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F. Rohr · SciRah

Researcher profile · Semantic Scholar

F. Rohr

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F. Rohr — researcher profile on SciRah

h-index: 28
Works: 70
Citations: 2,662

Most-cited papers

Phenylketonuria Scientific Review Conference: state of the science and future research needs.
Kathryn M. Camp, M. Parisi, P. Acosta, G. Berry +58 more
2014Molecular Genetics and Metabolism245 citations
Semantic Scholar
Recommendations for the nutrition management of phenylalanine hydroxylase deficiency
Rani H. Singh, F. Rohr, D. Frazier, A. Cunningham +8 more
2014Genetics in Medicine207 citations Open access
Semantic Scholar
Nutrition management guideline for maple syrup urine disease: an evidence- and consensus-based approach.
D. Frazier, Courtney Allgeier, C. Homer, B. Marriage +5 more
2014Molecular Genetics and Metabolism191 citations Open access
Semantic Scholar
Adherence to clinic recommendations among patients with phenylketonuria in the United States.
E. Jurecki, S. Cederbaum, J. Kopesky, K. Perry +5 more
2017Molecular Genetics and Metabolism178 citations Open access
Semantic Scholar
The Adult Galactosemic Phenotype
S. Waisbren, Nancy L. Potter, C. Gordon, R. Green +28 more
2011Journal of Inherited Metabolic Disease165 citations Open access
Semantic Scholar
Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach.
Rani H. Singh, A. Cunningham, S. Mofidi, T. Douglas +12 more
2016Molecular Genetics and Metabolism105 citations
Semantic Scholar
Prevalence of comorbid conditions among adult patients diagnosed with phenylketonuria.
B. Burton, K. B. Jones, S. Cederbaum, F. Rohr +7 more
2018Molecular Genetics and Metabolism90 citations Open access
Semantic Scholar
Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial12
D. Ney, Bridget M. Stroup, M. Clayton, S. Murali +3 more
2016American Journal of Clinical Nutrition74 citations Open access
Semantic Scholar
Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
G. Cox, M. Souri, T. Aoyama, S. Rockenmacher +4 more
1998Jornal de Pediatria73 citations
Semantic Scholar
Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria
N. Longo, D. Dimmock, H. Levy, K. Viau +13 more
2018Genetics in Medicine71 citations Open access
Semantic Scholar
International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria.
A. Muntau, Darius J. Adams, A. Bélanger-Quintana, T. Bushueva +14 more
2019Molecular Genetics and Metabolism67 citations Open access
Semantic Scholar
Nutrition management guideline for very-long chain acyl-CoA dehydrogenase deficiency (VLCAD): An evidence- and consensus-based approach.
S. V. van Calcar, M. Sowa, F. Rohr, J. Beazer +8 more
2020Molecular Genetics and Metabolism63 citations Open access
Semantic Scholar
Nutrition management guideline for propionic acidemia: An evidence- and consensus-based approach.
E. Jurecki, K. Ueda, D. Frazier, F. Rohr +10 more
2019Molecular Genetics and Metabolism62 citations Open access
Semantic Scholar
Barriers to successful dietary control among pregnant women with phenylketonuria
Amanda S. Brown, P. Fernhoff, S. Waisbren, D. Frazier +8 more
2002Genetics in Medicine60 citations Open access
Semantic Scholar
Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management.
K. North, Mark S. Korson, Yasodha R. Gopal, F. Rohr +3 more
1995Jornal de Pediatria60 citations
Semantic Scholar
A re-evaluation of life-long severe galactose restriction for the nutrition management of classic galactosemia.
S. V. van Calcar, L. Bernstein, F. Rohr, C. Scaman +2 more
2014Molecular Genetics and Metabolism53 citations
Semantic Scholar
New England Maternal PKU Project: prospective study of untreated and treated pregnancies and their outcomes.
F. Rohr, L. B. Doherty, S. Waisbren, I. Bailey +3 more
1987Jornal de Pediatria53 citations
Semantic Scholar
Metabolomic changes demonstrate reduced bioavailability of tyrosine and altered metabolism of tryptophan via the kynurenine pathway with ingestion of medical foods in phenylketonuria
