A citation-based method for searching scientific literature

Hande Kocak, Bari J Ballew, Kamlesh Bisht, Rebecca Eggebeen, Belynda D Hicks, Shalabh Suman, Adri O'Neil, Neelam Giri, Ivan Maillard, Blanche P Alter, Catherine E Keegan, Jayakrishnan Nandakumar, Sharon A Savage. Genes Dev 2014
Times Cited: 70







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



Times Cited
  Times     Co-cited
Similarity


SNMIB/Apollo protects leading-strand telomeres against NHEJ-mediated repair.
Yung C Lam, Shamima Akhter, Peili Gu, Jing Ye, Anaïs Poulet, Marie-Josèphe Giraud-Panis, Susan M Bailey, Eric Gilson, Randy J Legerski, Sandy Chang. EMBO J 2010
81
1

MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway.
Ralph Gruber, Zhongwei Zhou, Mikhail Sukchev, Tjard Joerss, Pierre-Olivier Frappart, Zhao-Qi Wang. Nat Cell Biol 2011
148
1

A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome.
Mark O'Driscoll, Victor L Ruiz-Perez, C Geoffrey Woods, Penny A Jeggo, Judith A Goodship. Nat Genet 2003
565
1

The annealing helicase SMARCAL1 maintains genome integrity at stalled replication forks.
Carol E Bansbach, Rémy Bétous, Courtney A Lovejoy, Gloria G Glick, David Cortez. Genes Dev 2009
167
1

Solving the Telomere Replication Problem.
Laetitia Maestroni, Samah Matmati, Stéphane Coulon. Genes (Basel) 2017
40
2



BRIT1/MCPH1 is a DNA damage responsive protein that regulates the Brca1-Chk1 pathway, implicating checkpoint dysfunction in microcephaly.
Shiaw-Yih Lin, Rekha Rai, Kaiyi Li, Zhi-Xiang Xu, Stephen J Elledge. Proc Natl Acad Sci U S A 2005
128
1

Neurogenesis requires TopBP1 to prevent catastrophic replicative DNA damage in early progenitors.
Youngsoo Lee, Sachin Katyal, Susanna M Downing, Jingfeng Zhao, Helen R Russell, Peter J McKinnon. Nat Neurosci 2012
39
2

The Replisome Mediates A-NHEJ Repair of Telomeres Lacking POT1-TPP1 Independently of MRN Function.
Rekha Rai, Peili Gu, Cayla Broton, Chandan Kumar-Sinha, Yong Chen, Sandy Chang. Cell Rep 2019
6
16

A terminal long arm deletion of chromosome 16 in a dysmorphic infant: 46,XY,del(16) (q22).
K Taysi, M Fishman, G S Sekhon. Birth Defects Orig Artic Ser 1978
11
9

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
1

CTCF deletion syndrome: clinical features and epigenetic delineation.
Ikumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, Hidetaka Watanabe, Ken Higashimoto, Junko Tomikawa, Daisuke Ieda, Kei Ohashi, Yutaka Negishi, Ayako Hattori,[...]. J Med Genet 2017
11
9

Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics.
Linn Fagerberg, Björn M Hallström, Per Oksvold, Caroline Kampf, Dijana Djureinovic, Jacob Odeberg, Masato Habuka, Simin Tahmasebpoor, Angelika Danielsson, Karolina Edlund,[...]. Mol Cell Proteomics 2014
450
1

Interstitial 16q deletion with typical dysmorphic syndrome.
J P Fryns, W Proesmans, G Van Hoey, H Van den Berghe. Ann Genet 1981
30
3

TINF2 is a haploinsufficient tumor suppressor that limits telomere length.
Isabelle Schmutz, Arjen R Mensenkamp, Kaori K Takai, Maaike Haadsma, Liesbeth Spruijt, Richarda M de Voer, Seunga Sara Choo, Franziska K Lorbeer, Emma J van Grinsven, Dirk Hockemeyer,[...]. Elife 2020
2
50

Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics.
Linn Fagerberg, Björn M Hallström, Per Oksvold, Caroline Kampf, Dijana Djureinovic, Jacob Odeberg, Masato Habuka, Simin Tahmasebpoor, Angelika Danielsson, Karolina Edlund,[...]. Mol Cell Proteomics 2014
1

One protein to rule them all: The role of CCCTC-binding factor in shaping human genome in health and disease.
Michal Lazniewski, Wayne K Dawson, Anna Maria Rusek, Dariusz Plewczynski. Semin Cell Dev Biol 2019
7
14

