PatriciaADonohoueMD

PubMed

• 18 citations
  A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development.
  Anu Bashamboo, Patricia A Donohoue, Eric Vilain, Sandra Rojo, Pierre Calvel, Sumudu N Seneviratne, Federica Buonocore, Hayk Barseghyan, Nathan Bingham, Jill A Rosenfel...> ;Human Molecular Genetics. 2016 Dec 1
• 34 citations
  A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development.
  Anu Bashamboo, Patricia A Donohoue, Eric Vilain, Sandra Rojo, Pierre Calvel, Sumudu N Seneviratne, Federica Buonocore, Hayk Barseghyan, Nathan Bingham, Jill A Rosenfel...> ;Human Molecular Genetics. 2016 Aug 15
• Contents Vol. 85, 2016
  Chiara De Leonibus, Peter E. Clayton, Francesco Chiarelli, Angelika Mohn, Stefania De Marco, Adam Stevens, Ewa Małecka-Tendera, Magdalena Olszanecka-Glinianowicz, Agni...> ;Hormone Research in Paediatrics. 2016 Jan 1
• 2 citations
  Impact of Age at Diagnosis and Hypothalamic Involvement on Body Mass Index Z-Score Change in Pediatric Brain Tumor Survivors
  Katie Strobel, Pippa Simpson, Patricia A. Donohoue, Selim Firat, Sachin Jogal> ;Hormone Research in Paediatrics. 2016 Jan 1
• 4 citations
  Recognition and treatment of concurrent active and neurodegenerative langerhans cell histiocytosis: a case report.
  Matthew J. Ehrhardt, Jeffrey S. Karst, Patricia A. Donohoue, Mohit Maheshwari, Kenneth L. McClain, Kristin Bingen, Michael E. Kelly> ;Journal of Pediatric Hematology/oncology. 2015 Jan 1
• 11 citations
  Perception and documentation of weight management practices in pediatric primary care.
  Gaya Chelvakumar, Laura Levin, Michele Polfuss, Susan Hovis, Patricia A. Donohoue, Amanda Kotowski> ;WMJ. 2014 Aug 1
• 9 citations
  Predictors of first-year growth response to a fixed-dose growth hormone treatment in children born small for gestational age: results of an open-label, multicenter tri...
  Robert Rapaport, Paul Saenger, Michael Wajnrajch, Bruce A. Boston, Mauri Carakushansky, Steven D. Chernausek, Pamela A. Clark, Jay Cohen, Deborah Counts, Patricia A. D...> ;Journal of Pediatric Endocrinology & Metabolism. 2008 Jan 1
• 135 citations
  Summary of Consensus Statement on Intersex Disorders and Their Management
  Christopher P. Houk, Ieuan A. Hughes, S Faisal Ahmed, Peter A. Lee, Olaf Hiort, Eric Vilain, Melissa Hines, Sheri A. Berenbaum, Ken Copeland, Patricia A. Donohoue, Lau...> ;Pediatrics. 2006 Aug 1
• 81 citations
  Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations
  Sophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, M. Gueydan, Anne Barlier, Michel David, Marc Nicolino, Georges Malpuech, Pierre Déchelotte, Cheri Deal, Guy ...> ;The Journal of Clinical Endocrinology and Metabolism. 2005 Mar 1
• 2 citations
  A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations.
  Sophie Vallette-Kasic, Anne-Marie Pulichino, M. Gueydan, Anne Barlier, Michel David, Georges Malpuech, Cheri Deal, G. Van Vliet, M de Vroede, Felix G. Riepe, Carl-Joac...> ;Endocrine Research. 2004 Nov 1
• 34 citations
  Deletion of codons 88-92 of the melanocortin-4 receptor gene: a novel deleterious mutation in an obese female.
  Patricia A. Donohoue, Ya-Xiong Tao, Malia M. Collins, Giles S.H. Yeo, Stephen O'Rahilly, Deborah L. Segaloff> ;The Journal of Clinical Endocrinology and Metabolism. 2003 Dec 1
• 88 citations
  A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference.
