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1.

Critical Assessment of Metagenome Interpretation: the second round of challenges.

Meyer, Fernando; Fritz, Adrian; Deng, Zhi-Luo; Koslicki, David; Lesker, Till Robin; Gurevich, Alexey; Robertson, Gary; Alser, Mohammed; Antipov, Dmitry; Beghini, Francesco; Bertrand, Denis; Brito, Jaqueline J; Brown, C Titus; Buchmann, Jan; Buluç, Aydin; Chen, Bo; Chikhi, Rayan; Clausen, Philip T L C; Cristian, Alexandru; Dabrowski, Piotr Wojciech; Darling, Aaron E; Egan, Rob; Eskin, Eleazar; Georganas, Evangelos; Goltsman, Eugene; Gray, Melissa A; Hansen, Lars Hestbjerg; Hofmeyr, Steven; Huang, Pingqin; Irber, Luiz; Jia, Huijue; Jørgensen, Tue Sparholt; Kieser, Silas D; Klemetsen, Terje; Kola, Axel; Kolmogorov, Mikhail; Korobeynikov, Anton; Kwan, Jason; LaPierre, Nathan; Lemaitre, Claire; Li, Chenhao; Limasset, Antoine; Malcher-Miranda, Fabio; Mangul, Serghei; Marcelino, Vanessa R; Marchet, Camille; Marijon, Pierre; Meleshko, Dmitry; Mende, Daniel R; Milanese, Alessio.

Nat Methods; 19(4): 429-440, 2022 04.

Artículo en Inglés | MEDLINE | ID: mdl-35396482

2.

Copeptin in the Diagnosis of Diabetes Insipidus.

Robertson, Gary L.

N Engl J Med; 379(18): 1784, 2018 11 01.

Artículo en Inglés | MEDLINE | ID: mdl-30382698

3.

Optimized model architectures for deep learning on genomic data.

Gündüz, Hüseyin Anil; Mreches, René; Moosbauer, Julia; Robertson, Gary; To, Xiao-Yin; Franzosa, Eric A; Huttenhower, Curtis; Rezaei, Mina; McHardy, Alice C; Bischl, Bernd; Münch, Philipp C; Binder, Martin.

Commun Biol; 7(1): 516, 2024 Apr 30.

Artículo en Inglés | MEDLINE | ID: mdl-38693292

4.

Temporal delays and individual variation in antidiuretic response to desmopressin.

Juul, Kristian Vinter; Erichsen, Lars; Robertson, Gary L.

Am J Physiol Renal Physiol; 304(3): F268-78, 2013 Feb 01.

Artículo en Inglés | MEDLINE | ID: mdl-23136002

5.

A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner.

Habiby, Reema; Bichet, Daniel G; Arthus, Marie-Francoise; Connaughton, Dervia; Shril, Shirlee; Mane, Shrikant; Majmundar, Amar J; Hildebrandt, Friedhelm; Robertson, Gary L.

J Clin Endocrinol Metab; 107(6): e2513-e2522, 2022 05 17.

Artículo en Inglés | MEDLINE | ID: mdl-35137152

6.

Differential diagnosis of familial diabetes insipidus.

Robertson, Gary L.

Handb Clin Neurol; 181: 239-248, 2021.

Artículo en Inglés | MEDLINE | ID: mdl-34238460

7.

Hypernatremic Hydrophobic Transient Adipsia Without Organic or Severe Psychiatric Disorder.

Rodriguez, Aleida; Fogelfeld, Leon; Robertson, Gary.

J Clin Endocrinol Metab; 104(11): 5427-5430, 2019 11 01.

Artículo en Inglés | MEDLINE | ID: mdl-31373657

8.

Author Correction: Optimized model architectures for deep learning on genomic data.

Gündüz, Hüseyin Anil; Mreches, René; Moosbauer, Julia; Robertson, Gary; To, Xiao-Yin; Franzosa, Eric A; Huttenhower, Curtis; Rezaei, Mina; McHardy, Alice C; Bischl, Bernd; Münch, Philipp C; Binder, Martin.

Commun Biol; 7(1): 625, 2024 May 23.

Artículo en Inglés | MEDLINE | ID: mdl-38783006

9.

Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene.

Faerch, Mia; Christensen, Jane H; Corydon, Thomas J; Kamperis, Konstantinos; de Zegher, Francis; Gregersen, Niels; Robertson, Gary L; Rittig, Søren.

Clin Endocrinol (Oxf); 68(3): 395-403, 2008 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-17941907

10.

The effects of mutating Tyr9 and Arg15 on the structure, stability, conformational dynamics and mechanism of GSTA3-3.

Robertson, Gary J; Stoychev, Stoyan H; Sayed, Yasien; Achilonu, Ikechukwu; Dirr, Heini W.

Biophys Chem; 224: 40-48, 2017 05.

