Outputs for Harvard University

1 July 2019 - 30 June 2020

United States of America (USA)

Region: Global

Sector: All

Subject/journal group: All

Count Share
2567 923.48

The research outputs below are grouped by journal. Click on the journal to view the list of articles.

Journal Count Share
ACS Nano 23 8.37
Advanced Functional Materials 21 7.54
Advanced Materials 21 5.81
American Journal of Human Genetics 46 6.36
Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data.
2020-06-04
0.06
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy.
2020-06-04
0.07
Polymorphic Inversions Underlie the Shared Genetic Susceptibility of Obesity-Related Diseases.
2020-06-04
0.05
Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental Anomalies Due to Abnormal Hedgehog Signaling.
2020-05-12
0.02
Pleiotropy-Based Decomposition of Genetic Risk Scores: Association and Interaction Analysis for Type 2 Diabetes and CAD.
2020-04-14
0.93
Genotyping Array Design and Data Quality Control in the Million Veteran Program.
2020-04-02
0.04
Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy.
2020-03-26
0.05
Incidence, Origin, and Predictive Model for the Detection and Clinical Management of Segmental Aneuploidies in Human Embryos.
2020-03-19
0.01
Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures.
2020-03-18
0.03
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.
2020-03-16
0.10
Population Histories of the United States Revealed through Fine-Scale Migration and Haplotype Analysis.
2020-03-05
0.13
Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders.
2020-02-25
0.02
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
2020-01-23
0.01
Allele-Specific QTL Fine Mapping with PLASMA.
2020-01-22
0.79
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency.
2020-01-03
0.02
Pathogenic Bi-Allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency.
2019-12-18
0.02
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
2019-12-16
0.08
SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility.
2019-12-13
0.55
UK Biobank Whole-Exome Sequence Binary Phenome Analysis with Robust Region-based Rare-Variant Test.
2019-12-13
0.11
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.
2019-11-12
0.04
A Fast and Accurate Method for Genome-Wide Scale Phenome-Wide G × E Analysis and Its Application to UK Biobank.
2019-11-05
0.06
CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations.
2019-10-31
0.52
Multivariate Genome-Wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy.
2019-10-30
0.04
Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.
2019-10-29
0.04
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder.
2019-10-23
0.09
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.
2019-10-21
0.32
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
2019-10-21
0.10
Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population.
2019-10-03
0.09
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects.
2019-10-03
0.09
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype.
2019-10-03
0.06
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.
2019-09-26
0.07
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.
2019-09-24
0.01
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
2019-09-24
0.08
GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.
2019-09-18
0.05
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies.
2019-09-18
0.14
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype.
2019-08-26
0.06
Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.
2019-08-16
0.03
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
2019-08-13
0.06
Pathogenic Abnormal Splicing due to Intronic Deletions that Induce Biophysical Space Constraint for Spliceosome Assembly.
2019-08-09
0.08
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.
2019-08-08
0.17
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation.
2019-08-05
0.05
Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.
2019-08-01
0.01
Extreme Polygenicity of Complex Traits Is Explained by Negative Selection
2019-07-29
0.88
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.
2019-07-16
0.07
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia.
2019-07-11
0.07
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.
2019-07-02
0.02
Analytical Chemistry 10 3.27
Angewandte Chemie International Edition 26 11.42
Applied Physics Letters 3 1.24
Astronomy & Astrophysics 1 0.03
Cancer Cell 19 10.42
Cancer Research 34 10.75
Cell 63 25.12
Cell Host & Microbe 20 7.30
Cell Metabolism 18 5.97
Cell Stem Cell 23 7.99
Chemical Communications 13 6.36
Chemical Science 13 4.58
Current Biology 27 12.44
Developmental Cell 13 8.34
Earth and Planetary Science Letters 13 4.98
Environmental Science and Technology 28 7.63
European Physical Journal C 22 0.61
Genes & Development 10 4.09
Genome Research 11 3.76
Geochimica et Cosmochimica Acta 9 2.99
Geology 2 0.58
Geophysical Research Letters 38 9.50
Immunity 16 4.38
Inorganic Chemistry 3 0.69
Journal of Biological Chemistry 35 19.73
Journal of Cell Biology 11 4.52
Journal of Clinical Investigation 50 18.18
Journal of Experimental Medicine 12 4.12
Journal of Geophysical Research: Atmospheres 20 3.76
Journal of Geophysical Research: Solid Earth 1 0.10
Journal of High Energy Physics 65 22.99
Journal of Neuroscience 37 17
Journal of the American Chemical Society 39 23.74
Molecular Cell 34 15.78
Molecular Psychiatry 47 7.63
Monthly Notices of the Royal Astronomical Society: Letters 6 0.93
Nano Letters 35 11.89
Nature 136 48.09
Nature Biotechnology 32 15
Nature Cell Biology 13 6.85
Nature Chemical Biology 14 8.39
Nature Chemistry 4 1.02
Nature Climate Change 1 0.02
Nature Communications 337 100.01
Nature Genetics 42 10.54
Nature Geoscience 5 1.37
Nature Immunology 17 6.50
Nature Materials 6 2.72
Nature Medicine 52 16.34
Nature Methods 15 5.68
Nature Nanotechnology 6 1.62
Nature Neuroscience 25 7.07
Nature Photonics 2 0.83
Nature Physics 12 5.39
Nature Structural & Molecular Biology 5 1.15
Neuron 31 12.18
Organic Letters 3 0.58
PLOS Biology 17 4.42
PLOS Genetics 22 5.89
Physical Review A 11 2.69
Physical Review B 18 9.34
Physical Review D 6 3.94
Physical Review Letters 68 29.18
Physical Review X 21 9.68
Proceedings of the National Academy of Sciences of the United States of America 243 107.52
Proceedings of the Royal Society B 13 4.57
Science 88 33.61
Science Advances 92 31.53
Science Translational Medicine 44 13.82
The Astrophysical Journal Letters 101 19.43
The EMBO Journal 3 1.42
The ISME Journal: Multidisciplinary Journal of Microbial Ecology 4 0.87
The Journal of Physical Chemistry Letters 2 1.60
eLife 118 59.70

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