  Moonseong Heo, Rudolph L. Leibel, Kevin R. Fontaine, Bert B. Boyer, W. K. Chung, M. Koulu, M. K. Karvonen, U. Pesonen, Aila Rissanen, Markku Laakso, M. I. J. Uusitupa,...> ;International Journal of Obesity and Related Metabolic Disorders. 2002 May 1
• 50 citations
  Pooling analysis of genetic data: the association of leptin receptor (LEPR) polymorphisms with variables related to human adiposity.
  Moonseong Heo, Rudolph L. Leibel, Bert B. Boyer, Wendy K. Chung, Markku Koulu, Matti K. Karvonen, Ullamari Pesonen, Aila Rissanen, Markku Laakso, M. I. J. Uusitupa, Yv...> ;Genetics. 2001 Nov 1
• 39 citations
  Sympathetic inhibition, leptin, and uncoupling protein subtype expression in normal fasting rats.
  William I. Sivitz, Brian D. Fink, Donald A. Morgan, J. M. Fox, Patricia A. Donohoue, William G. Haynes> ;The American Journal of Physiology. 1999 Oct 1
• 34 citations
  Premature sexual development in individuals with neurodevelopmental disabilities
  Siraj U. Siddiqi, Don C Van Dyke, Patricia A. Donohoue, Dianne M. McBrien> ;Developmental Medicine and Child Neurology. 1999 Jun 1
• 84 citations
  Fasting and leptin modulate adipose and muscle uncoupling protein: divergent effects between messenger ribonucleic acid and protein expression.
  William I. Sivitz, Brian D. Fink, Patricia A. Donohoue> ;Endocrinology. 1999 Apr 1
• 130 citations
  Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita
  Anne T. Reutens, John C. Achermann, Masafumi Ito, M Ito, Wen Xia Gu, Reema L. Habiby, Patricia A. Donohoue, Songya Pang, Peter C. Hindmarsh, J. Larry Jameson> ;The Journal of Clinical Endocrinology and Metabolism. 1999 Feb 1
• 56 citations
  Plasma leptin in diabetic and insulin-treated diabetic and normal rats
  William I. Sivitz, Susan A. Walsh, Donald A. Morgan, Patricia A. Donohoue, William G. Haynes, Rudy L. Leibel> ;Metabolism. 1998 May 1
• 11 citations
  E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
  Linda J. Kirby-Keyser, Craig C. Porter, Patricia A. Donohoue> ;Human Mutation. 1997 Jan 1
• 5 citations
  Phenotypic evolution of classic 21-hydroxylase deficiency
  William H. Hoffman, Myung Y. Shin, Patricia A. Donohoue, Sandra W. Helman, Stephanie L. Brown, George Rosculet, Virendra B. Mahesh> ;Clinical Endocrinology. 1996 Jul 1
• 13 citations
  Linkage of congenital isolated adrenocorticotropic hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms
  Jennifer H. Kyllo, Malia M. Collins, Kimberly L. Vetter, Leona Cuttler, Robert L. Rosenfield, Patricia A. Donohoue> ;American Journal of Medical Genetics. 1996 Mar 29
• 30 citations
  Rat Adipose ob mRNA Levels in States of Altered Circulating Glucose and Insulin
  William I. Sivitz, Holly L. Bailey, Patricia A. Donohoue> ;Biochemical and Biophysical Research Communications. 1996 Mar 27
• 12 citations
  Constitutive human steroid 21-hydroxylase promoter gene and pseudogene activity in steroidogenic and nonsteroidogenic cells with the luciferase gene as a reporter.
  Jennifer H. Kyllo, Malia M. Collins, Patricia A. Donohoue> ;Endocrine Research. 1995 Nov 1
• 9 citations
  The HLA‐A3, Cw6, B47, DR7 extended haplotypes in salt losing 21‐hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with...