Artículo en Inglés | MEDLINE | ID: mdl-28318907

11.

Diabetes insipidus: Differential diagnosis and management.

Robertson, Gary L.

Best Pract Res Clin Endocrinol Metab; 30(2): 205-18, 2016 03.

Artículo en Inglés | MEDLINE | ID: mdl-27156759

12.

Exposures of preschool children to chlorpyrifos and its degradation product 3,5,6-trichloro-2-pyridinol in their everyday environments.

Morgan, Marsha K; Sheldon, Linda S; Croghan, Carry W; Jones, Paul A; Robertson, Gary L; Chuang, Jane C; Wilson, Nancy K; Lyu, Christopher W.

J Expo Anal Environ Epidemiol; 15(4): 297-309, 2005 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-15367928

13.

Response to Letter to the Editor: "Hypernatremic Hydrophobic Transient Adipsia without Organic or Severe Psychiatric Disorder".

Rodriguez, Aleida; Fogelfeld, Leon; Robertson, Gary.

J Clin Endocrinol Metab; 105(3)2020 Mar 01.

Artículo en Inglés | MEDLINE | ID: mdl-31665336

14.

Autosomal dominant neurohypophyseal diabetes insipidus due to substitution of histidine for tyrosine(2) in the vasopressin moiety of the hormone precursor.

Rittig, Søren; Siggaard, Charlotte; Ozata, Metin; Yetkin, Ilhan; Gregersen, Niels; Pedersen, Erling B; Robertson, Gary L.

J Clin Endocrinol Metab; 87(7): 3351-5, 2002 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-12107248

15.

Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidus.

Christensen, Jane H; Siggaard, Charlotte; Corydon, Thomas J; Robertson, Gary L; Gregersen, Niels; Bolund, Lars; Rittig, Søren.

J Clin Endocrinol Metab; 89(9): 4521-31, 2004 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-15356057

16.

Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis.

Christensen, Jane H; Siggaard, Charlotte; Corydon, Thomas J; deSanctis, Luisa; Kovacs, Laszlo; Robertson, Gary L; Gregersen, Niels; Rittig, Søren.

Eur J Hum Genet; 12(1): 44-51, 2004 Jan.

Artículo en Inglés | MEDLINE | ID: mdl-14673472

17.

Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene.

Rutishauser, Jonas; Kopp, Peter; Gaskill, Mary Beth; Kotlar, Thomas J; Robertson, Gary L.

Eur J Endocrinol; 146(5): 649-56, 2002 May.

Artículo en Inglés | MEDLINE | ID: mdl-11980620

18.

Clinical review: Treatment of neurohypophyseal diabetes insipidus.

Oiso, Yutaka; Robertson, Gary L; Nørgaard, Jens Peter; Juul, Kristian Vinter.

J Clin Endocrinol Metab; 98(10): 3958-67, 2013 Oct.

Artículo en Inglés | MEDLINE | ID: mdl-23884783

19.

Vaptans for the treatment of hyponatremia.

Robertson, Gary L.

Nat Rev Endocrinol; 7(3): 151-61, 2011 Mar.

Artículo en Inglés | MEDLINE | ID: mdl-21283124

20.

Familial forms of diabetes insipidus: clinical and molecular characteristics.

Babey, Muriel; Kopp, Peter; Robertson, Gary L.

Nat Rev Endocrinol; 7(12): 701-14, 2011 Jul 05.

Artículo en Inglés | MEDLINE | ID: mdl-21727914

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Critical Assessment of Metagenome Interpretation: the second round of challenges.

Copeptin in the Diagnosis of Diabetes Insipidus.

Optimized model architectures for deep learning on genomic data.

Temporal delays and individual variation in antidiuretic response to desmopressin.

A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner.

Differential diagnosis of familial diabetes insipidus.

Hypernatremic Hydrophobic Transient Adipsia Without Organic or Severe Psychiatric Disorder.

Author Correction: Optimized model architectures for deep learning on genomic data.

Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene.

The effects of mutating Tyr9 and Arg15 on the structure, stability, conformational dynamics and mechanism of GSTA3-3.

Diabetes insipidus: Differential diagnosis and management.

Exposures of preschool children to chlorpyrifos and its degradation product 3,5,6-trichloro-2-pyridinol in their everyday environments.

Response to Letter to the Editor: "Hypernatremic Hydrophobic Transient Adipsia without Organic or Severe Psychiatric Disorder".

Autosomal dominant neurohypophyseal diabetes insipidus due to substitution of histidine for tyrosine(2) in the vasopressin moiety of the hormone precursor.

Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidus.

Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis.

Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene.

Clinical review: Treatment of neurohypophyseal diabetes insipidus.

Vaptans for the treatment of hyponatremia.

Familial forms of diabetes insipidus: clinical and molecular characteristics.