A citation-based method for searching scientific literature

Rebecca A Rojas, Anna A Kutateladze, Lacey Plummer, Maria Stamou, David L Keefe, Kathyrn B Salnikov, Angela Delaney, Janet E Hall, Ruslan Sadreyev, Fei Ji, Eric Fliers, Katarina Gambosova, Richard Quinton, Paulina M Merino, Veronica Mericq, Stephanie B Seminara, William F Crowley, Ravikumar Balasubramanian. Genet Med 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
Ulrich Boehm, Pierre-Marc Bouloux, Mehul T Dattani, Nicolas de Roux, Catherine Dodé, Leo Dunkel, Andrew A Dwyer, Paolo Giacobini, Jean-Pierre Hardelin, Anders Juul,[...]. Nat Rev Endocrinol 2015
358
100

From nose to fertility: the long migratory journey of gonadotropin-releasing hormone neurons.
Anna Cariboni, Roberto Maggi, John G Parnavelas. Trends Neurosci 2007
63
100

A Novel SEMA3G Mutation in Two Siblings Affected by Syndromic GnRH Deficiency.
Roberto Oleari, Valentina André, Antonella Lettieri, Sophia Tahir, Lise Roth, Alyssa Paganoni, Ivano Eberini, Chiara Parravicini, Valeria Scagliotti, Ludovica Cotellessa,[...]. Neuroendocrinology 2021
6
100

Nasal Placode Development, GnRH Neuronal Migration and Kallmann Syndrome.
Hyun-Ju Cho, Yufei Shan, Niteace C Whittington, Susan Wray. Front Cell Dev Biol 2019
20
100

Neural crest and ectodermal cells intermix in the nasal placode to give rise to GnRH-1 neurons, sensory neurons, and olfactory ensheathing cells.
Paolo Emanuele Forni, Carol Taylor-Burds, Vida Senkus Melvin, Trevor Williams, Susan Wray. J Neurosci 2011
126
100

Gli3 Regulates Vomeronasal Neurogenesis, Olfactory Ensheathing Cell Formation, and GnRH-1 Neuronal Migration.
Ed Zandro M Taroc, Ankana S Naik, Jennifer M Lin, Nicolas B Peterson, David L Keefe, Elizabet Genis, Gabriele Fuchs, Ravikumar Balasubramanian, Paolo E Forni. J Neurosci 2020
9
100

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
Naresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, Jyoti Parkash, Cécile Espy, Corinne Fouveaut, Chrystel Leroy, Stéphanie Baron, Céline Campagne, Charlotte Vanacker,[...]. PLoS Genet 2012
122
100

Identification of ROBO1/2 and SCEL as candidate genes in Kallmann syndrome with emerging bioinformatic analysis.
Zuobin Zhu, Xiaoxiao Han, Ying Li, Conghui Han, Mengqiong Deng, Yuhao Zhang, Qing Shen, Yijuan Cao, Zhenbei Li, Xitao Wang,[...]. Endocrine 2020
3
100


Development of the neurons controlling fertility in humans: new insights from 3D imaging and transparent fetal brains.
Filippo Casoni, Samuel A Malone, Morgane Belle, Federico Luzzati, Francis Collier, Cecile Allet, Erik Hrabovszky, Sowmyalakshmi Rasika, Vincent Prevot, Alain Chédotal,[...]. Development 2016
63
100

GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing.
Luigi Maione, Andrew A Dwyer, Bruno Francou, Anne Guiochon-Mantel, Nadine Binart, Jérôme Bouligand, Jacques Young. Eur J Endocrinol 2018
71
100

A Balanced Translocation in Kallmann Syndrome Implicates a Long Noncoding RNA, RMST, as a GnRH Neuronal Regulator.
Maria Stamou, Shi-Yan Ng, Harrison Brand, Harold Wang, Lacey Plummer, Lyle Best, Steven Havlicek, Martin Hibberd, Chiea Chuen Khor, James Gusella,[...]. J Clin Endocrinol Metab 2020
8
100

Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.
Cheng Xu, Daniele Cassatella, Almer M van der Sloot, Richard Quinton, Michael Hauschild, Christian De Geyter, Christa Flück, Katrin Feller, Deborah Bartholdi, Attila Nemeth,[...]. Genet Med 2018
20
100

Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
Biagio Cangiano, Du Soon Swee, Richard Quinton, Marco Bonomi. Hum Genet 2021
37
100

WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome.
Yeon-Joo Kim, Daniel Ps Osborn, Ji-Young Lee, Masatake Araki, Kimi Araki, Timothy Mohun, Johanna Känsäkoski, Nina Brandstack, Hyun-Taek Kim, Francesc Miralles,[...]. EMBO Rep 2018
19
100

GnRH, anosmia and hypogonadotropic hypogonadism--where are we?
Paolo E Forni, Susan Wray. Front Neuroendocrinol 2015
67
100

Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a Nose.
Angela Delaney, Rita Volochayev, Brooke Meader, Janice Lee, Konstantinia Almpani, Germaine Y Noukelak, Jennifer Henkind, Laura Chalmers, Jennifer R Law, Kathleen A Williamson,[...]. J Clin Endocrinol Metab 2020
3
100

Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system.
Valerie F Sidhoum, Yee-Ming Chan, Margaret F Lippincott, Ravikumar Balasubramanian, Richard Quinton, Lacey Plummer, Andrew Dwyer, Nelly Pitteloud, Frances J Hayes, Janet E Hall,[...]. J Clin Endocrinol Metab 2014
77
100

Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
Sara Barraud, Brigitte Delemer, Céline Poirsier-Violle, Jérôme Bouligand, Jean-Claude Mérol, Florent Grange, Brigitte Higel-Chaufour, Bénédicte Decoudier, Mohamad Zalzali, Andrew A Dwyer,[...]. Neuroendocrinology 2021
8
100

Characterization of the human GnRH neuron developmental transcriptome using a GNRH1-TdTomato reporter line in human pluripotent stem cells.
Carina Lund, Venkatram Yellapragada, Sanna Vuoristo, Diego Balboa, Sara Trova, Cecile Allet, Nazli Eskici, Kristiina Pulli, Paolo Giacobini, Timo Tuuri,[...]. Dis Model Mech 2020
7
100

Clinical Management of Congenital Hypogonadotropic Hypogonadism.
Jacques Young, Cheng Xu, Georgios E Papadakis, James S Acierno, Luigi Maione, Johanna Hietamäki, Taneli Raivio, Nelly Pitteloud. Endocr Rev 2019
88
100

Semaphorin Signaling in GnRH Neurons: From Development to Disease.
Roberto Oleari, Antonella Lettieri, Alyssa Paganoni, Luca Zanieri, Anna Cariboni. Neuroendocrinology 2019
12
100

Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Samuel D Quaynor, Maggie E Bosley, Christina G Duckworth, Kelsey R Porter, Soo-Hyun Kim, Hyung-Goo Kim, Lynn P Chorich, Megan E Sullivan, Jeong-Hyeon Choi, Richard S Cameron,[...]. Mol Cell Endocrinol 2016
37
100

Psychological Aspects of Congenital Hypogonadotropic Hypogonadism.
Andrew A Dwyer, Neil Smith, Richard Quinton. Front Endocrinol (Lausanne) 2019
9
50

Postnatal Changes in Testicular Position Are Associated With IGF-I and Function of Sertoli and Leydig Cells.
Jaakko J Koskenniemi, Helena E Virtanen, Christine Wohlfahrt-Veje, Eliisa Löyttyniemi, Niels E Skakkebaek, Anders Juul, Anna-Maria Andersson, Katharina M Main, Jorma Toppari. J Clin Endocrinol Metab 2018
14
50

Next-generation sequencing of patients with congenital anosmia.
Anna Alkelai, Tsviya Olender, Catherine Dode, Sagit Shushan, Pavel Tatarskyy, Edna Furman-Haran, Valery Boyko, Ruth Gross-Isseroff, Matthew Halvorsen, Lior Greenbaum,[...]. Eur J Hum Genet 2017
7
50

Isolated GNRH deficiency: genotypic and phenotypic characteristics of the genetically heterogeneous Greek population.
M I Stamou, P Varnavas, M Kentrou, F Adamidou, A Voutetakis, J Jing, L Plummer, V Koika, N A Georgopoulos. Eur J Endocrinol 2017
7
50


Pregnancy in women with Kallmann's syndrome.
U Sungurtekin, I S Fraser, R P Shearman. Fertil Steril 1995
26
50

