A citation-based method for searching scientific literature

E M Rinchik, S J Bultman, B Horsthemke, S T Lee, K M Strunk, R A Spritz, K M Avidano, M T Jong, R D Nicholls. Nature 1993
Times Cited: 323







List of co-cited articles
789 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.
J M Newton, O Cohen-Barak, N Hagiwara, J M Gardner, M T Davisson, R A King, M H Brilliant. Am J Hum Genet 2001
219
31

Aberrant pH of melanosomes in pink-eyed dilution (p) mutant melanocytes.
N Puri, J M Gardner, M H Brilliant. J Invest Dermatol 2000
121
28

The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes.
J M Gardner, Y Nakatsu, Y Gondo, S Lee, M F Lyon, R A King, M H Brilliant. Science 1992
196
25


Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene.
S Rosemblat, D Durham-Pierre, J M Gardner, Y Nakatsu, M H Brilliant, S J Orlow. Proc Natl Acad Sci U S A 1994
119
23

Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".
R E Boissy, H Zhao, W S Oetting, L M Austin, S C Wildenberg, Y L Boissy, Y Zhao, R A Sturm, V J Hearing, R A King,[...]. Am J Hum Genet 1996
138
22

Pink-eyed dilution protein controls the processing of tyrosinase.
Kun Chen, Prashiela Manga, Seth J Orlow. Mol Biol Cell 2002
95
23


Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene.
Y Tomita, A Takeda, S Okinaga, H Tagami, S Shibahara. Biochem Biophys Res Commun 1989
162
21

The etiology of oculocutaneous albinism (OCA) type II: the pink protein modulates the processing and transport of tyrosinase.
Kazutomo Toyofuku, Julio C Valencia, Tsuneto Kushimoto, Gertrude-E Costin, Victoria M Virador, Wilfred D Vieira, Victor J Ferrans, Vincent J Hearing. Pigment Cell Res 2002
81
25

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.
David L Duffy, Grant W Montgomery, Wei Chen, Zhen Zhen Zhao, Lien Le, Michael R James, Nicholas K Hayward, Nicholas G Martin, Richard A Sturm. Am J Hum Genet 2007
144
19

Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan.
Katsuhiko Inagaki, Tamio Suzuki, Hiroshi Shimizu, Norihisa Ishii, Yoshinori Umezawa, Joji Tada, Noriaki Kikuchi, Minoru Takata, Kenji Takamori, Mari Kishibe,[...]. Am J Hum Genet 2004
88
20

SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans.
Rebecca L Lamason, Manzoor-Ali P K Mohideen, Jason R Mest, Andrew C Wong, Heather L Norton, Michele C Aros, Michael J Jurynec, Xianyun Mao, Vanessa R Humphreville, Jasper E Humbert,[...]. Science 2005
653
18

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.
Richard A Sturm, David L Duffy, Zhen Zhen Zhao, Fabio P N Leite, Mitchell S Stark, Nicholas K Hayward, Nicholas G Martin, Grant W Montgomery. Am J Hum Genet 2008
228
18

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression.
Hans Eiberg, Jesper Troelsen, Mette Nielsen, Annemette Mikkelsen, Jonas Mengel-From, Klaus W Kjaer, Lars Hansen. Hum Genet 2008
196
18

Oculocutaneous albinism.
Karen Grønskov, Jakob Ek, Karen Brondum-Nielsen. Orphanet J Rare Dis 2007
229
18

Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma.
Anne-Sophie Jannot, Roubila Meziani, Guylene Bertrand, Benedicte Gérard, Vincent Descamps, Alain Archimbaud, Catherine Picard, Laurence Ollivaud, Nicole Basset-Seguin, Delphine Kerob,[...]. Eur J Hum Genet 2005
70
24


Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.
S T Lee, R D Nicholls, S Bundey, R Laxova, M Musarella, R A Spritz. N Engl J Med 1994
164
16

Genetic determinants of hair, eye and skin pigmentation in Europeans.
Patrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, Agnar Helgason, Thorunn Rafnar, Kristinn P Magnusson, Andrei Manolescu, Ari Karason, Arnar Palsson, Gudmar Thorleifsson,[...]. Nat Genet 2007
459
16

Increasing the complexity: new genes and new types of albinism.
Lluís Montoliu, Karen Grønskov, Ai-Hua Wei, Mónica Martínez-García, Almudena Fernández, Benoît Arveiler, Fanny Morice-Picard, Saima Riazuddin, Tamio Suzuki, Zubair M Ahmed,[...]. Pigment Cell Melanoma Res 2014
115
15

Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 function.
Anand Sitaram, Rosanna Piccirillo, Ilaria Palmisano, Dawn C Harper, Esteban C Dell'Angelica, M Vittoria Schiaffino, Michael S Marks. Mol Biol Cell 2009
51
25

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.
Ai-Hua Wei, Dong-Jie Zang, Zhe Zhang, Xuan-Zhu Liu, Xin He, Lin Yang, Yi Wang, Zhi-Yong Zhou, Ming-Rong Zhang, Lan-Lan Dai,[...]. J Invest Dermatol 2013
63
20


Pink-eyed dilution protein modulates arsenic sensitivity and intracellular glutathione metabolism.
Liliana Staleva, Prashiela Manga, Seth J Orlow. Mol Biol Cell 2002
46
26

