.. (2016). Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia. Hormone Research in Paediatrics. 86(5). 342–348. 21 indexed citations

14.

Wilhelm, Clare, et al.. (2015). Astrocyte Dysfunction Induced by Alcohol in Females but Not Males. Brain Pathology. 26(4). 433–451. 60 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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