Harvard Catalyst Profiles

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Christoph Lange, Ph.D.

Co-Author

This page shows the publications co-authored by Christoph Lange and Sharon Lutz.
Connection Strength

5.171
  1. Caution against examining the role of reverse causality in Mendelian Randomization. Genet Epidemiol. 2021 Jul; 45(5):445-454.
    View in: PubMed
    Score: 0.978
  2. The effects of misspecification of the mediator and outcome in mediation analysis. Genet Epidemiol. 2020 06; 44(4):400-403.
    View in: PubMed
    Score: 0.901
  3. A general approach to testing for pleiotropy with rare and common variants. Genet Epidemiol. 2017 Feb; 41(2):163-170.
    View in: PubMed
    Score: 0.718
  4. An alternative hypothesis testing strategy for secondary phenotype data in case-control genetic association studies. Front Genet. 2014; 5:188.
    View in: PubMed
    Score: 0.607
  5. Testing for direct genetic effects using a screening step in family-based association studies. Front Genet. 2013; 4:243.
    View in: PubMed
    Score: 0.582
  6. A general semi-parametric approach to the analysis of genetic association studies in population-based designs. BMC Genet. 2013 Feb 28; 14:13.
    View in: PubMed
    Score: 0.553
  7. Genome-wide association analysis of COVID-19 mortality risk in SARS-CoV-2 genomes identifies mutation in the SARS-CoV-2 spike protein that colocalizes with P.1 of the Brazilian strain. Genet Epidemiol. 2021 Jun 22.
    View in: PubMed
    Score: 0.246
  8. A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. BMC Genet. 2015 Dec 03; 16:138.
    View in: PubMed
    Score: 0.167
  9. On the adjustment for covariates in genetic association analysis: a novel, simple principle to infer direct causal effects. Genet Epidemiol. 2009 Jul; 33(5):394-405.
    View in: PubMed
    Score: 0.107
  10. locStra: Fast analysis of regional/global stratification in whole-genome sequencing studies. Genet Epidemiol. 2021 Feb; 45(1):82-98.
    View in: PubMed
    Score: 0.058
  11. Genetic Advances in Chronic Obstructive Pulmonary Disease. Insights from COPDGene. Am J Respir Crit Care Med. 2019 09 15; 200(6):677-690.
    View in: PubMed
    Score: 0.054
  12. Gene-based segregation method for identifying rare variants in family-based sequencing studies. Genet Epidemiol. 2017 05; 41(4):309-319.
    View in: PubMed
    Score: 0.045
  13. Integrating Multiple Correlated Phenotypes for Genetic Association Analysis by Maximizing Heritability. Hum Hered. 2015; 79(2):93-104.
    View in: PubMed
    Score: 0.041
  14. Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease. Am J Respir Cell Mol Biol. 2014 Nov; 51(5):678-87.
    View in: PubMed
    Score: 0.039
  15. Quantitative computed tomography measures of pectoralis muscle area and disease severity in chronic obstructive pulmonary disease. A cross-sectional study. Ann Am Thorac Soc. 2014 Mar; 11(3):326-34.
    View in: PubMed
    Score: 0.037
  16. Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis. Lancet Respir Med. 2014 Mar; 2(3):214-25.
    View in: PubMed
    Score: 0.037
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.