1.Transcription factors Sp1 and Sp3 alter vascular endothelial growth factor receptor expression through a novel recognition sequence

Hata, Y, Duh, E, Zha     More...

Hata, Y, Duh, E, Zhang, K, Robinson, GS, Aiello, LP     Less

JOURNAL OF BIOLOGICAL CHEMISTRY[0021-9258], Published 1998, Volume 273, Issue 30, Pages 19294-19303

收錄情况： WOS SCOPUS

WOS核心合集引用: 119  发表年影響因子:  7.199 

2.A new locus for autosomal dominant Stargardt-like disease maps to chromosome 4

Kniazeva, M, Chiang,     More...

Kniazeva, M, Chiang, MF, Morgan, B, Anduze, AL, Zack, DJ, Han, M, Zhang, K     Less

AMERICAN JOURNAL OF HUMAN GENETICS[0002-9297], Published 1999, Volume 64, Issue 5, Pages 1394-1399

收錄情况： WOS SCOPUS

WOS核心合集引用: 76  2023影響因子:  8.1  发表年影響因子:  10.426 

3.Discordance of primary infantile glaucoma in monozygotic twins

Zhang, K, Jampel, HD     More...

Zhang, K, Jampel, HD     Less

AMERICAN JOURNAL OF OPHTHALMOLOGY[0002-9394], Published 1999, Volume 128, Issue 1, Pages 97-98

收錄情况： WOS SCOPUS

WOS核心合集引用: 3  2023影響因子:  4.1  发表年影響因子:  2.012 

4.The ABCR gene in recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration

Zhang, K, Kniazeva,     More...

Zhang, K, Kniazeva, M, Hutchinson, A, Han, M, Dean, M, Allikmets, R     Less

GENOMICS[0888-7543], Published 1999, Volume 60, Issue 2, Pages 234-237

收錄情况： WOS SCOPUS

WOS核心合集引用: 40  2023影響因子:  3.4  发表年影響因子:  3.386 

5.The ABCR gene recessive and dominant Stargardt diseases: A genetic pathway in macular degeneration.

Zhang, K, Garibaldi,     More...

Zhang, K, Garibaldi, DC, Kniazeva, M, Hutchinson, A, Han, M, Dean, M, Allikmets, R     Less

AMERICAN JOURNAL OF HUMAN GENETICS[0002-9297], Published 1999, Volume 65, Issue 4, Pages A115-A115

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  8.1  发表年影響因子:  10.426 

6.Molecular genetics of macular degeneration

Garibaldi, DC, Zhang     More...

Garibaldi, DC, Zhang, K     Less

INTERNATIONAL OPHTHALMOLOGY CLINICS[0020-8167], Published 1999, Volume 39, Issue 4, Pages 117-142

收錄情况： WOS SCOPUS

WOS核心合集引用: 3  发表年影響因子:  0.231 

7.A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease

Zhang, K, Garibaldi,     More...

Zhang, K, Garibaldi, DC, Kniazeva, M, Albini, T, Chiang, MF, Kerrigan, M, Sunness, JS, Han, M, Allikmets, R     Less

AMERICAN JOURNAL OF OPHTHALMOLOGY[0002-9394], Published 1999, Volume 128, Issue 6, Pages 720-724

收錄情况： WOS SCOPUS

WOS核心合集引用: 13  2023影響因子:  4.1  发表年影響因子:  2.012 

8.Clinical, genetic and histopathologic studies of butterfly-shaped pattern dystrophy.

Li, Y, Zhang, K, Gar     More...

Li, Y, Zhang, K, Garibaldi, D, Green, WR, Zack, DJ     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2000, Volume 41, Issue 4, Pages S194-S194

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.373 

9.Genetic linkage study of dominantly inherited age-related macular degeneration in a large family

Garibaldi, DC, Kniaz     More...

Garibaldi, DC, Kniazeva, M, Han, M, Zhang, K     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2000, Volume 41, Issue 4, Pages S398-S398

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.373 

10.A new locus for dominant drusen and macular degeneration maps to chromosome 6q14

Kniazeva, M, Traboul     More...

Kniazeva, M, Traboulsi, EI, Yu, ZY, Stefko, ST, Gorin, MB, Shugart, YY, O'Connell, JR, Blaschak, CJ, Cutting, G, Han, M, Zhang, K     Less

AMERICAN JOURNAL OF OPHTHALMOLOGY[0002-9394], Published 2000, Volume 130, Issue 2, Pages 197-202

收錄情况： WOS SCOPUS

WOS核心合集引用: 20  2023影響因子:  4.1  发表年影響因子:  1.941 

11.Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration

Stefko, ST, Zhang, K     More...