Birth prevalence and mutation spectrum in danish patients with autosomal recessive albinism.
Karen Grønskov, Jakob Ek, Annie Sand, Rudolf Scheller, Anette Bygum, Kim Brixen, Karen Brondum-Nielsen, Thomas Rosenberg. Invest Ophthalmol Vis Sci 2009
51
23


Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinism.
Karen Grønskov, Christopher M Dooley, Elsebet Østergaard, Robert N Kelsh, Lars Hansen, Mitchell P Levesque, Kaj Vilhelmsen, Kjeld Møllgård, Derek L Stemple, Thomas Rosenberg. Am J Hum Genet 2013
57
19

Sequences associated with human iris pigmentation.
Tony Frudakis, Matthew Thomas, Zach Gaskin, K Venkateswarlu, K Suresh Chandra, Siva Ginjupalli, Sitaram Gunturi, Sivamani Natrajan, Viswanathan K Ponnuswamy, K N Ponnuswamy. Genetics 2003
87
11

P gene as an inherited biomarker of human eye color.
Timothy R Rebbeck, Peter A Kanetsky, Amy H Walker, Robin Holmes, Allan C Halpern, Lynn M Schuchter, David E Elder, DuPont Guerry. Cancer Epidemiol Biomarkers Prev 2002
62
16

The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.
M Ramsay, M A Colman, G Stevens, E Zwane, J Kromberg, M Farrall, T Jenkins. Am J Hum Genet 1992
88
11


Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism.
Meredith E Protas, Candace Hersey, Dawn Kochanek, Yi Zhou, Horst Wilkens, William R Jeffery, Leonard I Zon, Richard Borowsky, Clifford J Tabin. Nat Genet 2006
305
10

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
Jiali Han, Peter Kraft, Hongmei Nan, Qun Guo, Constance Chen, Abrar Qureshi, Susan E Hankinson, Frank B Hu, David L Duffy, Zhen Zhen Zhao,[...]. PLoS Genet 2008
329
10


OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24.
T Kausar, M A Bhatti, M Ali, R S Shaikh, Z M Ahmed. Clin Genet 2013
51
19


Eye colour: portals into pigmentation genes and ancestry.
Richard A Sturm, Tony N Frudakis. Trends Genet 2004
77
11

Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.
P Manga, J G Kromberg, N F Box, R A Sturm, T Jenkins, M Ramsay. Am J Hum Genet 1997
86
10

Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4.
Uta Rundshagen, Christine Zühlke, Sven Opitz, Eberhard Schwinger, Barbara Käsmann-Kellner. Hum Mutat 2004
50
18

The color loci of mice--a genetic century.
Dorothy C Bennett, M Lynn Lamoreux. Pigment Cell Res 2003
323
9

Melanosomal defects in melanocytes from mice lacking expression of the pink-eyed dilution gene: correction by culture in the presence of excess tyrosine.
S Rosemblat, E V Sviderskaya, D J Easty, A Wilson, B S Kwon, D C Bennett, S J Orlow. Exp Cell Res 1998
44
20

A comprehensive genetic study of autosomal recessive ocular albinism in Caucasian patients.
Saunie M Hutton, Richard A Spritz. Invest Ophthalmol Vis Sci 2008
70
12

Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1-4 genes and practical aspects.
Caroline Rooryck, Fanny Morice-Picard, Nursel H Elçioglu, Didier Lacombe, Alain Taieb, Benoît Arveiler. Pigment Cell Melanoma Res 2008
63
14

DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.
Dimitre R Simeonov, Xinjing Wang, Chen Wang, Yuri Sergeev, Monika Dolinska, Matthew Bower, Roxanne Fischer, David Winer, Genia Dubrovsky, Joan Z Balog,[...]. Hum Mutat 2013
72
12

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.
David L Duffy, Neil F Box, Wei Chen, James S Palmer, Grant W Montgomery, Michael R James, Nicholas K Hayward, Nicholas G Martin, Richard A Sturm. Hum Mol Genet 2004
193
8

P gene mutations associated with oculocutaneous albinism type II (OCA2).
William S Oetting, Sarah Savage Garrett, Marcia Brott, Richard A King. Hum Mutat 2005
41
19

Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes.
Katsuhiko Inagaki, Tamio Suzuki, Shiro Ito, Noriyuki Suzuki, Koji Adachi, Torayuki Okuyama, Yusei Nakata, Hiroshi Shimizu, Hironori Matsuura, Takashi Oono,[...]. Pigment Cell Res 2006
29
27

Genetic evidence for the convergent evolution of light skin in Europeans and East Asians.
Heather L Norton, Rick A Kittles, Esteban Parra, Paul McKeigue, Xianyun Mao, Keith Cheng, Victor A Canfield, Daniel G Bradley, Brian McEvoy, Mark D Shriver. Mol Biol Evol 2007
247
8

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.
Manfred Kayser, Fan Liu, A Cecile J W Janssens, Fernando Rivadeneira, Oscar Lao, Kate van Duijn, Mark Vermeulen, Pascal Arp, Mila M Jhamai, Wilfred F J van Ijcken,[...]. Am J Hum Genet 2008
153
8


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.