  Patricia A. Donohoue, Lisbeth A. Guethlein, Malia M. Collins, C Van Dop, Claude J. Migeon, Wilma B. Bias, B.J. Schmeckpeper> ;Tissue Antigens. 1995 Sep 1
• 11 citations
  A new way to seal glass plates for denaturing gradient gel electrophoresis.
  Kyllo Jh, Linda J. Kirby-Keyser, Patricia A. Donohoue, Craig C. Porter> ;Biotechniques. 1994 May 1
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Journal Articles

• Impact of age at diagnosis and hypothalamic involvement on body mass index z-score change in pediatric brain tumor survivors  
  Strobel K, Simpson P, Donohoue PA, Firat S, Jogal S, Hormone Research in Paediatrics, 1/1/2016
• Recognition and treatment of concurrent active and neurodegenerative Langerhans Cell Histiocytosis: a case report  
  Ehrhardt MJ, Karst J, Donohoue PA, Maheshwari M, McClain KL, Bingen K, Kelly ME, J Pediatr Hematol Oncol, 1/1/2015
• Perception and Documentation of Weight Management Practices in Pediatric Primary Care  
  Chelvakumar C, Levin L, Polfuss M, Hovis S, Donohoue P, Kotowski A, Wisconsin Medical Journal, 1/1/2014
• Predictors of first-year growth response to a fixed-dose growth hormone treatment in children born small for gestational age: results of an open-label, multicenter tri...  
  Rapaport R, Saenger P, Wajnrajch MP, and the Pfizer SGA Collaborative Study Group, J Pediatr Endocrinol Metab, 1/1/2008
• Consensus Statement on Management of Intersex Disorders  
  Hughes IA, Houk C, Ahmed SF, Lee PA and the LWPES/ESPE Consensus Group, Pediatrics, 1/1/2006
• Consensus Statement on Management of Intersex Disorders  
  Hughes IA, Houk C, Ahmed SF, Lee PA and the LWPES/ESPE Consensus Group, Archives of Disease in Childhood, 1/1/2006
• Consensus Statement on Management of Intersex Disorders  
  Hughes IA, Houk C, Ahmed SF, Lee PA and the LWPES/ESPE Consensus Group, Journal of Pediatric Urology (UK), 1/1/2006
• Congenital isolated ACTH deficiency, an underestimated cause of neonatal death, explained by TPIT mutations  
  Vallette-Kasic S., Pulichino A.M., Gueydan M., Barlier A., David M., Nicolino M., Malpuech G., Déchelotte P., Deal C., Van Vliet G., De Vroede M., Riepe F.G., Partsch ..., J Clin Endocrinol Metab, 1/1/2005
• Deep venous thrombosis and Turner syndrome  
  Jobe S., Donohoue P.A., Di Paolo G, Journal of Pediatric Hematology/Oncology, 1/1/2004
• A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations  
  Vallette-Kasic S., Pulichino A.M., Gueydan M., Barlier A., David M., Malpuech G., Deal C., Van Vliet G., De Vroede M., Riepe F., Partsch C-J., Sippell W., Berberoglu M..., Endocrine Research, 1/1/2004
• A meta-analytic investigation of linkage and association of common leptin receptor (LEPR) polymorphisms with body mass index and waist circumference  
  Heo M., Leibel R.L., Fontaine K.R., Boyer B.B., Chung W.K., Koulu M., Karvonen M.K., Pesonen U., Rissanen A., Laakso M., Uusitupa M.I.J, Chagnon Y., Bouchard C., Donoh..., International Journal of Obesity, 1/1/2002
• Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology  
  Joint LWPES/ESPE CAH Working Group, J Clin Endocrinol Metab, 1/1/2002
• Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society Endocrinology  
  ESPE/LWPES CAH Working Group, Hormone Research, 1/1/2002
• Pooling analysis of genetic data: an example of the association of LEPR polymorphisms with variables related to human adiposity  
  Heo M., Leibel R.L., Boyer B.B., Chung W.K., Koulu M., Karvonen M., Pesonen U., Rissanen A., Laakso M., Uusitupa M., Chagnon Y., Bouchard C., Donohoue P.A., Burns T.L...., Genetics, 1/1/2001
