A citation-based method for searching scientific literature

Yukiko Kuroda, Ikuko Ohashi, Takuya Naruto, Kazumi Ida, Yumi Enomoto, Toshiyuki Saito, Jun-Ichi Nagai, Sadamitsu Yanagi, Hideaki Ueda, Kenji Kurosawa. J Hum Genet 2018
Times Cited: 5



Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder-Espinasse, Bruno Delobel, Bénédicte Duban, Louis Vallee, Jean-Marie Cuisset, Marie-Pierre Lemaitre, Marie-Christine Vantyghem, Marie Pigeyre, Sandrine Lanco-Dosen, Ghislaine Plessis, Marion Gerard, Matthieu Decamp, Michèle Mathieu, Gilles Morin, Guillaume Jedraszak, Frédéric Bilan, Brigitte Gilbert-Dussardier, Delphine Fauvert, Joëlle Roume, Valérie Cormier-Daire, Roseline Caumes, Jacques Puechberty, David Genevieve, Pierre Sarda, Lucie Pinson, Patricia Blanchet, Nathalie Lemeur, Frenny Sheth, Sylvie Manouvrier-Hanu, Joris Andrieux. Eur J Med Genet 2015
Times Cited: 49




List of shared articles



Times cited

Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome.
Kyle W Davis, Moises Serrano, Sara Loddo, Catherine Robinson, Viola Alesi, Bruno Dallapiccola, Antonio Novelli, Merlin G Butler. Int J Mol Sci 2019
9

15q11.2 deletion is enriched in patients with total anomalous pulmonary venous connection.
Xiaoliang Li, Guocheng Shi, Yang Li, Xiaoqing Zhang, Ying Xiang, Teng Wang, Yanxin Li, Huiwen Chen, Qihua Fu, Hong Zhang,[...]. J Med Genet 2020
1

A Rare Case of 15q11.2 Microdeletion Syndrome with Atypical Features: Diagnostic Dilemma.
Waliul Chowdhury, Pooja Patak, Farjahan J Chowdhury, Hasnan M Ijaz, Tehmina Zafar, Nick Chatla, Ahmad Khiami. Cureus 2018
1