Stefko, ST, Zhang, K, Gorin, MB, Traboulsi, EI     Less

AMERICAN JOURNAL OF OPHTHALMOLOGY[0002-9394], Published 2000, Volume 130, Issue 2, Pages 203-208

收錄情况： WOS SCOPUS

WOS核心合集引用: 9  2023影響因子:  4.1  发表年影響因子:  1.941 

12.A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy

Zhang, K, Kniazeva,     More...

Zhang, K, Kniazeva, M, Han, M, Li, W, Yu, ZY, Yang, ZL, Li, Y, Metzker, ML, Allikmets, R, Zack, DJ, Kakuk, LE, Lagali, PS, Wong, PW, MacDonald, IM, Sieving, PA, Figueroa, DJ, Austin, CP, Gould, RJ, Ayyagari, R, Petrukhin, K     Less

NATURE GENETICS[1061-4036], Published 2001, Volume 27, Issue 1, Pages 89-93

收錄情况： WOS SCOPUS

WOS核心合集引用: 351  2023影響因子:  31.8  发表年影響因子:  29.600 

13.A new deletion in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy and pattern dystrophy.

Bernstein, PS, Zabri     More...

Bernstein, PS, Zabriskie, NA, Tammur, J, Hutchinson, A, Dixon, M, Peiffer, A, Zhang, K, Petrukhin, K, Leppert, M, Allikmets, R     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S323-S323

收錄情况： WOS

WOS核心合集引用: 1  2023影響因子:  5.0  发表年影響因子:  4.172 

14.A five base-pair deletion in ELOVI4 is associated with two related forms of autosomal dominant macular dystrophy.

Zhang, K, Wong, PW,     More...

Zhang, K, Wong, PW, Ayyagari, R, Li, W, Yang, Z, Allikmets, R, Zack, DJ, Sieving, PA, Austin, CP, Petrukhin, K     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S323_S323

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.172 

15.Analysis of the ELOVL4 gene in patients with AMD and dominant macular dystrophies.

Kakuk, LE, Zhang, K,     More...

Kakuk, LE, Zhang, K, Swaroop, A, Yashar, BM, Yang, Z, Li, Y, Petrukhin, K, Sieving, PA, Ayyagari, R, Allikmets, R     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S638-S638

收錄情况： WOS

WOS核心合集引用: 1  2023影響因子:  5.0  发表年影響因子:  4.172 

16.Genetic linkage study of dominantly inherited age-related macular degeneration in a large family.

Yang, Z, O'Connor, S     More...

Yang, Z, O'Connor, ST, Yu, Z, Zhang, H, Li, Y, Traboulsi, E, Zhang, K     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S638_S638

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.172 

17.Linkage analysis of a family with dominant Stargardt's-like macular dystrophy - evidence of a novel disease locus.

O'Connor, ST, Sperbe     More...

O'Connor, ST, Sperber, D, Yang, Z, Yu, Z, Zhang, H, Li, Y, Zhang, K     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S639-S639

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.172 

18.Comprehensive mutation screen in the RGS9 gene in 558 patients with inherited retinal degenerations.

Hagstrom, SA, Zhang,     More...

Hagstrom, SA, Zhang, K, Baehr, W, He, W, Wensel, TG, Berson, EL, Dryja, TP     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S646-S646

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.172 

19.A novel mutation in the RDS/Peripherin gene associated with butterfly-shaped pattern dystrophy.

Li, Y, Moshfeghi, D,     More...

Li, Y, Moshfeghi, D, Yu, Z, Jacobson, SG, Zack, DJ, Zhang, K     Less

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[0146-0404], Published 2001, Volume 42, Issue 4, Pages S647-S647

收錄情况： WOS

WOS核心合集引用: 0  2023影響因子:  5.0  发表年影響因子:  4.172 

20.Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus

Li, Y, Marcos, I, Bo     More...

Li, Y, Marcos, I, Borrego, S, Yu, ZY, Zhang, K, Antinolo, G     Less

JOURNAL OF MEDICAL GENETICS[0022-2593], Published 2001, Volume 38, Issue 7, Pages 478-480

收錄情况： WOS SCOPUS

WOS核心合集引用: 15  2023影響因子:  3.6  发表年影響因子:  5.098