A A Lin
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Explore the profile of A A Lin including associated specialties, affiliations and a list of published articles.
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20
Citations
1254
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Recent Articles
1.
King R, Ozcan S, Carter T, Kalfoglu E, Atasoy S, Triantaphyllidis C, et al.
Ann Hum Genet
. 2008 Feb;
72(Pt 2):205-14.
PMID: 18269686
The earliest Neolithic sites of Europe are located in Crete and mainland Greece. A debate persists concerning whether these farmers originated in neighboring Anatolia and the role of maritime colonization....
2.
Francalacci P, Morelli L, Underhill P, Lillie A, Passarino G, Useli A, et al.
Am J Phys Anthropol
. 2003 May;
121(3):270-9.
PMID: 12772214
An informative set of biallelic polymorphisms was used to study the structure of Y-chromosome variability in a sample from the Mediterranean islands of Corsica and Sicily, and compared with data...
3.
Gresham D, Morar B, Underhill P, Passarino G, Lin A, Wise C, et al.
Am J Hum Genet
. 2001 Nov;
69(6):1314-31.
PMID: 11704928
The identification of a growing number of novel Mendelian disorders and private mutations in the Roma (Gypsies) points to their unique genetic heritage. Linguistic evidence suggests that they are of...
4.
Underhill P, Passarino G, Lin A, Shen P, Lahr M, Foley R, et al.
Ann Hum Genet
. 2001 Jun;
65(Pt 1):43-62.
PMID: 11415522
Although molecular genetic evidence continues to accumulate that is consistent with a recent common African ancestry of modern humans, its ability to illuminate regional histories remains incomplete. A set of...
5.
Underhill P, Passarino G, Lin A, Marzuki S, Oefner P, Cavalli-Sforza L, et al.
Hum Mutat
. 2001 Apr;
17(4):271-80.
PMID: 11295824
An assessment of 28 pertinent binary genetic markers on the non-recombining portion of the Y chromosome (NRY) in New Zealand Maori and other relevant populations has revealed a diverse genetic...
6.
Passarino G, Shen P, Van Kirk J, Lin A, De Benedictis G, Cavalli Sforza L, et al.
Genomics
. 2001 Feb;
71(1):118-22.
PMID: 11161804
We have identified a dense set of markers useful in association studies involving the Werner syndrome (WRN) gene. The homozygotic disruption of the WRN gene is the cause of Werner...
7.
Semino O, Passarino G, Oefner P, Lin A, Arbuzova S, Beckman L, et al.
Science
. 2000 Nov;
290(5494):1155-9.
PMID: 11073453
A genetic perspective of human history in Europe was derived from 22 binary markers of the nonrecombining Y chromosome (NRY). Ten lineages account for >95% of the 1007 European Y...
8.
Underhill P, Shen P, Lin A, Jin L, Passarino G, Yang W, et al.
Nat Genet
. 2000 Nov;
26(3):358-61.
PMID: 11062480
Binary polymorphisms associated with the non-recombining region of the human Y chromosome (NRY) preserve the paternal genetic legacy of our species that has persisted to the present, permitting inference of...
9.
Mitsuyasu R, Anton P, Deeks S, Scadden D, Connick E, Downs M, et al.
Blood
. 2000 Jul;
96(3):785-93.
PMID: 10910888
We have genetically engineered CD4(+) and CD8(+) T cells with human immunodeficiency virus (HIV) specificity by inserting a gene, CD4zeta, containing the extracellular domain of human CD4 (which binds HIV...
10.
Shen P, Wang F, Underhill P, Franco C, Yang W, Roxas A, et al.
Proc Natl Acad Sci U S A
. 2000 Jun;
97(13):7354-9.
PMID: 10861003
Some insight into human evolution has been gained from the sequencing of four Y chromosome genes. Primary genomic sequencing determined gene SMCY to be composed of 27 exons that comprise...