• Clinical and functional effects of mutations in the Dax-1 gene in patients with phenotypically disparate presentations of adrenal hypoplasia congenita (AHC)  
  Reutens A.T., Achermann J.C., Ito M., Ito M., Gu W-X., Habiby R.L., Donohoue P.A., Pang S., Hindmarsh P.C., Jameson J.L., J. Clin. Endocrinol. Metab., 1/1/1999
• Fasting and leptin modulate adipose and muscle uncoupling protein: divergent effects between mRNA and protein expression  
  Sivitz W.I., Fink, B.D., Donohoue, P.A., Endocrinology, 1/1/1999
• Premature sexual development in individuals with developmental disabilities  
  Siddiqi S.U., Donohoue P.A., Van Dyke D., McBrien, D.M., Developmental Medicine and Child Neurology, 1/1/1999
• Sympathetic inhibition, leptin, and uncoupling protein subtype expression in normal fasting rats  
  Sivitz W.I., Fink B.D., Morgan D.A., Fox J.M., Donohoue P.A., Haynes W.G., Am J. Physiol., 1/1/1999
• Plasma leptin levels in diabetic and insulin-treated diabetic and normal rats  
  Sivitz W.I., Walsh S., Donohoue P.A., Leibel R.L., Metabolism, 1/1/1998
• E380D: A novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency  
  Kirby-Keyser L., Porter C., Donohoue P.A., Human Mutation, 1/1/1997
• Linkage of congenital isolated adrenocorticotropin hormone deficiency to the corticotropin releasing hormone locus using simple sequence repeat polymorphisms  
  Kyllo J.H., Collins M.M., Vetter K.L., Cuttler L., Rosenfield R.L., Donohoue P.A., Am. J. Med. Genet., 1/1/1996
• Rat adipose ob mRNA levels in states of altered circulating glucose and insulin  
  Sivitz W.I., Bailey H.L., Donohoue P.A., Biochem. Biophys. Res. Commun., 1/1/1996
• Phenotypic evolution of classic 21-hydroxylase deficiency  
  Shin M.Y., Hoffman W.H., Donohoue P.A., Helman S.W., Brown S.L., Rosculet G., Mahesh V.B., Clinical Endocrinology, 1/1/1996
• The HLA-A3, Cw6, Bw47, DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: Identical MHC class I antigens and class II alleles...  
  Donohoue P.A., Guethlein L., Collins M.M., Van Dop C., Migeon C.J., Bias W.B., Schmeckpeper B.J., Tissue Antigens, 1/1/1995
• Constitutive human steroid 21-hydroxylase promoter activity in nonsteroidogenic cells as assessed with the luciferase gene as a reporter  
  Kyllo J.H., Collins M.M., Donohoue P.A., Endocrine Research, 1/1/1995
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Books/Book Chapters

• Principles and Practice of Medical Genetics 
  Chapter: Disorders of the Body Mass 
  Donohoue PA, Ali OEditors: Rimoin D et al.Elsevier, Inc.Edition 6th,2013
• Nelson's Textbook of Pediatrics 
  Chapter: Hypofunction of the ovaries. 
  Kansra A and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Hypergonadotropic hypogonadism in females. 
  Kansra A and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Hypogonadotropic Hypogonadism in females. 
  Kansra A and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Pseudoprecocity due to lesions of the ovary. 
  Kansra A and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Hypofunction of the testes. 
  Ali O and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Hypergonadotropic and hypogonadotropic hypogonadism in males. 
  Ali O and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Pseudoprecocity secondary to testicular tumors. 
  Ali O and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Gynecomastia 
  Ali O and Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Development and function of the gonads. 
  Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: Disorders of Sex Development (DSD) overview. 
  Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Nelson's Textbook of Pediatrics 
  Chapter: 46XX DSD, 46 XY DSD, ovotesticular DSD. 
