(Q39537322)

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Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects

scientific article published on December 2011

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scholarly article

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Europe PubMed Central

PMC publication ID

12 September 2017

Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects (English)

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

author name string

Nengjun Yi

1

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Nianjun Liu

2

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Degui Zhi

3

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Europe PubMed Central

PMC publication ID

12 September 2017

Jun Li

4

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Europe PubMed Central

PMC publication ID

12 September 2017

publication date

1 December 2011

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Europe PubMed Central

PMC publication ID

12 September 2017

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Europe PubMed Central

PMC publication ID

12 September 2017

7

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Europe PubMed Central

PMC publication ID

12 September 2017

12

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

e1002382

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

copyright license

Creative Commons Attribution 4.0 International

1 December 2011

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April 2022 Public Data File from Crossref

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1 reference

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1 reference

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10.1371/JOURNAL.PGEN.1002382

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PubMed publication ID

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Europe PubMed Central

PMC publication ID

12 September 2017

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