Francesco Vallania

3.5k citations

32 papers · 1.9k indexed · h-index 21

Co-authors: Purvesh Khatri Robi D. Mitra Winston Haynes Mark M. Davis Paul J. Utz Steven Schaffert Todd E. Druley Timothy E. Sweeney
Topics: Genomics and Rare Diseases (7 papers)Single-cell and spatial transcriptomics (5 papers)Cancer Genomics and Diagnostics (5 papers)
Cited by: Aging Immunology Genetics
Journals: Nature Cell Proceedings of the National Academy of Sciences
Partner nations: United States China Italy

In The Last Decade

Francesco Vallania

32 papers receiving 1.9k citations

Peers

Countries citing papers authored by Francesco Vallania

Since Specialization

Citations

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

Fields of papers citing papers by Francesco Vallania

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesco Vallania

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

#	Work	Indexed citations
1	Multicohort Analysis Identifies Monocyte Gene Signatures to Accurately Monitor Subset-Specific Changes in Human Diseases 2021 ·Frontiers in Immunology ·Francesco Vallania,(unknown),Claudia Macaubas,Shu-Chen Hung,Narendiran Rajasekaran,(unknown),Jonathan Graf,Mary C. Nakamura,Elizabeth Mellins,Purvesh Khatri	8
2	Cellular senescence impairs the reversibility of pulmonary arterial hypertension 2020 ·Science Translational Medicine ·Diederik E. van der Feen,Guido P. L. Bossers,Quint A. J. Hagdorn,Jan-Renier Moonen,Kondababu Kurakula,Robert Szulcek,James Chappell,Francesco Vallania,Michele Donato,Klaas Kok,Jaskaren Kohli,Arjen H. Petersen,(unknown),Marco Demaria,Marie‐José Goumans,Rudolf A. de Boer,Purvesh Khatri,Marlene Rabinovitch,Rolf M.F. Berger,Beatrijs Bartelds	85
3	Leveraging heterogeneity across multiple datasets increases cell-mixture deconvolution accuracy and reduces biological and technical biases 2018 ·Nature Communications ·Francesco Vallania,Andrew Tam,Shane Lofgren,Steven Schaffert,Tej D. Azad,Erika Bongen,Winston Haynes,(unknown),Michael N. Alonso,Mark M. Davis,Edgar G. Engleman,Purvesh Khatri	100
4	Interpretation of biological experiments changes with evolution of the Gene Ontology and its annotations 2018 ·Scientific Reports ·Aurelie Tomczak,Jonathan Mortensen,Rainer Winnenburg,Charles Y. Liu,(unknown),(unknown),Francesco Vallania,Shane Lofgren,Winston Haynes,Nigam H. Shah,Mark A. Musen,Purvesh Khatri	98
5	Single-cell epigenetics – Chromatin modification atlas unveiled by mass cytometry 2018 ·Clinical Immunology ·Peggie Cheung,Francesco Vallania,Mai Dvorak,Sarah E. Chang,Steven Schaffert,Michele Donato,Aditya Rao,Rong Mao,Paul J. Utz,Purvesh Khatri,Alex Kuo	24
6	KLRD1-expressing natural killer cells predict influenza susceptibility 2018 ·Genome Medicine ·Erika Bongen,Francesco Vallania,Paul J. Utz,Purvesh Khatri	42
7	A multi-cohort study of the immune factors associated with M. tuberculosis infection outcomes 2018 ·Nature ·Roshni Roy Chowdhury,Francesco Vallania,Qianting Yang,Cesar J. Lopez Angel,Fatoumatta Darboe,Adam Penn‐Nicholson,Virginie Rozot,Elisa Nemes,Stephanus T. Malherbe,Katharina Ronacher,Gerhard Walzl,Willem A. Hanekom,Mark M. Davis,Jill Winter,Xinchun Chen,Thomas J. Scriba,Purvesh Khatri,Yueh‐hsiu Chien	156
8	Validating single-cell genomics for the study of renal development 2014 ·Kidney International ·Sanjay Jain,Michiel J. Noordam,Masato Hoshi,Francesco Vallania,Donald F. Conrad	2
9	Origin and Consequences of the Relationship between Protein Mean and Variance 2014 ·PLoS ONE ·Francesco Vallania,Marc S. Sherman,(unknown),Ilaria Mogno,Barak A. Cohen,Robi D. Mitra	11
