Melanie Manning

3.7k total citations · 2 hit papers
30 papers, 2.4k citations indexed

About

Melanie Manning is a scholar working on Pediatrics, Perinatology and Child Health, Rheumatology and Genetics. According to data from OpenAlex, Melanie Manning has authored 30 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pediatrics, Perinatology and Child Health, 9 papers in Rheumatology and 9 papers in Genetics. Recurrent topics in Melanie Manning's work include Prenatal Substance Exposure Effects (14 papers), Folate and B Vitamins Research (9 papers) and Gestational Diabetes Research and Management (8 papers). Melanie Manning is often cited by papers focused on Prenatal Substance Exposure Effects (14 papers), Folate and B Vitamins Research (9 papers) and Gestational Diabetes Research and Management (8 papers). Melanie Manning collaborates with scholars based in United States, South Africa and Italy. Melanie Manning's co-authors include Louanne Hudgins, Philip A. May, Luther K. Robinson, H. Eugene Hoyme, Wendy O. Kalberg, David Buckley, J. Phillip Gossage, Jason Blankenship, Julie M. Hasken and Margaret P Adam and has published in prestigious journals such as PEDIATRICS, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Melanie Manning

27 papers receiving 2.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Prevalence and epidemiologic characteristics of FASD from various research methods with an emphasis on recent in‐school studies

2009 641 citations Philip A. May, J. Phillip Gossage et al. PubMed profile →
Prevalence and Characteristics of Fetal Alcohol Spectrum Disorders

2014 424 citations Philip A. May, Jason Blankenship et al. PEDIATRICS profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Melanie Manning United States	19	1.8k	706	520	504	338	30	2.4k
Omar Abdul‐Rahman United States	25	1.2k 0.7×	541 0.8×	376 0.7×	484 1.0×	647 1.9×	69	2.4k
Melanie A. Manning United States	24	1.1k 0.6×	538 0.8×	310 0.6×	418 0.8×	435 1.3×	48	1.8k
John T. Martsolf United States	23	689 0.4×	268 0.4×	200 0.4×	411 0.8×	193 0.6×	38	1.2k
Arnold L. Christianson South Africa	19	435 0.2×	56 0.1×	64 0.1×	471 0.9×	366 1.1×	52	1.4k
V. Hesse Germany	23	316 0.2×	147 0.2×	63 0.1×	369 0.7×	373 1.1×	83	1.4k
Anne Hampton Australia	17	212 0.1×	192 0.3×	73 0.1×	103 0.2×	151 0.4×	20	1.4k
Marsha L. Davenport United States	27	422 0.2×	113 0.2×	39 0.1×	1.2k 2.3×	1.2k 3.4×	52	2.9k
Lavinia Gordon Australia	25	575 0.3×	309 0.4×	20 0.0×	614 1.2×	1.6k 4.7×	36	2.4k
Manuel Fernández Sánchez Spain	23	385 0.2×	318 0.5×	16 0.0×	185 0.4×	445 1.3×	90	2.3k
M Vanderschueren‐Lodeweyckx Belgium	27	454 0.2×	96 0.1×	23 0.0×	505 1.0×	811 2.4×	92	2.0k

Countries citing papers authored by Melanie Manning

Since Specialization

Citations

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

Fields of papers citing papers by Melanie Manning

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melanie Manning

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

Santoro, Jonathan D., et al.. (2024). Diagnostic abnormalities, disease severity and immunotherapy responsiveness in individuals with Down syndrome regression disorder. Scientific Reports. 14(1). 30865–30865. 1 indexed citations

May, Philip A., Barbara G. Tabachnick, Julie M. Hasken, et al.. (2024). Clinical Features of Typically Developing Children with and without Prenatal Alcohol Exposure. The Journal of Pediatrics. 281. 114327–114327.

Zhu, Wenjuan, et al.. (2023). Generation of two induced pluripotent stem cell lines from patients with Down syndrome. Stem Cell Research. 72. 103204–103204.

