A citation-based method for searching scientific literature

Mark J McCabe, Carles Gaston-Massuet, Vaitsa Tziaferi, Louise C Gregory, Kyriaki S Alatzoglou, Massimo Signore, Eduardo Puelles, Dianne Gerrelli, I Sadaf Farooqi, Jamal Raza, Joanna Walker, Scott I Kavanaugh, Pei-San Tsai, Nelly Pitteloud, Juan-Pedro Martinez-Barbera, Mehul T Dattani. J Clin Endocrinol Metab 2011
Times Cited: 78







List of co-cited articles
1294 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.
Taneli Raivio, Magdalena Avbelj, Mark J McCabe, Christopher J Romero, Andrew A Dwyer, Johanna Tommiska, Gerasimos P Sykiotis, Louise C Gregory, Daniel Diaczok, Vaitsa Tziaferi,[...]. J Clin Endocrinol Metab 2012
87
35

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.
John Falardeau, Wilson C J Chung, Andrew Beenken, Taneli Raivio, Lacey Plummer, Yisrael Sidis, Elka E Jacobson-Dickman, Anna V Eliseenkova, Jinghong Ma, Andrew Dwyer,[...]. J Clin Invest 2008
245
33

Genetic regulation of pituitary gland development in human and mouse.
Daniel Kelberman, Karine Rizzoti, Robin Lovell-Badge, Iain C A F Robinson, Mehul T Dattani. Endocr Rev 2009
249
28

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.
M T Dattani, J P Martinez-Barbera, P Q Thomas, J M Brickman, R Gupta, I L Mårtensson, H Toresson, M Fox, J K Wales, P C Hindmarsh,[...]. Nat Genet 1998
499
24

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Catherine Dodé, Jacqueline Levilliers, Jean-Michel Dupont, Anne De Paepe, Nathalie Le Dû, Nadia Soussi-Yanicostas, Roney S Coimbra, Sedigheh Delmaghani, Sylvie Compain-Nouaille, Françoise Baverel,[...]. Nat Genet 2003
517
23

Genetic forms of hypopituitarism and their manifestation in the neonatal period.
Kyriaki S Alatzoglou, Mehul T Dattani. Early Hum Dev 2009
69
21

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3.
H Z Sheng, A B Zhadanov, B Mosinger, T Fujii, S Bertuzzi, A Grinberg, E J Lee, S P Huang, K A Mahon, H Westphal. Science 1996
359
19

Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans.
Daniel Kelberman, Karine Rizzoti, Ariel Avilion, Maria Bitner-Glindzicz, Stefano Cianfarani, Julie Collins, W Kling Chong, Jeremy M W Kirk, John C Achermann, Richard Ross,[...]. J Clin Invest 2006
213
19


Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephaly.
Marcela M França, Alexander A L Jorge, Luciani R S Carvalho, Everlayny F Costalonga, Gabriela A Vasques, Claudia C Leite, Berenice B Mendonca, Ivo J P Arnhold. J Clin Endocrinol Metab 2010
73
19

Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.
Mark J McCabe, Carles Gaston-Massuet, Louise C Gregory, Kyriaki S Alatzoglou, Vaitsa Tziaferi, Oualid Sbai, Philippe Rondard, Koh-hei Masumoto, Mamoru Nagano, Yasufumi Shigeyoshi,[...]. J Clin Endocrinol Metab 2013
38
36

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism.
Kathryn S Woods, Maria Cundall, James Turton, Karine Rizotti, Ameeta Mehta, Rodger Palmer, Jacqueline Wong, W K Chong, Mahmoud Al-Zyoud, Maryam El-Ali,[...]. Am J Hum Genet 2005
163
16

A Hypomorphic Allele in the FGF8 Gene Contributes to Holoprosencephaly and Is Allelic to Gonadotropin-Releasing Hormone Deficiency in Humans.
R F Arauz, B D Solomon, D E Pineda-Alvarez, A L Gropman, J A Parsons, E Roessler, M Muenke. Mol Syndromol 2010
39
33

Septo-optic dysplasia and other midline defects: the role of transcription factors: HESX1 and beyond.
Mark James McCabe, Kyriaki S Alatzoglou, Mehul T Dattani. Best Pract Res Clin Endocrinol Metab 2011
67
19

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
Catherine Dodé, Luis Teixeira, Jacqueline Levilliers, Corinne Fouveaut, Philippe Bouchard, Marie-Laure Kottler, James Lespinasse, Anne Lienhardt-Roussie, Michèle Mathieu, Alexandre Moerman,[...]. PLoS Genet 2006
288
16