10	Performance of Common Analysis Methods for Detecting Low-Frequency Single Nucleotide Variants in Targeted Next-Generation Sequence Data 2013 ·Journal of Molecular Diagnostics ·David H. Spencer,Manoj Tyagi,Francesco Vallania,Andrew J. Bredemeyer,John D. Pfeifer,Robi D. Mitra,Eric J. Duncavage	84
11	Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families 2012 ·PLoS ONE ·Carlos Cruchaga,Sumitra Chakraverty,Kevin H. Mayo,Francesco Vallania,Robi D. Mitra,Kelley Faber,Jennifer Williamson,T. Bird,Ramon Diaz‐Arrastia,Tatiana Foroud,Bradley F. Boeve,Neill R. Graff‐Radford,Pamela St. Jean,Michael J. Lawson,Margaret G. Ehm,Richard Mayeux,Alison Goate	206
12	Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing 2012 ·BMC Genomics ·Enrique Ramos,(unknown),Sara E. Chasnoff,Andrew Hughes,Andrew L. Young,Katherine A. Thornton,(unknown),Francesco Vallania,(unknown),Todd E. Druley	18
13	Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families 2012 ·PLoS ONE ·Carlos Cruchaga,Sumitra Chakraverty,Kevin H. Mayo,Francesco Vallania,Robi D. Mitra,Kelley Faber,Jennifer Williamson,Thomas G. Bird,Ramon Diaz‐Arrastia,Tatiana Foroud,Bradley F. Boeve,Neill R. Graff‐Radford,Pamela St. Jean,Michael J. Lawson,Margaret G. Ehm,Richard Mayeux,Alison Goate	30
14	Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER 2012 ·Journal of Visualized Experiments ·Francesco Vallania,(unknown),Sharon Cresci,Robi D. Mitra,Todd E. Druley	2
15	Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER 2012 ·Journal of Visualized Experiments ·Francesco Vallania,Enrique Ramos,Sharon Cresci,Robi D. Mitra,Todd E. Druley	7
16	Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence 2011 ·Human Molecular Genetics ·Gabe Haller,Todd E. Druley,Francesco Vallania,Robi D. Mitra,Ping Li,Gustav Akk,Joe Henry Steinbach,Naomi Breslau,Eric O. Johnson,Dorothy K. Hatsukami,Jerry A. Stitzel,Laura J. Bierut,Alison Goate	43
17	TATA is a modular component of synthetic promoters 2010 ·Genome Research ·Ilaria Mogno,Francesco Vallania,Robi D. Mitra,Barak A. Cohen	77
18	High-throughput discovery of rare insertions and deletions in large cohorts 2010 ·Genome Research ·Francesco Vallania,Todd E. Druley,Enrique Ramos,Jue Wang,(unknown),(unknown),Robi D. Mitra	43
19	Quantification of rare allelic variants from pooled genomic DNA 2009 ·Nature Methods ·Todd E. Druley,Francesco Vallania,Daniel Wegner,Katherine E. Varley,(unknown),Jacqueline A. Bonds,Sarah W. Robison,Scott W Doniger,Aaron Hamvas,F. Sessions Cole,Justin C. Fay,Robi D. Mitra	125
20	Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease 2009 ·Journal of Clinical Investigation ·Scot J. Matkovich,Derek J. Van Booven,Anna Hindes,Min Young Kang,Todd E. Druley,Francesco Vallania,Robi D. Mitra,Muredach P. Reilly,Thomas P. Cappola,Gerald W. Dorn	44

About Francesco Vallania

Francesco Vallania is a scholar working on Immunology, Genetics and Cancer Research, having authored 32 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Single-cell and spatial transcriptomics (5 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Aging (38 citations), Immunology (427 citations) and Genetics (428 citations). Francesco Vallania has collaborated with scholars based in United States, China and Italy. Frequent co-authors include Purvesh Khatri, Robi D. Mitra, Winston Haynes, Mark M. Davis, Paul J. Utz, Steven Schaffert, Todd E. Druley, Timothy E. Sweeney, Michele Donato and Erika Bongen. Their work appears in journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

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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