Blumenfeld, Yair J., Alexis S. Davis, Susan R. Hintz, et al.. (2016). Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal Period. Journal of Ultrasound in Medicine. 35(6). 1353–1358. 4 indexed citations

May, Philip A., Jason Blankenship, Wendy O. Kalberg, et al.. (2015). Prevalence and characteristics of fetal alcohol syndrome and partial fetal alcohol syndrome in a Rocky Mountain Region City. Drug and Alcohol Dependence. 155. 118–127. 55 indexed citations

Shamseldin, Hanan E., Anas M. Alazami, Melanie Manning, et al.. (2015). RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans. The American Journal of Human Genetics. 97(6). 862–868. 31 indexed citations

Ceccanti, Mauro, Daniela Fiorentino, Giovanna Coriale, et al.. (2014). Maternal risk factors for fetal alcohol spectrum disorders in a province in Italy. Drug and Alcohol Dependence. 145. 201–208. 21 indexed citations

May, Philip A., Jason Blankenship, Anna-Susan Marais, et al.. (2013). Maternal alcohol consumption producing fetal alcohol spectrum disorders (FASD): Quantity, frequency, and timing of drinking. Drug and Alcohol Dependence. 133(2). 502–512. 170 indexed citations

Reinstein, Eyal, Ericka Okenfuss, Yael Wilnai, et al.. (2013). Axial spondylometaphyseal dysplasia with retinitis pigmentosa—a clinical report and diagnostic clues. Journal of Applied Genetics. 54(2). 231–234. 1 indexed citations

10.

May, Philip A., Jason Blankenship, Anna‐Susan Marais, et al.. (2012). Approaching the Prevalence of the Full Spectrum of Fetal Alcohol Spectrum Disorders in a South African Population‐Based Study. Alcoholism Clinical and Experimental Research. 37(5). 818–830. 182 indexed citations

11.

May, Philip A., Barbara G. Tabachnick, J. Phillip Gossage, et al.. (2011). Maternal risk factors predicting child physical characteristics and dysmorphology in fetal alcohol syndrome and partial fetal alcohol syndrome. Drug and Alcohol Dependence. 119(1-2). 18–27. 41 indexed citations

12.

Veerapandiyan, Aravindhan, Omar Abdul‐Rahman, Margaret P Adam, et al.. (2011). Chromosome 22q11.2 deletion syndrome in African‐American patients: A diagnostic challenge. American Journal of Medical Genetics Part A. 155(9). 2186–2195. 18 indexed citations

13.

Manning, Melanie & Louanne Hudgins. (2010). Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities. Genetics in Medicine. 12(11). 742–745. 437 indexed citations

14.

May, Philip A., J. Phillip Gossage, Barbara G. Tabachnick, et al.. (2010). Population Differences in Dysmorphic Features Among Children With Fetal Alcohol Spectrum Disorders. Journal of Developmental & Behavioral Pediatrics. 31(4). 304–316. 20 indexed citations

15.

May, Philip A., J. Phillip Gossage, Wendy O. Kalberg, et al.. (2009). Prevalence and epidemiologic characteristics of FASD from various research methods with an emphasis on recent in‐school studies. PubMed. 15(3). 176–192. 641 indexed citations breakdown →

16.

Binenbaum, Gil, Donna M. McDonald‐McGinn, Elaine H. Zackai, et al.. (2008). Sclerocornea associated with the chromosome 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 146A(7). 904–909. 22 indexed citations

17.

Manning, Melanie & Louanne Hudgins. (2007). Use of array-based technology in the practice of medical genetics. Genetics in Medicine. 9(9). 650–653. 24 indexed citations

18.

Enns, Gregory M., A J Barkovich, André B. P. Kuilenburg, et al.. (2004). Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 27(4). 513–522. 17 indexed citations

19.

Morgan, Terry K., Jamie McDonald, Carolyn J. Anderson, et al.. (2002). Intracranial Hemorrhage in Infants and Children With Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome). PEDIATRICS. 109(1). e12–e12. 88 indexed citations

20.

Manning, Melanie & Donald D. Stevenson. (1991). Aspirin sensitivity. Postgraduate Medicine. 90(5). 227–233. 7 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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