ANOS1: a unified nomenclature for Kallmann syndrome 1 gene (KAL1) and anosmin-1.
Fernando de Castro, Ruth Seal, Roberto Maggi. Brief Funct Genomics 2017
20
50


Transition in endocrinology: induction of puberty.
Leo Dunkel, Richard Quinton. Eur J Endocrinol 2014
50
50


Postnatal Testicular Activity in Healthy Boys and Boys With Cryptorchidism.
Tanja Kuiri-Hänninen, Jaakko Koskenniemi, Leo Dunkel, Jorma Toppari, Ulla Sankilampi. Front Endocrinol (Lausanne) 2019
14
50

GnRH and GnRH receptors in the pathophysiology of the human female reproductive system.
Roberto Maggi, Anna Maria Cariboni, Marina Montagnani Marelli, Roberta Manuela Moretti, Valentina Andrè, Monica Marzagalli, Patrizia Limonta. Hum Reprod Update 2016
66
50

A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism.
Rita Indirli, Biagio Cangiano, Eriselda Profka, Giovanna Mantovani, Luca Persani, Maura Arosio, Marco Bonomi, Emanuele Ferrante. Front Endocrinol (Lausanne) 2019
3
50


Reproductive endocrine phenotypes relating to CHD7 mutations in humans.
Ravikumar Balasubramanian, William F Crowley. Am J Med Genet C Semin Med Genet 2017
15
50

Correlations Among Genotype and Outcome in Chinese Male Patients With Congenital Hypogonadotropic Hypogonadism Under HCG Treatment.
Yinwei Chen, Taotao Sun, Yonghua Niu, Daoqi Wang, Zhiyong Xiong, Chuanzhou Li, Kang Liu, Youlan Qiu, Yi Sun, Jianan Gong,[...]. J Sex Med 2020
3
50

Histopathology of Unilateral Cryptorchidism.
Gilvydas Verkauskas, Dalius Malcius, Darius Dasevicius, Faruk Hadziselimovic. Pediatr Dev Pathol 2019
4
50

Replacement of Male Mini-Puberty.
Dimitrios T Papadimitriou, Dionysios Chrysis, Georgia Nyktari, George Zoupanos, Eleni Liakou, Anastasios Papadimitriou, George Mastorakos. J Endocr Soc 2019
14
50

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH).
Marco Bonomi, Valeria Vezzoli, Csilla Krausz, Fabiana Guizzardi, Silvia Vezzani, Manuela Simoni, Ivan Bassi, Paolo Duminuco, Natascia Di Iorgi, Claudia Giavoli,[...]. Eur J Endocrinol 2018
45
50

The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.
Nelly Pitteloud, Frances J Hayes, Paul A Boepple, Suzzunne DeCruz, Stephanie B Seminara, David T MacLaughlin, William F Crowley. J Clin Endocrinol Metab 2002
122
50

Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH.
Hélène Bry-Gauillard, Florence Larrat-Ledoux, Jean-Marc Levaillant, Nathalie Massin, Luigi Maione, Isabelle Beau, Nadine Binart, Philippe Chanson, Sylvie Brailly-Tabard, Janet E Hall,[...]. J Clin Endocrinol Metab 2017
28
50

Adherence to treatment in men with hypogonadotrophic hypogonadism.
Andrew A Dwyer, Jitske Tiemensma, Richard Quinton, Nelly Pitteloud, Diane Morin. Clin Endocrinol (Oxf) 2017
16
50

Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism.
Ja Hye Kim, Go Hun Seo, Gu-Hwan Kim, Juyoung Huh, Il Tae Hwang, Ja-Hyun Jang, Han-Wook Yoo, Jin-Ho Choi. Exp Clin Endocrinol Diabetes 2019
10
50

VEGF signalling controls GnRH neuron survival via NRP1 independently of KDR and blood vessels.
Anna Cariboni, Kathryn Davidson, Elena Dozio, Fani Memi, Quenten Schwarz, Fabio Stossi, John G Parnavelas, Christiana Ruhrberg. Development 2011
59
50

Gonadotropin-releasing hormone neuron development in vertebrates.
Cunming Duan, John Allard. Gen Comp Endocrinol 2020
6
50

Congenital hypogonadotropic hypogonadism: implications of absent mini-puberty.
Andrew A Dwyer, Channa N Jayasena, Richard Quinton. Minerva Endocrinol 2016
10
50



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.