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bitter taste (2) 2
body mass index (2) 2
case-control studies (2) 2
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genetics (2) 2
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sensitivity (2) 2
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taste (2) 2
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acanthosis nigricans - etiology (1) 1
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1. Full Text MC4R-dependent suppression of appetite by bone-derived lipocalin 2
by Mosialou, Ioanna and Shikhel, Steven and Liu, Jian-Min and Maurizi, Antonio and Luo, Na and He, Zhenyan and Huang, Yiru and Zong, Haihong and Friedman, Richard A and Barasch, Jonathan and Lanzano, Patricia and Deng, Liyong and Leibel, Rudolph L and Rubin, Mishaela and Nicholas, Thomas and Chung, Wendy and Zeltser, Lori M and Williams, Kevin W and Pessin, Jeffrey E and Kousteni, Stavroula
Nature, ISSN 0028-0836, 03/2017, Volume 543, Issue 7645, pp. 385 - 390
Bone has recently emerged as a pleiotropic endocrine organ that secretes at least two hormones, FGF23 and osteocalcin, which regulate kidney function and... 
BODY-WEIGHT | GREEN FLUORESCENT PROTEIN | INSULIN-RECEPTOR | GLUCOSE-HOMEOSTASIS | OBESITY | MELANOCORTIN RECEPTORS | FOOD-INTAKE | MULTIDISCIPLINARY SCIENCES | NEURONS | ENERGY-METABOLISM | ADIPOSE-TISSUE | Insulin Resistance | Homeostasis | Male | Receptor, Melanocortin, Type 4 - metabolism | Thinness - metabolism | Blood-Brain Barrier - metabolism | Eating - physiology | Obesity - metabolism | Paraventricular Hypothalamic Nucleus - cytology | Insulin - metabolism | Animals | Hypothalamus - metabolism | Lipocalin-2 - metabolism | Hypothalamus - cytology | Bone and Bones - metabolism | Glucose - metabolism | Female | Mice | Neurons - metabolism | Appetite Regulation - physiology | Osteoblasts - metabolism | Cyclic AMP - metabolism | Insulin Secretion | Bone and Bones - cytology | Appetite | Prevention | Usage | Physiological aspects | Bones | Hormones | Health aspects | Proteins | Obesity | Blood-brain barrier | Rodents | Expenditures | Glucose | Mutation | Metabolism | Insulin | Food
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2. Full Text Common variants in the CD36 gene are associated with oral fat perception, fat preferences, and obesity in African Americans
by Keller, Kathleen L and Liang, Lisa C.H and Sakimura, Johannah and May, Daniel and Van Belle, Christopher and Breen, Cameron and Driggin, Elissa and Tepper, Beverly J and Lanzano, Patricia C and Deng, Liyong and Chung, Wendy K
Obesity, ISSN 1930-7381, 05/2012, Volume 20, Issue 5, pp. 1066 - 1073
Animal studies show that CD36, a fatty acid translocase, is involved in fat detection and preference, but these findings have not been reported in humans. The... 
METABOLIC SYNDROME | NUTRITION & DIETETICS | DIETARY-FAT | WAIST CIRCUMFERENCE | DAIRY-PRODUCTS | ENDOCRINOLOGY & METABOLISM | SENSITIVITY | RATS | TASTE | RISK | FOODS | ACID TRANSPORT | CD36 Antigens - genetics | Food Preferences - psychology | Obesity - psychology | Humans | Middle Aged | Male | Obesity - genetics | Food Preferences - ethnology | Young Adult | Dietary Fats | Discrimination (Psychology) | Adult | Female | Surveys and Questionnaires | Choice Behavior | Cross-Sectional Studies | African Americans - genetics | Genotype | African Americans - statistics & numerical data | Saliva - metabolism | Adolescent | Perception | Aged | Polymorphism, Single Nucleotide | Taste | African Americans - psychology | African Americans | Obesity | Genetics | Oils & fats | Food products | Preferences
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3. Full Text Whole‐Exome sequencing identifies novel LEPR mutations in individuals with severe early onset obesity
by Gill, Richard and Cheung, Yee Him and Shen, Yufeng and Lanzano, Patricia and Mirza, Nazrat M and Ten, Svetlana and Maclaren, Noel K and Motaghedi, Roja and Han, Joan C and Yanovski, Jack A and Leibel, Rudolph L and Chung, Wendy K
Obesity, ISSN 1930-7381, 02/2014, Volume 22, Issue 2, pp. 576 - 584
Objective: Obesity is a major public health problem that increases the risk for a broad spectrum of comorbid conditions. Despite evidence for a strong genetic... 
CONGENITAL LEPTIN DEFICIENCY | NUTRITION & DIETETICS | ENDOCRINOLOGY & METABOLISM | FRAMEWORK | BODY-MASS INDEX | RECEPTOR | GENERATION | Body Mass Index | Pediatric Obesity - physiopathology | Frameshift Mutation | Receptors, Leptin - genetics | Humans | Pediatric Obesity - blood | Family Health | Infant | Male | Pediatric Obesity - genetics | Insulin - blood | Pediatric Obesity - metabolism | Sequence Analysis, DNA | Exome | Receptors, Leptin - chemistry | Acanthosis Nigricans - etiology | Homozygote | Leptin - blood | Pedigree | Adolescent | Female | Consanguinity | Receptors, Leptin - metabolism | Child | Obesity | Pathogenesis | Mortality | Families & family life | Genomes | Studies | Body mass index | Medical laboratories | DNA methylation | Mutation | Genetic testing | Age | Deoxyribonucleic acid--DNA | genetics of obesity | leptin receptor
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4. Full Text Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice
by Stratigopoulos, George and Martin Carli, Jayne F and O’Day, Diana R and Wang, Liheng and LeDuc, Charles A and Lanzano, Patricia and Chung, Wendy K and Rosenbaum, Michael and Egli, Dieter and Doherty, Daniel A and Leibel, Rudolph L
Cell Metabolism, ISSN 1550-4131, 05/2014, Volume 19, Issue 5, pp. 767 - 779
Common polymorphisms in the first intron of are associated with increased body weight in adults. Previous studies have suggested that a CUX1-regulatory element... 