D. Ney, S. Murali, Bridget M. Stroup, N. Nair +3 more
2017Molecular Genetics and Metabolism50 citations Open access
Semantic Scholar
Plasma amino acid levels after single-dose aspartame consumption in phenylketonuria, mild hyperphenylalaninemia, and heterozygous state for phenylketonuria.
Benjamin Caballero, B. E. Mahon, F. Rohr, H. Levy +1 more
1986Jornal de Pediatria41 citations
Semantic Scholar
Tyrosine supplementation in the treatment of maternal phenylketonuria.
F. Rohr, D. Lobbregt, Harvey L. Levy
1998American Journal of Clinical Nutrition36 citations Open access
Semantic Scholar
Skeletal health in adult patients with classic galactosemia
L. Batey, C. Welt, F. Rohr, A. Wessel +6 more
2013Osteoporosis International35 citations
Semantic Scholar
Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria.
Bridget M. Stroup, N. Nair, S. Murali, Katarzyna A. Broniowska +3 more
2018Journal of NutriLife33 citations Open access
Semantic Scholar
Detection of phenylketonuria in the very early newborn blood specimen.
L. B. Doherty, F. Rohr, Harvey L. Levy
1991Pediatrics32 citations
Semantic Scholar
The Resource Mothers Study of Maternal Phenylketonuria: Preliminary findings
F. Rohr, A. Munier, D. Sullivan, I. Bailey +11 more
2004Journal of Inherited Metabolic Disease30 citations
Semantic Scholar
Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal Characteristics.
S. Waisbren, F. Rohr, V. Anastasoaie, M. Brown +5 more
2015JIMD Reports29 citations Open access
Semantic Scholar
Nutrition Management of Inherited Metabolic Diseases
L. Bernstein, F. Rohr, J. R. Helm
201529 citations
Semantic Scholar
Intake and Blood Levels of Fatty Acids in Treated Patients With Phenylketonuria
P. Acosta, S. Yannicelli, Rani H. Singh, Louis J. Eisas +6 more
2001Journal of Pediatric Gastroenterology and Nutrition - JPGN29 citations Open access
Semantic Scholar
Nutrition management of PKU with pegvaliase therapy: update of the web-based PKU nutrition management guideline recommendations
A. Cunningham, F. Rohr, P. Splett, S. Mofidi +4 more
2023Orphanet Journal of Rare Diseases28 citations Open access
Semantic Scholar
Nutrition status of adults with phenylketonuria treated with pegvaliase.
K. Viau, A. Wessel, L. Martell, S. Sacharow +1 more
2021Molecular Genetics and Metabolism28 citations
Semantic Scholar
The New England Maternal PKU Project: identification of at-risk women.
S. Waisbren, L. B. Doherty, I. Bailey, F. Rohr +1 more
1988American Journal of Public Health28 citations Open access
Semantic Scholar
Metabolomic Insights into the Nutritional Status of Adults and Adolescents with Phenylketonuria Consuming a Low-Phenylalanine Diet in Combination with Amino Acid and Glycomacropeptide Medical Foods
Bridget M. Stroup, D. Ney, S. Murali, F. Rohr +3 more
2017Journal of Nutrition and Metabolism26 citations Open access
Semantic Scholar
Necessity of complete intake of phenylalanine-free amino acid mixture for metabolic control of phenylketonuria.
Gloria P. Duran, F. Rohr, Alfred E. Slonim, F. Güttler +1 more
1999Journal of the American Dietetic Association26 citations
Semantic Scholar
Bridging evidence and consensus methodology for inherited metabolic disorders: creating nutrition guidelines.
Rani H. Singh, F. Rohr, P. Splett
2013Journal of Evaluation In Clinical Practice24 citations
Semantic Scholar
Intake of major nutrients by women in the Maternal Phenylketonuria (MPKU) Study and effects on plasma phenylalanine concentrations.
P. Acosta, Kimberly Matalon, L. Castiglioni, F. Rohr +3 more
2001American Journal of Clinical Nutrition24 citations Open access
Semantic Scholar
Nutrition support for glutaric acidemia type I.
S. Yannicelli, F. Rohr, M. Warman
1994Journal of the American Dietetic Association23 citations
Semantic Scholar
Multiclinic Observations on the Simplified Diet in PKU
L. Bernstein, C. Burns, Melissa Sailer-Hammons, A. Kurtz +1 more
2017Journal of Nutrition and Metabolism21 citations Open access
Semantic Scholar
Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acids.
