Yali Xue

38.7k citations

96 papers · 4.3k indexed · 2 hit papers · h-index 33

Impact in

Genetics top 0.5%
- Forensic and Genetic Research
- Genetic diversity and population structure
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Cancer Research top 5%
- Cancer Genomics and Diagnostics

Papers in

Genetics 61
- Forensic and Genetic Research 23
- Genetic Associations and Epidemiology 18
- Genetic diversity and population structure 15
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
Radiation 6

Co-authors: Chris Tyler‐Smith Marc Haber Massimo Mezzavilla Qasim Ayub Aylwyn Scally Richard Durbin Vagheesh M. Narasimhan Petr Danecek
Journals: The American Journal of Human Genetics (12 papers)Human Genetics (9 papers)Genome biology (5 papers)Forensic Science International Genetics (4 papers)Ceramics International (3 papers)
Partner nations: United Kingdom China United States

In The Last Decade

Yali Xue

93 papers receiving 4.3k citations

Hit Papers

align trajectories log scale

Ancient DNA and the rewriting of human history: be sparing with Occam’s razor 2016 · 796 citations

Peers

Countries citing papers authored by Yali Xue

Since Specialization

Citations

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

Fields of papers citing papers by Yali Xue

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Yali Xue, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yali Xue Line = papers co-authored together Yali Xue links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Design of a narrow-band blue-emitting Rb2Ba3(P2O7)2:Eu2+ phosphor with low thermal quenching for plant growth LEDs Ceramics International ·Yali Xue, Yujun Liang, Qiangke Wang, Weilun Zhang, Yi Dou, Xiaodeng Wu, Yongsheng Han	2023	16
2	Optical tuning and energy transfer of single-phase white-emitting Y3TaO7:Bi3+, Eu3+ for ultraviolet converted pc-WLED with high chromatic stability Journal of Alloys and Compounds ·Yali Xue, Yujun Liang, Yi Dou, Haoran Li, Qiangke Wang, Xiaodeng Wu, Yongsheng Han	2023	16
3	High performance of broad excitation and narrow emission green phosphor NaAl₁₁O₁₇:Eu²⁺, Mn²⁺for backlight displays Journal of Materials Chemistry C ·Yali Xue, Yujun Liang, Weilun Zhang, Yi Dou, Qiangke Wang, Xiaodeng Wu, Yongsheng Han	2023	15
4	A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans eLife ·Pille Hallast, Laura Kibena, Margus Punab, Elena Arciero, Siiri Rootsi, Marina Grigorova, Rodrigo Flores, Mark A. Jobling, Olev Poolamets, Kristjan Pomm, Paul Korrovits, Kristiina Rull, Yali Xue, Chris Tyler‐Smith, Maris Laan	2021	15
5	A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice Molecular Biology and Evolution ·Michał Szpak, Stephan C. Collins, Yan Li, Xiao Liu, Qasim Ayub, Marie‐Christine Fischer, Valerie E. Vancollie, Christopher J. Lelliott, Yali Xue, Binnaz Yalcin, Huanming Yang, Chris Tyler‐Smith	2021	0
6	The genomic history of the Middle East Cell ·Mohamed A. Almarri, Marc Haber, Reem A. Lootah, Pille Hallast, Saeed Al Turki, Hilary C. Martin, Yali Xue, Chris Tyler‐Smith	2021	33
7	The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects The American Journal of Human Genetics ·Hila Fridman, Helger G. Yntema, Reedik Mägi, Reidar Andreson, Andres Metspalu, Massimo Mezzavilla, Chris Tyler‐Smith, Yali Xue, Shai Carmi, Ephrat Levy‐Lahad, Christian Gilissen, Han G. Brunner	2021	34
8	A Transient Pulse of Genetic Admixture from the Crusaders in the Near East Identified from Ancient Genome Sequences The American Journal of Human Genetics ·Marc Haber, Claude Doumet‐Serhal, Christiana L. Scheib, Yali Xue, Richard Mikulski, Rui Martiniano, Bettina Fischer‐Genz, Holger Schutkowski, Toomas Kivisild, Chris Tyler‐Smith	2019	21
9	FineMAV: prioritizing candidate genetic variants driving local adaptations in human populations Genome biology ·Michał Szpak, Massimo Mezzavilla, Qasim Ayub, Yuan Chen, Yali Xue, Chris Tyler‐Smith	2018	15
10	Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits Nature Communications ·Lorraine Southam, Arthur Gilly, Dániel Süveges, Aliki‐Eleni Farmaki, Jeremy Schwartzentruber, Ioanna Tachmazidou, Angela Matchan, Nigel W. Rayner, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini	2017	52
