G D Billingsley

Author PubWeight™ 11.82^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	The gamma-crystallins and human cataracts: a puzzle made clearer.	Am J Hum Genet	1999	2.81
2	Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.	Eur J Hum Genet	2000	1.38
3	DNA restriction-site polymorphisms associated with the alpha 1-antitrypsin gene.	Am J Hum Genet	1987	1.05
4	Restriction enzyme MaeIII for prenatal diagnosis of alpha 1-antitrypsin deficiency.	Lancet	1986	0.94
5	Physical and genetic mapping of the serpin gene cluster at 14q32.1: allelic association and a unique haplotype associated with alpha 1-antitrypsin deficiency.	Am J Hum Genet	1994	0.88
6	Rare deficiency types of alpha 1-antitrypsin: electrophoretic variation and DNA haplotypes.	Am J Hum Genet	1989	0.87
7	Aggregation of plasma Z type alpha 1-antitrypsin suggests basic defect for the deficiency.	FEBS Lett	1986	0.86
8	Functional assessment of genetic variants of alpha 1-antitrypsin.	Hum Genet	1982	0.84
9	Oxidation of plasma alpha 1-antitrypsin in smokers and nonsmokers and by an oxidizing agent.	Am Rev Respir Dis	1984	0.76
10	An RFLP associated with the human T-cell antigen receptor alpha chain locus.	Nucleic Acids Res	1987	0.75
11	CEPH consortium map of chromosome 14.	Cytogenet Cell Genet	1995	0.75
12	Functional assay of alpha 1-antitrypsin in obstructive lung disease.	Am Rev Respir Dis	1980	0.75
13	Human Myiasis: Hypoderma Bovis De G.	Cal West Med	1938	0.75