A citation-based method for searching scientific literature

Kasturee Jagirdar, Darren J Smit, Stephen A Ainger, Katie J Lee, Darren L Brown, Brett Chapman, Zhen Zhen Zhao, Grant W Montgomery, Nicholas G Martin, Jennifer L Stow, David L Duffy, Richard A Sturm. Pigment Cell Melanoma Res 2014
Times Cited: 30







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



Times Cited
  Times     Co-cited
Similarity


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
120
43

Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B).
Chelsea S Norman, Luke O'Gorman, Jane Gibson, Reuben J Pengelly, Diana Baralle, J Arjuna Ratnayaka, Helen Griffiths, Matthew Rose-Zerilli, Megan Ranger, David Bunyan,[...]. Sci Rep 2017
30
30

Molecular characterization of a series of 990 index patients with albinism.
Eulalie Lasseaux, Claudio Plaisant, Vincent Michaud, Perrine Pennamen, Aurelien Trimouille, Laetitia Gaston, Solène Monfermé, Didier Lacombe, Caroline Rooryck, Fanny Morice-Picard,[...]. Pigment Cell Melanoma Res 2018
58
30

The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism.
William S Oetting, Jacy Pietsch, Marcia J Brott, Sarah Savage, James P Fryer, C Gail Summers, Richard A King. Am J Med Genet A 2009
26
30

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
76
26

A polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathway.
Christian Praetorius, Christine Grill, Simon N Stacey, Alexander M Metcalf, David U Gorkin, Kathleen C Robinson, Eric Van Otterloo, Reuben S Q Kim, Kristin Bergsteinsdottir, Margret H Ogmundsdottir,[...]. Cell 2013
127
23


A comprehensive genetic study of autosomal recessive ocular albinism in Caucasian patients.
Saunie M Hutton, Richard A Spritz. Invest Ophthalmol Vis Sci 2008
73
23


Molecular and functional studies of tyrosinase variants among Indian oculocutaneous albinism type 1 patients.
Moumita Chaki, Mainak Sengupta, Maitreyee Mondal, Abhisek Bhattacharya, Shampa Mallick, Ranjan Bhadra, Kunal Ray. J Invest Dermatol 2011
33
23

A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1.
Karen Grønskov, Cathrine Jespersgaard, Gitte Hoffmann Bruun, Pernille Harris, Karen Brøndum-Nielsen, Brage S Andresen, Thomas Rosenberg. Sci Rep 2019
21
33

Oculocutaneous albinism spectrum.
Pei-Wen Chiang, Elaine Spector, Anne Chun-Hui Tsai. Am J Med Genet A 2009
16
37

Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype.
Richard A King, Jacy Pietsch, James P Fryer, Sarah Savage, Marcia J Brott, Isabelle Russell-Eggitt, C Gail Summers, William S Oetting. Hum Genet 2003
102
20

Oculocutaneous albinism.
Karen Grønskov, Jakob Ek, Karen Brondum-Nielsen. Orphanet J Rare Dis 2007
249
20

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
67
20

Genome-wide association study of tanning phenotype in a population of European ancestry.
Hongmei Nan, Peter Kraft, Abrar A Qureshi, Qun Guo, Constance Chen, Susan E Hankinson, Frank B Hu, Gilles Thomas, Robert N Hoover, Stephen Chanock,[...]. J Invest Dermatol 2009
101
20

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
236
20

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
477
20

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
58
20

Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P loci.
Anthony L Cook, Wei Chen, Amy E Thurber, Darren J Smit, Aaron G Smith, Timothy G Bladen, Darren L Brown, David L Duffy, Lorenza Pastorino, Giovanna Bianchi-Scarra,[...]. J Invest Dermatol 2009
83
16

Two novel tyrosinase (TYR) gene mutations with pathogenic impact on oculocutaneous albinism type 1 (OCA1).
Vadieh Ghodsinejad Kalahroudi, Behnam Kamalidehghan, Ahoura Arasteh Kani, Omid Aryani, Mahdi Tondar, Fatemeh Ahmadipour, Lip Yong Chung, Massoud Houshmand. PLoS One 2014
23
21