11	Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes Nature Communications ·Vagheesh M. Narasimhan, Raheleh Rahbari, Aylwyn Scally, Arthur Wüster, Dan Mason, Yali Xue, John Wright, Richard C. Trembath, Eamonn R. Maher, David A. van Heel, Adam Auton, Matthew E. Hurles, Chris Tyler‐Smith, Richard Durbin	2017	54
12	A Genome-Wide Survey of Genetic Variation in Gorillas Using Reduced Representation Sequencing PLoS ONE ·Aylwyn Scally, Bryndís Yngvadóttir, Yali Xue, Qasim Ayub, Richard Durbin, Chris Tyler‐Smith	2013	18
13	A calibrated human Y-chromosomal phylogeny based on resequencing Genome Research ·Wei Wei, Qasim Ayub, Yuan Chen, Shane McCarthy, Yiping Hou, Ignazio Carbone, Yali Xue, Chris Tyler‐Smith	2012	92
14	High altitude adaptation in Daghestani populations from the Caucasus Human Genetics ·Luca Pagani, Qasim Ayub, Daniel G. MacArthur, Yali Xue, J. Kenneth Baillie, Yuan Chen, Iwanka Kozarewa, Daniel J. Turner, Sergio Tofanelli, Kazima Bulayeva, Kenneth K. Kídd, Giorgio Paoli, Chris Tyler‐Smith	2011	29
15	A Genome-wide Survey of the Prevalence and Evolutionary Forces Acting on Human Nonsense SNPs The American Journal of Human Genetics ·Bryndís Yngvadóttir, Yali Xue, Steve Searle, Sarah Hunt, Marcos Delgado, Jonathan J. Morrison, Pamela Whittaker, Panos Deloukas, Chris Tyler‐Smith	2009	59
16	Improving global and regional resolution of male lineage differentiation by simple single-copy Y-chromosomal short tandem repeat polymorphisms Forensic Science International Genetics ·Mark Vermeulen, Andreas Wollstein, Kristiaan J. van der Gaag, Óscar Lao, Yali Xue, Qiuju Wang, Lutz Roewer, Hans Knoblauch, Chris Tyler‐Smith, Peter de Knijff, Manfred Kayser	2009	75
17	A Worldwide Survey of Human Male Demographic History Based on Y-SNP and Y-STR Data from the HGDP-CEPH Populations Molecular Biology and Evolution ·Wentao Shi, Qasim Ayub, M. Vermeulen, R.-g. Shao, Silvia Patricia Aquino Zúñiga, Kristiaan J. van der Gaag, Peter de Knijff, Manfred Kayser, Yali Xue, Chris Tyler‐Smith	2009	78
18	Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background Journal of Medical Genetics ·Csilla Krausz, Claudia Giachini, Yali Xue, Moira K. O’Bryan, Jörg Gromoll, Ewa Rajpert‐De Meyts, Rafael Oliva, Isabelle Aknin‐Seifer, E. Erdei, Niels Jørgensen, Manuela Simoni, J. L. Ballescà, Roei Levy, Giancarlo Balercia, Paola Piomboni, Eberhard Nieschlag, Gianni Forti, Robert I. McLachlan, Chris Tyler‐Smith	2008	61
19	Variation of the oxytocin/neurophysin I (OXT) gene in four human populations Journal of Human Genetics ·Yang Xu, Yali Xue, Asan, Allan Daly, Lijie Wu, Chris Tyler‐Smith	2008	6
20	Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y Human Molecular Genetics ·Mark A. Jobling, Iek Chi C. Lo, Daniel J. Turner, Georgina R. Bowden, Andrew C. Lee, Yali Xue, Denise Carvalho‐Silva, Matthew E. Hurles, Susan M. Adams, Yuet Meng Chang, Thirsa Kraaijenbrink, Jürgen Henke, Ginevra Guanti, Brian J. McKeown, Roland A.H. van Oorschot, R. John Mitchell, Peter de Knijff, Chris Tyler‐Smith, Emma J. Parkin	2006	114

About Yali Xue

Yali Xue is a scholar working on Genetics, Radiation, Electronic, Optical and Magnetic Materials, Archeology and Aging, having authored 96 papers that have together received 4.3k indexed citations. Recurring topics across this work include Forensic and Genetic Research (23 papers), Luminescence Properties of Advanced Materials (22 papers), Genetic Associations and Epidemiology (18 papers), Genetic diversity and population structure (15 papers), Crystal Structures and Properties (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Perovskite Materials and Applications (10 papers) and Chromosomal and Genetic Variations (10 papers). The work is most often cited by research in Genetics (2.2k citations), Cancer Research (464 citations), Molecular Biology (2.0k citations), Archeology (266 citations) and Paleontology (117 citations). Yali Xue has collaborated with scholars based in United Kingdom, China and United States. Frequent co-authors include Chris Tyler‐Smith, Marc Haber, Massimo Mezzavilla, Qasim Ayub, Aylwyn Scally, Richard Durbin, Vagheesh M. Narasimhan, Petr Danecek, Yuan Chen and Dan Zhao. Their work appears in journals such as The American Journal of Human Genetics, Human Genetics, Genome biology, Forensic Science International Genetics and Ceramics International.

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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