ArticleNPJ genomic medicine2016
Genome-wide characteristics of
Open access · goldAbstract read
In one paragraph
Article in NPJ genomic medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 1 pooled it
34.5field-weighted citation impact, top 1% of its field
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
130 citing papers in PubMed, 1 synthesis or guideline pooled it, 237 citations in OpenAlex.
- Fertility in the aging male: a systematic review.Fertility and sterility · 2022Pooled it
- Sexual dimorphism of autism-like phenotypes in microglial eIF4E overexpression mice.bioRxiv : the preprint server for biology · 2026Article
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- Genetic alterations in SUPT6H are associated with neurodevelopmental disorders.Biochimica et biophysica acta. Molecular basis of disease · 2026Article
- Identification of a Novel De Novo Heterozygous SEC61A1 Variant in a Patient With Severe Congenital Neutropenia.Molecular genetics & genomic medicine · 2026Article
- Autism spectrum disorder trios from consanguineous populations are enriched for rare homozygous variants, identifying 32 new candidate genes.Scientific reports · 2026Article
- Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis.Human genetics · 2026Article
- Genomic landscape of autism spectrum disorder in Brazil.Genetics and molecular biology · 2026Article
- Inherent instability of simple DNA repeats shapes an evolutionarily stable distribution of repeat lengths.Nature communications · 2025Article
- Exploring the Association Between Medically Assisted Reproduction and Autism Spectrum Disorder: Clinical Correlations from a Retrospective Cohort.Pediatric reports · 2025Article
- NoncodingiScience · 2025Article
- A signal transduction blind spot: the function of adenylyl cyclase transmembrane domains.The FEBS journal · 2025Review
- Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders.Genome medicine · 2025Article
- Persistent cortical excitatory neuron dysregulation in adultResearch square · 2025Article
- Advancing precision diagnosis in autism: Insights from large-scale genomic studies.Molecules and cells · 2025Review
- Decoding the genetic landscape of autism: A comprehensive review.World journal of clinical pediatrics · 2024Article
- Low-level brain somatic mutations in exonic regions are collectively implicated in autism with germline mutations in autism risk genes.Experimental & molecular medicine · 2024Article
- The Importance of Large-Scale Genomic Studies to Unravel Genetic Risk Factors for Autism.International journal of molecular sciences · 2024Review
- Proteome-Wide Assessment of Clustering of Missense Variants in Neurodevelopmental Disorders Versus Cancer.medRxiv : the preprint server for health sciences · 2024Article
- Article
70 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
48 authors at 9 institutions in 4 countries.
Ryan K C YuenThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Daniele MericoThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Hongzhi CaoBGI-Shenzhen, Yantian, Shenzhen, China.
Giovanna PellecchiaThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Babak AlipanahiDepartment of Electrical and Computer Engineering, University of Toronto, Toronto, Ontario, Canada.
Bhooma ThiruvahindrapuramThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Xin TongBGI-Shenzhen, Yantian, Shenzhen, China.
Yuhui SunBGI-Shenzhen, Yantian, Shenzhen, China.
Dandan CaoBGI-Shenzhen, Yantian, Shenzhen, China.
Tao ZhangBGI-Shenzhen, Yantian, Shenzhen, China.
Xueli WuBGI-Shenzhen, Yantian, Shenzhen, China.
Xin JinBGI-Shenzhen, Yantian, Shenzhen, China.
Ze ZhouBGI-Shenzhen, Yantian, Shenzhen, China.
Xiaomin LiuBGI-Shenzhen, Yantian, Shenzhen, China.
Thomas NalpathamkalamThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Susan WalkerThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Jennifer L HoweThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Zhuozhi WangThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Jeffrey R MacDonaldThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Ada ChanThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Lia D'AbateThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Eric DeneaultThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Michelle T SiuProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Kristiina TammimiesCenter of Neurodevelopmental Disorders (KIND), Pediatric Neuropsychiatry Unit, Karolinska Institutet, Stockholm, Sweden.
Mohammed UddinThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Mehdi ZarreiThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Mingbang WangBGI-Shenzhen, Yantian, Shenzhen, China.
Yingrui LiBGI-Shenzhen, Yantian, Shenzhen, China.
Jun WangBGI-Shenzhen, Yantian, Shenzhen, China.
Jian WangBGI-Shenzhen, Yantian, Shenzhen, China.
Huanming YangBGI-Shenzhen, Yantian, Shenzhen, China.
Matt BookmanGoogle, Mountain View, California, USA.
Jonathan BinghamGoogle, Mountain View, California, USA.
Samuel S GrossGoogle, Mountain View, California, USA.
Dion LoyGoogle, Mountain View, California, USA.
Mathew PletcherAutism Speaks, Princeton, New Jersey, USA.
Christian R MarshallThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Molecular Genetics, Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Evdokia AnagnostouBloorview Research Institute, University of Toronto, Toronto, Ontario, Canada.
Lonnie ZwaigenbaumDepartment of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
Rosanna WeksbergProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Bridget A FernandezDisciplines of Genetics and Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada; Provincial Medical Genetic Program, Eastern Health, St. John's, Newfoundland, Canada.
Wendy RobertsAutism Research Unit, The Hospital for Sick Children, Toronto, Ontario, Canada.
Peter SzatmariAutism Research Unit, The Hospital for Sick Children, Toronto, Ontario, Canada; Child Youth and Family Services, Centre for Addiction and Mental Health, Toronto, Ontario, Canada; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
David GlazerProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Brendan J FreyDepartment of Electrical and Computer Engineering, University of Toronto, Toronto, Ontario, Canada; Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada.
Robert H RingAutism Speaks, Princeton, New Jersey, USA.
Xun XuBGI-Shenzhen, Yantian, Shenzhen, China.
Stephen W SchererThe Centre for Applied Genomics, Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada; McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada.
Hospital for Sick Children · CABGI Group (China) · CNGoogle (United States) · USUniversity of Toronto · CAAutism Speaks · USHolland Bloorview Kids Rehabilitation Hospital · CAKarolinska Institutet · SEMemorial University of Newfoundland · CAUniversity of Alberta · CA
Funding
CIHR 140849-1PHS HHS 140849-1
Abstract
PubMed holds no abstract for this paper.
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What OpenQuestion holds
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LicenceCC BY
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.