Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Christoph Lange, Ph.D.

Co-Author

This page shows the publications co-authored by Christoph Lange and Julian Hecker.
Connection Strength

5.626
  1. A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests. Bioinformatics. 2020 Dec 26.
    View in: PubMed
    Score: 0.912
  2. A flexible and nearly optimal sequential testing approach to randomized testing: QUICK-STOP. Genet Epidemiol. 2020 03; 44(2):139-147.
    View in: PubMed
    Score: 0.844
  3. A comparison of popular TDT-generalizations for family-based association analysis. Genet Epidemiol. 2019 04; 43(3):300-317.
    View in: PubMed
    Score: 0.795
  4. Family-based tests for associating haplotypes with general phenotype data: Improving the FBAT-haplotype algorithm. Genet Epidemiol. 2018 02; 42(1):123-126.
    View in: PubMed
    Score: 0.736
  5. Reporting Correct p Values in VEGAS Analyses. Twin Res Hum Genet. 2017 06; 20(3):257-259.
    View in: PubMed
    Score: 0.703
  6. 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 10; 45(7):685-693.
    View in: PubMed
    Score: 0.236
  7. Novel recessive locus for body mass index in childhood asthma. Thorax. 2021 12; 76(12):1227-1230.
    View in: PubMed
    Score: 0.233
  8. An interaction of the 17q12-21 locus with mold exposure in childhood asthma. Pediatr Allergy Immunol. 2021 02; 32(2):373-376.
    View in: PubMed
    Score: 0.225
  9. PolyGEE: a generalized estimating equation approach to the efficient and robust estimation of polygenic effects in large-scale association studies. Biostatistics. 2018 07 01; 19(3):295-306.
    View in: PubMed
    Score: 0.192
  10. On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows. Genet Epidemiol. 2017 05; 41(4):332-340.
    View in: PubMed
    Score: 0.176
  11. On the Recombination Rate Estimation in the Presence of Population Substructure. PLoS One. 2015; 10(12):e0145152.
    View in: PubMed
    Score: 0.161
  12. Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer's disease-associated genes: DTNB and DLG2. Mol Psychiatry. 2022 Mar 04.
    View in: PubMed
    Score: 0.062
  13. A novel locus for exertional dyspnoea in childhood asthma. Eur Respir J. 2021 02; 57(2).
    View in: PubMed
    Score: 0.057
  14. locStra: Fast analysis of regional/global stratification in whole-genome sequencing studies. Genet Epidemiol. 2021 02; 45(1):82-98.
    View in: PubMed
    Score: 0.056
  15. Identification of Novel Alzheimer's Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data. Sci Rep. 2020 03 19; 10(1):5029.
    View in: PubMed
    Score: 0.054
  16. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma. Chest. 2019 12; 156(6):1068-1079.
    View in: PubMed
    Score: 0.052
  17. 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: 0.052
  18. Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project. Bioinformatics. 2016 05 01; 32(9):1366-72.
    View in: PubMed
    Score: 0.040
  19. Using Network Methodology to Infer Population Substructure. PLoS One. 2015; 10(6):e0130708.
    View in: PubMed
    Score: 0.039
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.