Pulmonary fibrosis linked to variants in the ACD gene, encoding the telomere protein TPP1.
Thijs W Hoffman, Joanne J van der Vis, Jasper J van der Smagt, Maarten P G Massink, Jan C Grutters, Coline H M van Moorsel. Eur Respir J 2019
4
25


Prognostic significance of pulmonary function tests in dyskeratosis congenita, a telomere biology disorder.
Neelam Giri, Sandhiya Ravichandran, Youjin Wang, Shahinaz M Gadalla, Blanche P Alter, Joseph Fontana, Sharon A Savage. ERJ Open Res 2019
5
20


Monosomy 16q: a distinct syndrome. Apropos of a de novo del(16) (q2100q2300).
H Rivera, E Vargas-Moyeda, M Möller, A Torres-Lamas, J M Cantú. Clin Genet 1985
24
4


Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes.
Elena G Arias-Salgado, Eva Galvez, Lurdes Planas-Cerezales, Laura Pintado-Berninches, Elena Vallespin, Pilar Martinez, Jaime Carrillo, Laura Iarriccio, Anna Ruiz-Llobet, Albert Catalá,[...]. Orphanet J Rare Dis 2019
9
11


A Truncating Germline Mutation of TINF2 in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres.
Huiling He, Wei Li, Daniel F Comiskey, Sandya Liyanarachchi, Taina T Nieminen, Yanqiang Wang, Katherine E DeLap, Pamela Brock, Albert de la Chapelle. Thyroid 2020
11
9

Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis.
A Cooke, J Tolmie, W Darlington, E Boyd, R Thomson, M A Ferguson-Smith. J Med Genet 1987
33
3

Interstitial deletion for a region in the long arm of chromosome 16.
C C Lin, R B Lowry, F F Snyder. Hum Genet 1983
33
3

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.
C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward. Genet Med 2008
517
1

16q22.1 microdeletion and anticipatory guidance.
Sarah Abdullah, Mayada Helal, Lucie Dupuis, D James Stavropoulos, Pedro Louro, Lina Ramos, Roberto Mendoza-Londono. Am J Med Genet A 2019
1
100

Skewed X-inactivation in carriers of X-linked dyskeratosis congenita.
T J Vulliamy, S W Knight, I Dokal, P J Mason. Blood 1997
50
2

Telomerase RNA mutated in autosomal dyskeratosis congenita reconstitutes a weakly active telomerase enzyme defective in telomere elongation.
Maria Antonietta Cerone, Ryan J Ward, J Arturo Londoño-Vallejo, Chantal Autexier. Cell Cycle 2005
22
4

Near-maximal expansions of hematopoietic stem cells in culture using NUP98-HOX fusions.
Hideaki Ohta, Sanja Sekulovic, Silvia Bakovic, Connie J Eaves, Nicolas Pineault, Maura Gasparetto, Clayton Smith, Guy Sauvageau, R Keith Humphries. Exp Hematol 2007
43
2

Ontogeny stage-independent and high-level clonal expansion in vitro of mouse hematopoietic stem cells stimulated by an engineered NUP98-HOX fusion transcription factor.
Sanja Sekulovic, Maura Gasparetto, Véronique Lecault, Corinne A Hoesli, David G Kent, Patty Rosten, Adrian Wan, Christy Brookes, Carl L Hansen, James M Piret,[...]. Blood 2011
14
7

Prolonged self-renewal activity unmasks telomerase control of telomere homeostasis and function of mouse hematopoietic stem cells.
Sanja Sekulovic, Vala Gylfadottir, Irma Vulto, Maura Gasparetto, Yasmine Even, Christy Brookes, Clayton Smith, Connie J Eaves, Peter M Lansdorp, Fabio M Rossi,[...]. Blood 2011
14
7

Molecular mechanisms of telomere biology disorders.
Sherilyn Grill, Jayakrishnan Nandakumar. J Biol Chem 2021
3
33

Mastermind critically regulates Notch-mediated lymphoid cell fate decisions.
Ivan Maillard, Andrew P Weng, Andrea C Carpenter, Carlos G Rodriguez, Hong Sai, Lanwei Xu, David Allman, Jon C Aster, Warren S Pear. Blood 2004
227
1


Structural Basis for Shelterin Bridge Assembly.
Jin-Kwang Kim, Jinqiang Liu, Xichan Hu, Clinton Yu, Kyle Roskamp, Banumathi Sankaran, Lan Huang, Elizabeth A Komives, Feng Qiao. Mol Cell 2017
18
5

Exclusive development of T cell neoplasms in mice transplanted with bone marrow expressing activated Notch alleles.
W S Pear, J C Aster, M L Scott, R P Hasserjian, B Soffer, J Sklar, D Baltimore. J Exp Med 1996
556
1


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.