引用次数
引用: 5,033
H-指数: 34
I10-指数 : 51
出版物: 107
Dose-dependent modulation of HIF-1α/ sima controls the rate of cell migration and invasion in Drosophila ovary border cells
S Doronkin , I Djagaeva , M E Nagle , L T Reiter
Oncogene 29 ( 8) 1123 -1134
15
2010
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent.
V Timmerman , B Rautenstrauss , L T Reiter , T Koeuth
Journal of Medical Genetics 34 ( 1) 43 -49
50
1997
Molecular Mechanisms for CMT1A Duplication and HNPP Deletion
C. F. BOERKOEL , K. INOUE , L. T. REITER , L. E. WARNER
Annals of the New York Academy of Sciences 883 ( 1) 22 -35
37
1999
Developmental Disabilities, Autism, and Schizophrenia at a Single Locus: Complex Gene Regulation and Genomic Instability of 15q11-q13 Cause a Range of Neurodevelopmental Disorders
N. Urraca , L.T. Reiter
Neural Circuit Development and Function in the Brain#R##N#Comprehensive Developmental Neuroscience 617 -630
2013
The 1.4 Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.
JL Badano , K Inoue , K Dewar , N Katsanis
AMERICAN JOURNAL OF HUMAN GENETICS 69 ( 4) 465 -465
2001
15q duplication syndrome and related disorders
Brenda M Finucane , L Lusk , D Arkilo , S Chamberlain
GeneReviews 1993 -2019
72
2016
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element (vol 12, pg 288, 1996)
LT Reiter , T Murakami , T Koeuth , L Pentao
NATURE GENETICS 19 ( 3) 303 -303
1998
Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies
LE Warner , LT Reiter , T Murakami , JR Lupski
Cold Spring Harbor symposia on quantitative biology 61 659 -671
9
1996
A POSSIBLE RECOMBINATION HOT-SPOT ASSOCIATED WITH THE CMT1A DUPLICATION AND HNPP DELETION
LT Reiter , T Koeuth , P MURAKAMI , P LIU
AMERICAN JOURNAL OF HUMAN GENETICS 57 ( 4) 100 -100
1
1995
The human COX10 gene spans the 24,011-bp distal CMT1A-REP and is disrupted by the HNPP deletion.
LT Reiter , T Murakami , T Koeuth , RA Gibbs
AMERICAN JOURNAL OF HUMAN GENETICS 61 ( 4) A43 -A43
1997
Construction of a PAC contig of the 1.5 Mb CMT1A duplication HNPP deletion region in 17p11. 2-p12 for the purpose of a large scale sequencing effort.
K Inoue , T Murakami , LT Reiter , T Koeuth
AMERICAN JOURNAL OF HUMAN GENETICS 61 ( 4) A235 -A235
1997
Are mariner transposons responsible for some chromosomal deletions and duplications in humans?
JR Lupski , T Liehr , LT Reiter , B Rautenstrauss
AMERICAN JOURNAL OF HUMAN GENETICS 61 ( 4) A133 -A133
1997
A search for targets mediating Angelman syndrome pathogenesis using Drosophila melanogaster.
M Bowers , LT Reiter , YH Jiang , AL Beaudet
AMERICAN JOURNAL OF HUMAN GENETICS 69 ( 4) 634 -634
2001
Comprehensive Developmental Neuroscience: Neural Circuit Development and Function in the Heathy and Diseased Brain: Chapter 32. Developmental Disabilities, Autism, and Schizophrenia at a Single Locus: Complex Gene Regulation and Genomic Instability of 15q11–q13 Cause a Range of Neurodevelopmental Disorders
N Urraca , LT Reiter
Elsevier Inc. Chapters
1
2013
Misexpression of 50 uncharacterized Drosophila homologs to human disease genes reveals insight into gene function.
D Huffman , LT Reiter , E Bier
American Journal of Human Genetics 69 ( 4) 469 -469
1
2001
Mutations in the Drosophila homolog of the gene for primary congenital glaucoma cause fluid flow and neurological defects.
LT Reiter , M McElroy , BB Bejjani , E Bier
AMERICAN JOURNAL OF HUMAN GENETICS 69 ( 4) 653 -653
1
2001
Using Drosophila melanogaster to identify Angelman syndrome therapeutic targets.
LT Reiter , M Bowers , E Bier
AMERICAN JOURNAL OF HUMAN GENETICS 71 ( 4) 526 -526
2002
15q Duplication Syndrome and Related Disorders GeneReviews®
BM Finucane , L Lusk , D Arkilo , S Chamberlain
Seattle: University of Washington, Seattle 2018
5
1993
Genomic Structure and Expression of the Human Heme A:Farnesyltransferase (COX10) Gene
Tatsufumi Murakami , Lawrence T. Reiter , James R. Lupski
Genomics 42 ( 1) 161 -164
24
1997
A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism.
Nora Urraca , Brian Potter , Rachel Hundley , Eniko K. Pivnick
Frontiers in Genetics 7 205 -205
4
2016