Paper Chase is a research database designed to offer abstracts of research articles published in journals that have a highly rated impact factor as determined by ISI Impact Factor and PageRank. Abstracts are organized by date, with the most recently published papers listed first. 

Paper Chase

221.

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.

Nat. Genet.
Yamamoto S, Sippel KC, Berson EL, Dryja TP.
| 2 1, 1997
222.

Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence.

Nat. Genet.
Stoffers DA, Zinkin NT, Stanojevic V, Clarke WL, Habener JF.
| 1 1, 1997
223.

UBE3A/E6-AP mutations cause Angelman syndrome.

Nat. Genet.
Kishino T, Lalande M, Wagstaff J.
| 1 1, 1997
224.

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.

Nat. Genet.
Basson CT, Bachinsky DR, Lin RC, Levi T, Elkins JA, Soults J, Grayzel D, Kroumpouzou E, Traill TA, Leblanc-Straceski J, Renault B, Kucherlapati R, Seidman JG, Seidman CE.
| 1 1, 1997
225.

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.

Nat. Genet.
Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR.
| 8 1, 1996
226.

Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease.

Nat. Genet.
Rubattu S, Volpe M, Kreutz R, Ganten U, Ganten D, Lindpaintner K.
| 8 1, 1996
227.

A human MSX1 homeodomain missense mutation causes selective tooth agenesis.

Nat. Genet.
Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
| 8 1, 1996
229.

Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat.

Nat. Genet.
Brown DM, Provoost AP, Daly MJ, Lander ES, Jacob HJ.
| 1 1, 1996
230.

A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2).

Nat. Genet.
Muragaki Y, Mariman EC, van Beersum SE, Perälä M, van Mourik JB, Warman ML, Olsen BR, Hamel BC.
| 1 1, 1996
231.

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.

Nat. Genet.
Huang SH, Pittler SJ, Huang X, Oliveira L, Berson EL, Dryja TP.
| 12 1, 1995
232.

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Nat. Genet.
Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE.
| 12 1, 1995
233.

Gene therapy of metastatic cancer by in vivo retroviral gene targeting.

Nat. Genet.
Hurford RK, Dranoff G, Mulligan RC, Tepper RI.
| 8 1, 1995
234.

Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases.

Nat. Genet.
Mashal RD, Koontz J, Sklar J.
| 2 1, 1995
235.

A genetic linkage map of the laboratory rat, Rattus norvegicus.

Nat. Genet.
Jacob HJ, Brown DM, Bunker RK, Daly MJ, Dzau VJ, Goodman A, Koike G, Kren V, Kurtz T, Lernmark A.
| 1 1, 1995
236.

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.

Nat. Genet.
Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG.
| 11 1, 1994
237.

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Nat. Genet.
Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB, Cody RJ, Fishman MC.
| 8 1, 1994
238.

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects.

Nat. Genet.
Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL.
| 8 1, 1994