  Donohoue PAEditors: Kliegman RM et al.Elsevier, Inc.Edition 19th,2012
• Pediatric Practice: Endocrinology 
  Chapter: Adrenal Disorders 
  Donohoue P.A.Editors: Kappy M, Allen D, Geffner M.McGraw Hill, New York2010
• Oski's Pediatrics: Principles & Practice 
  Chapter: Diseases of the Endocrine System: Adrenal cortex and Adrenal Medulla 
  Page 2133 - 2145Donohoue P.A.Editors: McMillan J., Feigin R.D., DeAngelis C.D., Jones, Jr, M.D..J.B. Lippincott Company Pub., PhiladelphiaEdition 4th,2006
• Emery & Rimoin's Principles and Practice of Medical Genetics 
  Chapter: Disorders of the Body Mass 
  Donohoue P.A.Editors: Rimoin D.L., Connor J.M.C., Pyeritz R.E., and Korf B.R..Harcourt Health Sciences, EdinburghEdition 5th,2006
• Prevention of Cardiovascular Disease 
  Chapter: Epidemiology of Childhood Overweight and Obesity 
  Burns T.L., Peyser P., and Donohoue P.A.Editors: Lauer R.M., Burns T.L., and Daniels S..Oxford University Press, Oxford2005
• Principles and Practice of Pediatric Endocrinology 
  Chapter: Adrenal Disorders 
  Page 357 - 486Donohoue P.A.Editors: Kappe M.S., Allen D., Geffner M..Charles C. Thomas, Springfield2005
• Nelson Textbook of Pediatrics 
  Chapter: Obesity 
  Page 173 - 177Donohoue P.A.Editors: Behrman R., Kliegman R.M., and Jenson H.B...B. Saunders Co., OrlandoEdition 17th,2004
• Saunders Manual of Pediatric Practice 
  Chapter: Ambiguous Genitalia. 
  Page 872 - 875Donohoue P.A., Saenger, P.H.Editors: Finberg L, Kleinman R.Harcourt Health Sciences Companies, PhiladelphiaEdition 2nd,2002
• Principles & Practice of Pediatrics 
  Chapter: Endocrine abnormalities: the adrenal cortex and the adrenal medulla. 
  Donohoue P.A.Editors: Oski F.A..J.B. Lippencott Company, Pub., Philadelphia2001
• Emery & Rimoin's Principles and Practice of Medical Genetics 
  Chapter: Disorders of the Body Mass. 
  Page 2385 - 2404Donohoue P.A.Editors: Rimoin D.L., Connor J.M.C., Pyeritz R.E., and Korf B.R..Harcourt Health Sciences, EdinburghEdition 4th,2001
• Oski's Pediatrics: Principles & Practice 
  Chapter: Endocrine abnormalities: the thyroid. 
  Page 1803 - 1812Donohoue P.A.Editors: DeAngelis C.D., Feigin R.D., McMillan J., Warshaw J.B..J.B. Lippincott Company Pub., PhiladelphiaEdition 3rd,1999
• Oski's Pediatrics: Principles & Practice 
  Chapter: Endocrine abnormalities: the adrenal cortex and the adrenal medulla. 
  Page 1812 - 1822Donohoue P.A.Editors: DeAngelis C.D., Feigin R.D., McMillan J., Warshaw J.B..J.B. Lippincott Company Pub., PhiladelphiaEdition 3rd,1999
• The Metabolic and Molecular Bases of Inherited Disease 
  Chapter: Congenital adrenal hyperplasia. 
  Page 2929 - 2963Donohoue P.A., Parker K.L., Migeon C.J.Editors: Schriver C.R., et al.McGraw-Hill Publishing Co., New YorkEdition 7th,1995
• Wilkins' Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence 
  Chapter: Adrenal disorders. 
  Page 717 - 856Migeon C.J., Donohoue P.A.Editors: Kappy M.S., et al.Charles C. Thomas Pub., SpringfieldEdition 4th,1994
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Abstracts/Posters

• Impact of age at diagnosis on obesity in pediatric brain tumor survivors.