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
238
16

Multistep control of pituitary organogenesis.
H Z Sheng, K Moriyama, T Yamashita, H Li, S S Potter, K A Mahon, H Westphal. Science 1997
288
15

Septo-optic dysplasia.
Emma A Webb, Mehul T Dattani. Eur J Hum Genet 2010
122
15

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Hichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, Lacey Plummer, Wilson Chung, Bihua Feng, Andrew Beenken, Jeff Clarke, Tune H Pers, Piotr Dworzynski,[...]. Am J Hum Genet 2013
154
15

Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers.
Elaine E Storm, Sonia Garel, Ugo Borello, Jean M Hebert, Salvador Martinez, Susan K McConnell, Gail R Martin, John L R Rubenstein. Development 2006
266
15

HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
David E G McNay, James P Turton, Daniel Kelberman, Kathryn S Woods, Raja Brauner, Anastasios Papadimitriou, Eberhard Keller, Alexandra Keller, Nele Haufs, Heiko Krude,[...]. J Clin Endocrinol Metab 2007
90
14

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.
Gerasimos P Sykiotis, Lacey Plummer, Virginia A Hughes, Margaret Au, Sadia Durrani, Sadhana Nayak-Young, Andrew A Dwyer, Richard Quinton, Janet E Hall, James F Gusella,[...]. Proc Natl Acad Sci U S A 2010
220
14

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.
I Netchine, M L Sobrier, H Krude, D Schnabel, M Maghnie, E Marcos, B Duriez, V Cacheux, A v Moers, M Goossens,[...]. Nat Genet 2000
222
14


Formation of Rathke's pouch requires dual induction from the diencephalon.
N Takuma, H Z Sheng, Y Furuta, J M Ward, K Sharma, B L Hogan, S L Pfaff, H Westphal, S Kimura, K A Mahon. Development 1998
222
14

Multistep signaling requirements for pituitary organogenesis in vivo.
M Treier, A S Gleiberman, S M O'Connell, D P Szeto, J A McMahon, A P McMahon, M G Rosenfeld. Genes Dev 1998
354
14

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.
Nelly Pitteloud, Richard Quinton, Simon Pearce, Taneli Raivio, James Acierno, Andrew Dwyer, Lacey Plummer, Virginia Hughes, Stephanie Seminara, Yu-Zhu Cheng,[...]. J Clin Invest 2007
262
12

Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
Nelly Pitteloud, Chengkang Zhang, Duarte Pignatelli, Jia-Da Li, Taneli Raivio, Lindsay W Cole, Lacey Plummer, Elka E Jacobson-Dickman, Pamela L Mellon, Qun-Yong Zhou,[...]. Proc Natl Acad Sci U S A 2007
186
12

A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins.
B Lamolet, A M Pulichino, T Lamonerie, Y Gauthier, T Brue, A Enjalbert, J Drouin. Cell 2001
353
12

PROKR2 variants in multiple hypopituitarism with pituitary stalk interruption.
Rachel Reynaud, Sujatha A Jayakody, Carine Monnier, Alexandru Saveanu, Jérome Bouligand, Anne-Marie Guedj, Gilbert Simonin, Pierre Lecomte, Anne Barlier, Philippe Rondard,[...]. J Clin Endocrinol Metab 2012
50
20

Three novel missense mutations within the LHX4 gene are associated with variable pituitary hormone deficiencies.
Roland W Pfaeffle, Chad S Hunter, Jesse J Savage, Mario Duran-Prado, Rachel D Mullen, Zachary P Neeb, Urs Eiholzer, Volker Hesse, Nadine G Haddad, Heike M Stobbe,[...]. J Clin Endocrinol Metab 2008
71
14

ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.
Emma A Webb, Angham AlMutair, Daniel Kelberman, Chiara Bacchelli, Estelle Chanudet, Francesco Lescai, Cynthia L Andoniadou, Abdul Banyan, Al Alsawaid, Muhammad T Alrifai,[...]. Brain 2013
40
25

OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary.
Toshihiro Tajima, Akira Ohtake, Masaya Hoshino, Shin Amemiya, Nozomu Sasaki, Katsura Ishizu, Kenji Fujieda. J Clin Endocrinol Metab 2009
63
14

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.
K Machinis, J Pantel, I Netchine, J Léger, O J Camand, M L Sobrier, F Dastot-Le Moal, P Duquesnoy, M Abitbol, P Czernichow,[...]. Am J Hum Genet 2001
174
11

Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency.
Frédéric Laumonnier, Nathalie Ronce, Ben C J Hamel, Paul Thomas, James Lespinasse, Martine Raynaud, Christine Paringaux, Hans Van Bokhoven, Vera Kalscheuer, Jean-Pierre Fryns,[...]. Am J Hum Genet 2002
214
11

FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development.
H Ohuchi, Y Hori, M Yamasaki, H Harada, K Sekine, S Kato, N Itoh. Biochem Biophys Res Commun 2000
463
11

Mutations in PROP1 cause familial combined pituitary hormone deficiency.
W Wu, J D Cogan, R W Pfäffle, J S Dasen, H Frisch, S M O'Connell, S E Flynn, M R Brown, P E Mullis, J S Parks,[...]. Nat Genet 1998
365
11

Role of PROP1 in pituitary gland growth.
Robert D Ward, Lori T Raetzman, Hoonkyo Suh, Brandon M Stone, Igor O Nasonkin, Sally A Camper. Mol Endocrinol 2005
128
11

Fibroblast growth factor signaling in the developing neuroendocrine hypothalamus.
Pei-San Tsai, Leah R Brooks, Johanna R Rochester, Scott I Kavanaugh, Wilson C J Chung. Front Neuroendocrinol 2011
28
32

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
Nicolas Simonis, Isabelle Migeotte, Nelle Lambert, Camille Perazzolo, Deepthi C de Silva, Boyan Dimitrov, Claudine Heinrichs, Sandra Janssens, Bronwyn Kerr, Geert Mortier,[...]. J Med Genet 2013
51
17

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.
Fernanda A Correa, Ericka B Trarbach, Cintia Tusset, Ana Claudia Latronico, Luciana R Montenegro, Luciani R Carvalho, Marcela M Franca, Aline P Otto, Everlayny F Costalonga, Vinicius N Brito,[...]. Endocr Connect 2015
26
34

Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation.
Roland W Pfaeffle, Jesse J Savage, Chad S Hunter, Christina Palme, Martina Ahlmann, Prasanna Kumar, Jaele Bellone, Eckhard Schoenau, Eckhard Korsch, Jürgen H Brämswig,[...]. J Clin Endocrinol Metab 2007
65
12


Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.
James P G Turton, Rachel Reynaud, Ameeta Mehta, John Torpiano, Alexandru Saveanu, Kathryn S Woods, Anatoly Tiulpakov, Vera Zdravkovic, Jill Hamilton, Simon Attard-Montalto,[...]. J Clin Endocrinol Metab 2005
73
10

A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.
Daniel Diaczok, Christopher Romero, Janice Zunich, Ian Marshall, Sally Radovick. J Clin Endocrinol Metab 2008
77
10

Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.
Anna Rajab, Daniel Kelberman, Sandra C P de Castro, Heike Biebermann, Hala Shaikh, Kerra Pearce, Catherine M Hall, Guftar Shaikh, Dianne Gerrelli, Annette Grueters,[...]. Hum Mol Genet 2008
58
13

Impaired FGF signaling contributes to cleft lip and palate.
Bridget M Riley, M Adela Mansilla, Jinghong Ma, Sandra Daack-Hirsch, Brion S Maher, Lisa M Raffensperger, Erilynn T Russo, Alexandre R Vieira, Catherine Dodé, Moosa Mohammadi,[...]. Proc Natl Acad Sci U S A 2007
195
10

Congenital hypopituitarism: clinical, molecular and neuroradiological correlates.
Ameeta Mehta, Peter C Hindmarsh, Hiten Mehta, James P G Turton, Isabelle Russell-Eggitt, David Taylor, W K Chong, Mehul T Dattani. Clin Endocrinol (Oxf) 2009
62
12

Nonsense mutations in FGF8 gene causing different degrees of human gonadotropin-releasing deficiency.
Ericka B Trarbach, Ana Paula Abreu, Leticia Ferreira Gontijo Silveira, Heraldo Mendes Garmes, Maria Tereza M Baptista, Milena Gurgel Teles, Elaine M F Costa, Moosa Mohammadi, Nelly Pitteloud, Berenice B Mendonca,[...]. J Clin Endocrinol Metab 2010
50
16

Homeodomain-mediated beta-catenin-dependent switching events dictate cell-lineage determination.
Lorin E Olson, Jessica Tollkuhn, Claudio Scafoglio, Anna Krones, Jie Zhang, Kenneth A Ohgi, Wei Wu, Makoto M Taketo, Rolf Kemler, Rudolf Grosschedl,[...]. Cell 2006
205
10


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.