Francisca Millan

3.3k total citations
19 papers, 479 citations indexed

About

Francisca Millan is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Francisca Millan has authored 19 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Psychiatry and Mental health. Recurrent topics in Francisca Millan's work include Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Francisca Millan is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (5 papers). Francisca Millan collaborates with scholars based in United States, Canada and Qatar. Francisca Millan's co-authors include Kyle Retterer, Elaine H. Zackai, Holly Dubbs, Wendy K. Chung, Megan T. Cho, Kenneth N. Rosenbaum, Ann Nordgren, Helena Malmgren, Golder N. Wilson and Michael Parker and has published in prestigious journals such as JAMA, Nature Communications and Neurology.

In The Last Decade

Francisca Millan

16 papers receiving 470 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francisca Millan United States 11 261 250 50 49 35 19 479
Krystyna Szymańska Poland 14 218 0.8× 177 0.7× 52 1.0× 38 0.8× 23 0.7× 48 485
Marcello Scala Italy 15 207 0.8× 178 0.7× 91 1.8× 37 0.8× 16 0.5× 61 513
Sanne M. C. Savelberg Netherlands 10 246 0.9× 257 1.0× 38 0.8× 31 0.6× 14 0.4× 11 443
Tarja Linnankivi Finland 14 424 1.6× 142 0.6× 29 0.6× 43 0.9× 37 1.1× 22 631
Michelle Demos Canada 13 270 1.0× 145 0.6× 64 1.3× 31 0.6× 16 0.5× 23 482
Tatjana Bierhals Germany 13 271 1.0× 201 0.8× 18 0.4× 55 1.1× 13 0.4× 26 446
Kelly D. Farwell Hagman United States 12 218 0.8× 475 1.9× 85 1.7× 53 1.1× 11 0.3× 20 630
Sébastien Chénier Canada 11 261 1.0× 278 1.1× 17 0.3× 34 0.7× 15 0.4× 17 473
Renske Oegema Netherlands 13 245 0.9× 217 0.9× 23 0.5× 147 3.0× 16 0.5× 21 534
Takuya Hiraide Japan 12 271 1.0× 185 0.7× 26 0.5× 26 0.5× 17 0.5× 34 441

Countries citing papers authored by Francisca Millan

Since Specialization
Citations

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

Fields of papers citing papers by Francisca Millan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francisca Millan

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

All Works

19 of 19 papers shown
1.
Torene, Rebecca I., María J. Guillen Sacoto, Francisca Millan, et al.. (2023). Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases. The American Journal of Human Genetics. 111(1). 70–81. 10 indexed citations
2.
Lines, Matthew A., Alexanne Cuillerier, Pranesh Chakraborty, et al.. (2021). A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency. European Journal of Human Genetics. 29(11). 1719–1724. 4 indexed citations
3.
Webb, Bryn D., Thomas P. Naidich, Lynne M. Bird, et al.. (2021). Haploinsufficiency of POU4F1 causes an ataxia syndrome with hypotonia and intention tremor. Human Mutation. 42(6). 685–693.
4.
Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. JAMA. 325(5). 467–467. 71 indexed citations
5.
Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. Obstetrical & Gynecological Survey. 76(7). 399–401.
6.
Yoon, Grace, Graeme Nimmo, Christopher M. Gómez, et al.. (2020). De Novo variants in EEF2 cause a neurodevelopmental disorder with benign external hydrocephalus. Human Molecular Genetics. 29(24). 3892–3899. 10 indexed citations
7.
8.
Millan, Francisca, et al.. (2019). Genetic testing of >1300 patients with cerebral palsy reveals an etiology in one-third of cases, underscoring the need for broad genetic testing and a significant recurrence risk for families. (P4.6-028). 92. 1 indexed citations
9.
Rabin, Rachel, Francisca Millan, Juan Cabrera‐Luque, & John Pappas. (2018). Intellectual disability due to monoallelic variant in GATAD2B and mosaicism in unaffected parent. American Journal of Medical Genetics Part A. 176(12). 2907–2910. 6 indexed citations
10.
Huppke, Peter, Susann Weißbach, Joseph A. Church, et al.. (2017). Activating de novo mutations in NFE2L2 encoding NRF2 cause a multisystem disorder. Nature Communications. 8(1). 818–818. 64 indexed citations
11.
Zárate, Yuri A., Louisa Kalsner, Alice Basinger, et al.. (2017). Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome. Clinical Genetics. 92(4). 423–429. 28 indexed citations
12.
Millan, Francisca, Dianalee McKnight, Julie Scuffins, et al.. (2017). EXOME SEQUENCING OFFERS A COMPREHENSIVE GENETIC EVALUATION AND HIGH DIAGNOSTIC RATE FOR ATAXIA-RELATED DISORDERS (S17.004). Neurology. 88(16_supplement).
13.
Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations
14.
Millan, Francisca, Megan T. Cho, Kyle Retterer, et al.. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American Journal of Medical Genetics Part A. 170(7). 1791–1798. 42 indexed citations
15.
Retterer, Kyle, Francisca Millan, C. Nowak, et al.. (2016). De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females. Clinical Genetics. 91(5). 756–763. 22 indexed citations
16.
Berko, Esther R., Megan T. Cho, Christine M. Eng, et al.. (2016). De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. Journal of Medical Genetics. 54(2). 84–86. 44 indexed citations
17.
Ye, Yizhou, Megan T. Cho, Kyle Retterer, et al.. (2015). De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly. Molecular Case Studies. 1(1). a000455–a000455. 39 indexed citations
18.
Tham, Emma, Anna Lindstrand, Avni Santani, et al.. (2015). Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features. The American Journal of Human Genetics. 96(3). 507–513. 87 indexed citations
19.
Zárate, Yuri A., Julie R. Jones, Melanie A. Jones, et al.. (2015). Lessons from a pair of siblings with BPAN. European Journal of Human Genetics. 24(7). 1080–1083. 25 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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