  Strobel K, Simpson P, Donohoue P, Firat S, Jogal S, International Society for Pediatric Hematology-Oncology, Toronto, Ontario, Canada, 1/1/2014
• Impact of age at diagnosis on obesity in pediatric brain tumor survivors.
  Strobel K, Simpson P, Donohoue P, Firat S, Jogal S, Society of Neuro-Oncology, Miami, FL, 1/1/2014
• Assessment of overweight/obesity in pediatric care practices.
  Chelvakumar G, Levin L, Kotowski A, Polfuss M, Hovis S, Vidmar A, Donohoue P, Pediatric Academic Societies Annual Meeting, Washington, DC, 1/1/2013
• Management of feminizing testis tumors in prepubertal boys.
  Benabdallah JO, Donohoue P, Balcom AH, Wisconsin Urological Society, The Dells, WI, 1/1/2013
• Women's Faculty Council project on back-up care benefits.
  Sahoo D, Donohoue PA, et al, American Association of Medical Colleges (AAMC) Annual Meeting, 1/1/2012
• Analysis of PROP1 transcriptional regulatory sequences in patients with hypopituitarism.
  Carvalho L., Ward R.D.. Davis S.W., Nishi M.Y., Cogan J.D., Donohoue PA., Rhodes S., Walvoord E.C., Lyons R.H., Phillips J.A., Arnhold I.J.P., Mendonca B.B., Camper S.A., The Endocrine Society, 1/1/2007
• Transmission Disequilibrium of genetic loci in Muscatine, Iowa children within the upper decile of BMI.
  Burns T.L., Donohoue P.A., Chung W.K., Leibel R.L., American Heart Association, 1/1/2004
• Congenital isolated ACTH deficiency, an underestimated cause of neonatal death, explained by TPIT mutations.
  Vallette-Kasic S., Pulichino A.M., Gueydan M., Barlier A., David M., Malpuech G., Deal C., Van Vliet G., De Vroede M., Riepe F.G., Partsch C-J., Sippell W.G., Berberog..., The Endocrine Society, 1/1/2004
• The association of genotype, physical activity, and their interaction on age/gender adjusted body mass index (BMI): The Muscatine Study.
  Donohoue P.A., Mendoza M.B., Collins, M.M., Hamilton, W.L., Burns, T.L., Pediatric Research, 1/1/2001
• Lys656Asn variant of the leptin receptor gene (LEPR) and the Beta-3 Adrenergic receptor (B3AR) gene linked to body mass index in humans: The Muscatine Study.
  Donohoue P.A., Burns T.L., Mendoza M.C.B., Chung W.K., Leibel R.L., Pediatr Res, 1/1/2000
• Novel mutation of the human melanocortin-4 receptor (MC4-R) in an obese female.
  Donohoue P.A., Collins M.M., The Endocrine Society, 1/1/2000
• Multinodular goiter in multiple female family members.
  Tansey M.J., Donohoue P.A., The Endocrine Society, 1/1/2000
• Prevalence and effect of the N363S glucocorticoid receptor polymorphism in body mass index in an obese pediatric population.
  Tansey M.J., Hoffman R.P., Donohoue P.A., Journal of Investigative Medicine, 1/1/2000
• Polymorphism of exon 12 of the leptin receptor gene (LEPR) and the Beta-3 Adrenergic receptor (B3AR) gene linked to body mass index in humans: The Muscatine Study.
  Donohoue P.A., Burns T.L., Chung W.K., Leibel R.L., Journal of Investigative Medicine, 1/1/1999
• A preliminary meta-analysis of the association of LEPR polymorphisms with anthropometric variables.
  Heo M, Leibel R.L., Boyer B.B., Chung W.K., Koulu M., Karvonen M., Pesonen U., Rissanen A., Laasko M., Uusitupa M., Chagnon Y., Bouchard C., Donohoue PA, Burns T.L., S..., National Association for the Study of Obesity, 1/1/1999
• The Kenny Syndrome: Hypoparathyroidism caused by hypomagnesemia, and positive growth response to growth hormone treatment (report of a case).
