Mark E. Nuñes

1.2k total citations
24 papers, 644 citations indexed

About

Mark E. Nuñes is a scholar working on Genetics, Molecular Biology and Developmental Biology. According to data from OpenAlex, Mark E. Nuñes has authored 24 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Developmental Biology. Recurrent topics in Mark E. Nuñes's work include Congenital limb and hand anomalies (5 papers), Alkaline Phosphatase Research Studies (4 papers) and Genomics and Rare Diseases (3 papers). Mark E. Nuñes is often cited by papers focused on Congenital limb and hand anomalies (5 papers), Alkaline Phosphatase Research Studies (4 papers) and Genomics and Rare Diseases (3 papers). Mark E. Nuñes collaborates with scholars based in United States, France and Germany. Mark E. Nuñes's co-authors include Peter H. Byers, Anne-Sophie Lia-Baldini, Melanie Pepin, Deborah Krakow, Brigitte Simon‐Bouy, Étienne Mornet, Isabelle Brun‐Heath, Frederick W. Luthardt, Mary K. Kukolich and Raj P. Kapur and has published in prestigious journals such as Human Molecular Genetics, American Journal of Obstetrics and Gynecology and British Journal of Haematology.

In The Last Decade

Mark E. Nuñes

24 papers receiving 628 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark E. Nuñes United States 12 237 211 202 183 95 24 644
Taichi Kitaoka Japan 16 254 1.1× 349 1.7× 273 1.4× 201 1.1× 18 0.2× 49 798
B. Leheup France 11 85 0.4× 105 0.5× 126 0.6× 37 0.2× 7 0.1× 29 372
Mariana F.A. Funari Brazil 17 232 1.0× 400 1.9× 368 1.8× 23 0.1× 15 0.2× 35 736
Takeki Hirano Japan 14 221 0.9× 238 1.1× 170 0.8× 13 0.1× 13 0.1× 28 549
Kanshi Minamitani Japan 15 316 1.3× 186 0.9× 188 0.9× 78 0.4× 42 678
Hiromichi Ikawa Japan 17 27 0.1× 133 0.6× 196 1.0× 123 0.7× 3 0.0× 45 770
S.K. Abbas United Kingdom 11 62 0.3× 107 0.5× 259 1.3× 46 0.3× 2 0.0× 22 576
Weiwei Hu China 12 32 0.1× 166 0.8× 148 0.7× 163 0.9× 2 0.0× 21 463
Cristina Tau Argentina 10 57 0.2× 99 0.5× 151 0.7× 87 0.5× 16 505
McKusick Va United States 17 25 0.1× 254 1.2× 166 0.8× 70 0.4× 8 0.1× 61 809

Countries citing papers authored by Mark E. Nuñes

Since Specialization
Citations

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

Fields of papers citing papers by Mark E. Nuñes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark E. Nuñes. 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 Mark E. Nuñes. The network helps show where Mark E. Nuñes may publish in the future.

Co-authorship network of co-authors of Mark E. Nuñes

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

All Works

20 of 20 papers shown
1.
Freeman, Rebecca, Adriana Backx Noronha Viana, Jason Carmichael, et al.. (2024). Applying data science methodologies with artificial intelligence variant reinterpretation to map and estimate genetic disorder prevalence utilizing clinical data. American Journal of Medical Genetics Part A. 194(5). e63505–e63505. 5 indexed citations
2.
Kishnani, Priya S., Eric T. Rush, Paul Arundel, et al.. (2017). Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa. Molecular Genetics and Metabolism. 122(1-2). 4–17. 96 indexed citations
3.
Allyse, Megan, Umut Aypar, Natasha Bonhomme, et al.. (2017). Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. Journal of Women s Health. 26(7). 755–761. 9 indexed citations
4.
Hagman, Kelly D. Farwell, Deepali N. Shinde, Cameron Mroske, et al.. (2016). Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine. 19(2). 224–235. 34 indexed citations
5.
Pretorius, Dolores H., Abraham Rothman, Mark E. Nuñes, et al.. (2012). Improved Prenatal Detection of Congenital Heart Disease in an Integrated Health Care System. Pediatric Cardiology. 34(3). 670–679. 61 indexed citations
6.
Lia-Baldini, Anne-Sophie, Isabelle Brun‐Heath, Claire Carrion, et al.. (2008). A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein. Human Genetics. 123(4). 429–432. 38 indexed citations
7.
Nuñes, Mark E., et al.. (2008). Desmopressin responsiveness in children with Ehlers‐Danlos syndrome associated bleeding symptoms. British Journal of Haematology. 144(2). 230–233. 30 indexed citations
8.
Brun‐Heath, Isabelle, Anne-Sophie Lia-Baldini, Stéphane Maillard, et al.. (2007). Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasia. European Journal of Medical Genetics. 50(5). 367–378. 29 indexed citations
9.
Byers, Peter H., Deborah Krakow, Mark E. Nuñes, & Melanie Pepin. (2006). Genetic evaluation of suspected osteogenesis imperfecta (OI). Genetics in Medicine. 8(6). 383–388. 57 indexed citations
10.
Fries, Melissa H., Michael T. Bashford, & Mark E. Nuñes. (2005). Implementing prenatal screening for cystic fibrosis in routine obstetric practice. American Journal of Obstetrics and Gynecology. 192(2). 527–534. 9 indexed citations
11.
12.
Lia-Baldini, Anne-Sophie, Françoise Müller, A. Taillandier, et al.. (2001). A molecular approach to dominance in hypophosphatasia. Human Genetics. 109(1). 99–108. 88 indexed citations
13.
Seto, Marianne L., Mark E. Nuñes, Craig A. MacArthur, & Michael L. Cunningham. (1997). Pathogenesis of ectrodactyly in theDactylaplasia mouse: Aberrant cell death of the apical ectodermal ridge. Teratology. 56(4). 262–270. 21 indexed citations
14.
Tar, Attila, Alexandra Ion, J. Sólyom, et al.. (1997). Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13. American Journal of Medical Genetics. 68(2). 231–235. 7 indexed citations
15.
Tsipouras, Petros, Fiorella Gurrieri, Panagiotis Prinos, et al.. (1996). A split hand-split foot (SHFM3) gene is located at 10Q24→25. American Journal of Medical Genetics. 62(4). 427–436. 46 indexed citations
16.
Nuñes, Mark E., et al.. (1996). Swine cytosolic malic enzyme: cDNA cloning, sequencing, and localization. Mammalian Genome. 7(11). 815–821. 10 indexed citations
17.
Chardon, P., et al.. (1995). Dinucleotide repeat polymorphism at the porcine TNFA locus. Animal Genetics. 26(5). 366–367. 2 indexed citations
18.
Nuñes, Mark E., Raj P. Kapur, Frederick W. Luthardt, et al.. (1995). A second autosomal split hand/split foot locus maps to chromosome 10q24-q25. Human Molecular Genetics. 4(11). 2165–2170. 60 indexed citations
19.
Nuñes, Mark E., et al.. (1994). Characterization of six new loci within the swine major histocompatibility complex class III region. Mammalian Genome. 5(10). 616–622. 13 indexed citations
20.
Nuñes, Mark E., et al.. (1987). c-myc expression in the thyroid. I: Normal, adenomatous, and cancerous thyroid tissue.. PubMed. 17. 63–5. 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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