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
339
16

Importance of nonsynonymous OCA2 variants in human eye color prediction.
Jeppe D Andersen, Carlotta Pietroni, Peter Johansen, Mikkel M Andersen, Vania Pereira, Claus Børsting, Niels Morling. Mol Genet Genomic Med 2016
17
29

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
David L Duffy, Zhen Z Zhao, Richard A Sturm, Nicholas K Hayward, Nicholas G Martin, Grant W Montgomery. J Invest Dermatol 2010
132
16

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
16

Human pigmentation genes under environmental selection.
Richard A Sturm, David L Duffy. Genome Biol 2012
94
16

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
16

Oculocutaneous albinism type 1: link between mutations, tyrosinase conformational stability, and enzymatic activity.
Monika B Dolinska, Nicole J Kus, S Katie Farney, Paul T Wingfield, Brian P Brooks, Yuri V Sergeev. Pigment Cell Melanoma Res 2017
26
19

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
667
16

The Phenotypic Spectrum of Albinism.
Charlotte C Kruijt, Gerard C de Wit, Arthur A Bergen, Ralph J Florijn, Nicoline E Schalij-Delfos, Maria M van Genderen. Ophthalmology 2018
45
16


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
64
13


Endoplasmic reticulum retention is a common defect associated with tyrosinase-negative albinism.
R Halaban, S Svedine, E Cheng, Y Smicun, R Aron, D N Hebert. Proc Natl Acad Sci U S A 2000
137
13

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
223
13


Membrane-Associated Transporter Protein (MATP) Regulates Melanosomal pH and Influences Tyrosinase Activity.
Bum-Ho Bin, Jinhyuk Bhin, Seung Ha Yang, Misun Shin, Yeon-Ju Nam, Dong-Hwa Choi, Dong Wook Shin, Ai-Young Lee, Daehee Hwang, Eun-Gyung Cho,[...]. PLoS One 2015
52
13

Molecular genetics of human pigmentation diversity.
Richard A Sturm. Hum Mol Genet 2009
222
13

Genome-wide association study identifies three loci associated with melanoma risk.
D Timothy Bishop, Florence Demenais, Mark M Iles, Mark Harland, John C Taylor, Eve Corda, Juliette Randerson-Moor, Joanne F Aitken, Marie-Francoise Avril, Esther Azizi,[...]. Nat Genet 2009
337
13

Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
Fan Liu, Mijke Visser, David L Duffy, Pirro G Hysi, Leonie C Jacobs, Oscar Lao, Kaiyin Zhong, Susan Walsh, Lakshmi Chaitanya, Andreas Wollstein,[...]. Hum Genet 2015
84
13

Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients.
Richard A Sturm, Carly Fox, Phil McClenahan, Kasturee Jagirdar, Maider Ibarrola-Villava, Parastoo Banan, Nicola C Abbott, Gloria Ribas, Brian Gabrielli, David L Duffy,[...]. J Invest Dermatol 2014
54
13

Unrevealing the role of P-protein on melanosome biology and structure, using siRNA-mediated down regulation of OCA2.
Sangjoo Park, V K Morya, Dong Hoang Nguyen, Birendra K Singh, Hyang-Bok Lee, Eun-Ki Kim. Mol Cell Biochem 2015
16
25

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.
David L Duffy, Mark M Iles, Dan Glass, Gu Zhu, Jennifer H Barrett, Veronica Höiom, Zhen Z Zhao, Richard A Sturm, Nicole Soranzo, Chris Hammond,[...]. Am J Hum Genet 2010
94
13

Association of melanogenesis genes with skin color variation among Japanese females.
Yuko Abe, Gen Tamiya, Tomohiro Nakamura, Yutaka Hozumi, Tamio Suzuki. J Dermatol Sci 2013
25
16

Two newly identified genetic determinants of pigmentation in Europeans.
Patrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, Agnar Helgason, Thorunn Rafnar, Margret Jakobsdottir, Stacy Steinberg, Sigurjon A Gudjonsson, Arnar Palsson, Gudmar Thorleifsson,[...]. Nat Genet 2008
257
13

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
13


The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
13

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
13

Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?
Mervyn G Thomas, Anil Kumar, Sarim Mohammad, Frank A Proudlock, Elizabeth C Engle, Caroline Andrews, Wai-Man Chan, Shery Thomas, Irene Gottlob. Ophthalmology 2011
235
13


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.