  Donohoue P.A., Judisch F.S., Pediatric Research, 1/1/1998
• The leptin and leptin receptor loci contribute to variability in body size determinants in a large unselected population from Muscatine, Iowa.
  Donohoue P.A., Burns T.L., Leibel, R.L., The Endocrine Society, 1/1/1998
• Loci linked to quantitative body size measures from a genomic scan: The Muscatine Study.
  Burns, T.L., Donohoue, P.A., Lauer, R.M., Mendoza, M.C., Nishimura, D.Y., Sheffield, V.C., Circulation, 1/1/1998
• Normal and CAH mutant 21-hydroxylase promoter activities differ in an in vitro luciferase reporter assay.
  Donohoue P.A., Wedell A., Hormone Research, Joint Meeting of the European Society for Paediatric Endocrinology and Lawson Wilkins Pediatric Endocrine Society, 1/1/1997
• Normal and congenital adrenal hyperplasia (CAH) mutant 21-hydroxylase promoter activities differ in reporter assay.
  Donohoue P.A., Wedell A., Kyllo J.H., Collins M.M., The Endocrine Society, 1/1/1997
• Adipose Ob mRNA levels in states of altered circulating glucose and insulin.
  Sivitz W.I., Bailey H., Donohoue P.A., Diabetes, 1/1/1996
• Plasma leptin levels in diabetic and insulin-treated diabetic rats.
  Sivitz, W.I., Donohoue P.A., Leibel R.L., Journal of Investigative Medicine, 1/1/1996
• Identification of obesity genes using sib-pair linkage analysis: The Muscatine Study.
  Burns T.L., Donohoue P.A., Leibel R., Circulation, American Heart Association 35th Annual Conference on Cardiovascular Disease Epidemiology and Prevention, 1/1/1995
• A polymorphism of D1S85 (VC85) is associated with obesity in the population of Muscatine, Iowa.
  Morgan M.M., Donohoue P.A., Burns T.L., Zirkel T., Becker G.C., Power-Kehoe L., Chung W.K., Chua S.C., Jr., and Leibel R.L., The Endocrine Society, 1/1/1995
• Human steroid 21-hydroxylase promoter activity is greater than 21-hydroxylase pseudogene promoter activity in steroidogenic cells.
  Kyllo J.H., Collins M.M., Donohoue P.A., The Endocrine Society, 1/1/1995
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Lectures

• Steroid review/Adrenal insufficiency. 
  Medical College of Wisconsin, 2008-2016 - 1/1/2017
• Congenital adrenal hyperplasia. 
  Medical College of Wisconsin, 2008-2016 - 1/1/2017
• Disorders of Sex Development 
  Medical College of Wisconsin, 2008-2016 - 1/1/2017
• Prenatal Treatment of CAH 
  Medical College of Wisconsin, - 1/1/2017
• Endocrine Effects of Brain Tumors 
  Children's Hospital of Wisconsin - 1/1/2015
• Disorders of Sex Development: Changing Approaches to Management 
  1/1/2015
• Topic Symposium: Assessment of Adrenal Function in the Neonate 
  1/1/2014
• Controversies in Management of Congenital Adrenal Hyperplasia 
  Kansas City, MO - 1/1/2014
• Growth Hormone Therapy in 2014: Benefits, Risks, and Considerations in Patients with Neoplastic Disease 
  1/1/2014
• Adrenal insufficiency. 
  Medical College of Wisconsin, - 1/1/2013
• Adrenal Disorders 
  Medical College of Wisconsin, - 1/1/2013
• Genetics and Epidemiology of Obesity 
  Medical College of Wisconsin, - 1/1/2011
• Optimal Management of Children with Brain Tumors: Short and Long Term Endocrine Consequences of Brain Tumors and their Treatment 
  Medical College of Wisconsin, - 1/1/2011
• Update on Congenital Adrenal Hyperplasia 
  Medical College of Wisconsin, - 1/1/2011
• Case discussions. 