Louisa Kalsner, F. Rohr, K. Strauss, M. Korson +1 more
2001Jornal de Pediatria21 citations
Semantic Scholar
Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase
J. C. Rocha, H. Bausell, A. Bélanger-Quintana, L. Bernstein +6 more
2021Molecular Genetics and Metabolism Reports20 citations Open access
Semantic Scholar
Social factors and the meaning of food in adherence to medical diets: results of a maternal phenylketonuria summer camp
S. Waisbren, H. Rokni, I. Bailey, F. Rohr +2 more
1997Journal of Inherited Metabolic Disease20 citations
Semantic Scholar
Adherence to tetrahydrobiopterin therapy in patients with phenylketonuria.
F. Rohr, A. Wessel, Matthew Brown, K. Charette +1 more
2015Molecular Genetics and Metabolism19 citations
Semantic Scholar
Management of a Woman With Maple Syrup Urine Disease During Pregnancy, Delivery, and Lactation.
A. Wessel, K. Mogensen, F. Rohr, M. Erick +6 more
2015JPEN - Journal of Parenteral and Enteral Nutrition19 citations
Semantic Scholar
Galactose content of legumes, caseinates, and some hard cheeses: implications for diet treatment of classic galactosemia.
S. V. van Calcar, L. Bernstein, F. Rohr, S. Yannicelli +2 more
2014Journal of Agricultural and Food Chemistry19 citations
Semantic Scholar
Recommendations for Personalized Dietary Adjustments Based on Patient Response to Tetrahydrobiopterin (BH4) in Phenylketonuria
Rani H. Singh, E. Jurecki, F. Rohr
200819 citations
Semantic Scholar
Acceptability of a new modular protein substitute for the dietary treatment of phenylketonuria
F. Rohr, A. Munier, Harvey L. Levy
2001Journal of Inherited Metabolic Disease16 citations
Semantic Scholar
Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study.
Farrah Rajabi, F. Rohr, A. Wessel, L. Martell +4 more
2019Molecular Genetics and Metabolism15 citations
Semantic Scholar
Nutrition Management of Fatty Acid Oxidation Disorders
F. Rohr
201511 citations
Semantic Scholar
Use of the Guthrie bacterial inhibition assay to monitor blood phenylalanine for dietary treatment of phenylketonuria
F. Rohr, E. Allred, M. Turner, Jane R. Simmons +1 more
199611 citations
Semantic Scholar
Discontinuation of Pegvaliase therapy during maternal PKU pregnancy and postnatal breastfeeding: A case report
F. Rohr, A. Kritzer, C. Harding, K. Viau +1 more
2020Molecular Genetics and Metabolism Reports9 citations Open access
Semantic Scholar
Brain MRS glutamine as a biomarker to guide therapy of hyperammonemic coma.
A. O'Donnell-Luria, A. Lin, S. Merugumala, F. Rohr +13 more
2017Molecular Genetics and Metabolism9 citations Open access
Semantic Scholar
Nutrition and reproductive outcome in maternal phenylketonuria
K. Michals, P. Acosta, V. Austin, L. Castiglioni +3 more
2009European Journal of Pediatrics9 citations
Semantic Scholar

Frequent co-authors

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H. Levy×18
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H. Levy — researcher profile on SciRah
Rani H. Singh×11
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Rani H. Singh — researcher profile on SciRah
S. Waisbren×10
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A. Wessel×8
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A. Wessel — researcher profile on SciRah

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P. Splett — researcher profile on SciRah

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G. Berry — researcher profile on SciRah

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D. Frazier — researcher profile on SciRah

S. Yannicelli×6

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S. Yannicelli — researcher profile on SciRah

L. Bernstein×6

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L. Bernstein — researcher profile on SciRah

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P. Acosta — researcher profile on SciRah

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S. V. van Calcar — researcher profile on SciRah

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