  Menomonee Falls, WI - 1/1/2011
• Negotiating the Academic Maze: Finding the Door to the Leadership Table 
  1/1/2011
• Steroid Dosing in the ICU 
  1/1/2010
• Adrenal function in the critically ill. 
  1/1/2010
• Congenital Adrenal Hyperplasia in Adults 
  Menomonee Falls, WI - 1/1/2009
• Thyroid Conditions in Childhood 
  Grayslake, IL - 1/1/2008
• Childhood Obesity 
  1/1/2007
• Adrenal Function in Critically Ill 
  University Of Missouri, Columbia - 1/1/2007
• Prader Willi Syndrome: Care of the Adult Patient 
  University of Iowa - 1/1/2007
• Molecular Biology Techniques 
  University of Iowa - 1/1/2007
• Topic Symposium: Role or No Role for prenatal diagnosis and testing in CAH. 
  1/1/2006
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Other

• Causes and clinical manifestations of primary adrenal insufficiency in children. 
  Donohoue PA, UpToDate
  www.uptodate.com
  Waltham, MA - 1/1/2016
• Causes and clinical manifestations of secondary (pituitary) and tertiary (hypothalamic) adrenal insufficiency in children. 
  Donohoue PA, UpToDate
  www.uptodate.com
  Waltham, MA - 1/1/2016
• Diagnosis of adrenal insufficiency in children. 
  Donohoue PA, UpToDate
  www.uptodate.com
  Waltham, MA - 1/1/2016
• Treatment of adrenal insufficiency in children. 
  Donohoue PA, UpToDate
  www.uptodate.com
  Waltham, MA - 1/1/2016
• Disease-oriented testing. 
  Donohoue PA, Critical Inquiry Series (a project of University Pathology Consortium, L.L.C.; Sims K., M.D., CEO)
  www.criticalinquiry.com
  1/1/2004
• Congenital adrenal hyperplasia: 21-hydroxylase deficiency. 
  Donohoue PA, Critical Inquiry Series (a project of University Pathology Consortium, L.L.C.; Sims K., M.D., CEO)
  www.criticalinquiry.com
  1/1/2004
• Adrenogenital Syndromes. 
  Donohoue PA, Critical Inquiry Series (a project of University Pathology Consortium, L.L.C.; Sims K., M.D., CEO)
  www.criticalinquiry.com
  1/1/2004
• Congenital Adrenal Hyperplasia. 
  Donohoue, P.A., International Symposium on A Current Review of Pediatric Endocrinology (Course Syllabus, Serono Pub.
  1/1/1999
• Fertility and genitourinary disorders: Fertility in patients with congenital adrenal hyperplasia due to the 21-hydroxylase deficiency. 
  Migeon C.J., Donohoue P.A., Dialogues in Pediatric Urology
  1/1/1990
• Causes and clinical manifestations of central adrenal insufficiency in children 
  Donohoue PA
  http://www.uptodate.com/contents/causes-and-clinical-manifestations-of-central-adrenal-insufficiency
  UpToDate, Wolters Kluwer Health - 2012-07-03
• Causes and clinical manifestations of primary adrenal insufficiency in children 
  Donohoue PA
  http://www.uptodate.com/contents/causes-and-clinical-manifestations-of-primary-adrenal-insufficiency
  UpToDate, Wolters Kluwer Health - 2012-03-01
• Diagnosis of adrenal insufficiency in children 
  Donohoue PA
  http://www.uptodate.com/contents/diagnosis-of-adrenal-insufficiency-in-children
  UpToDate, Wolters Kluwer Health - 2013-01-09
• Treatment of adrenal insufficiency in children 
  Donohoue PA
  http://www.uptodate.com/contents/treatment-of-adrenal-insufficiency-in-children
  UpToDate, Wolters Kluwer Health - 2012-08-30
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