TRANSPORT | ENERGY-EXPENDITURE | SYNDROME JOUBERT-SYNDROME | TRANSITION ZONE | FOOD-INTAKE | ENDOCRINOLOGY & METABOLISM | BARDET-BIEDL-SYNDROME | LEPTIN RECEPTOR | ADULT OBESITY | GENOME-WIDE ASSOCIATION | BASAL BODY PROTEIN | CELL BIOLOGY | Receptors, Leptin - genetics | Introns | Humans | Mice, Inbred C57BL | Cells, Cultured | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | Leptin - genetics | Hypothalamus | Adiposity - genetics | Eating - genetics | Cilia - genetics | Proteins - genetics | Animals | Adaptor Proteins, Signal Transducing - genetics | Weight Gain - genetics | Female | Polymorphism, Genetic - genetics | Mice | STAT3 Transcription Factor - genetics | Fibroblasts - metabolism | Molecular genetics | Leptin | Genes
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5. Full Text Sex Differences in the Effects of Inherited Bitter Thiourea Sensitivity on Body Weight in 4-6-Year-Old Children
by Keller, Kathleen L and Reid, Adrienne and MacDougall, Megan C and Cassano, Hope and Song, Joo Lee and Deng, Liyong and Lanzano, Patricia and Chung, Wendy K and Kissileff, Harry R
Obesity, ISSN 1930-7381, 06/2010, Volume 18, Issue 6, pp. 1194 - 1200
Previous studies have shown that inherited taste blindness to bitter compounds like 6‐ n ‐propylthiouracil (PROP) may be a risk factor for obesity, but this... 
FOOD PREFERENCE | GENETIC SENSITIVITY | FAT PERCEPTION | NUTRITION & DIETETICS | ENDOCRINOLOGY & METABOLISM | PATTERNS | PROP TASTER STATUS | ENERGY-INTAKE | 6-N-PROPYLTHIOURACIL PROP | MIDDLE-AGED WOMEN | TAS2R38 | ENVIRONMENTAL-INFLUENCES | Taste Disorders - genetics | Humans | Genetic Diseases, Inborn - genetics | Child, Preschool | Male | Risk | Propylthiouracil | Genetic Diseases, Inborn - epidemiology | Body Weight - genetics | Obesity - genetics | Genetic Variation - physiology | Genetic Diseases, Inborn - complications | Female | Thiourea | Taste - genetics | Child | Body Mass Index | Genetic Predisposition to Disease | Obesity - complications | Genotype | Taste Disorders - epidemiology | Sex Characteristics | Obesity - epidemiology | Receptors, G-Protein-Coupled - genetics | Taste Disorders - complications | Body Weight - physiology
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6. Full Text Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies
by Ma, Lijiang and Tierney, Elif Seda Selamet and Lee, Teresa and Lanzano, Patricia and Chung, Wendy K
Cardiology in the Young, ISSN 1047-9511, 04/2012, Volume 22, Issue 2, pp. 194 - 201
Background: Heterotaxy syndrome is caused by left-right asymmetry disturbances and is associated with abnormal lateralisation of the abdominal and thoracic... 
LEFTYA | Left-right asymmetry | CFC1 | congenital cardiac defect | SITUS-INVERSUS | CARDIAC & CARDIOVASCULAR SYSTEMS | GREAT-ARTERIES | LATERALITY DEFECTS | ZINC-FINGER DOMAIN | MALFORMATIONS | GENE | CONGENITAL HEART-DISEASE | LEFT-RIGHT AXIS | FUNCTIONAL-ANALYSIS | PEDIATRICS | Fetus - abnormalities | Heterotaxy Syndrome - genetics | Cardiovascular Abnormalities - complications | Humans | Intercellular Signaling Peptides and Proteins - genetics | Cardiovascular Abnormalities - genetics | Genotype | Male | Transcription Factors - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Pregnancy | Left-Right Determination Factors - genetics | Activin Receptors, Type II - genetics | Heterotaxy Syndrome - complications | Female | New York City - epidemiology | Mutation | Sequence Analysis | Cardiovascular Abnormalities - epidemiology | left-right asymmetry | congenital heart defect
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7. Full Text Bitter taste phenotype and body weight predict children's selection of sweet and savory foods at a palatable test-meal
by Keller, Kathleen L and Olsen, Annemarie and Cravener, Terri L and Bloom, Rachel and Chung, Wendy K and Deng, Liyong and Lanzano, Patricia and Meyermann, Karol
Appetite, ISSN 0195-6663, 06/2014, Volume 77, pp. 115 - 123
Previous studies show that children who are sensitive to the bitter taste of 6-n-propylthiouracil (PROP) report more frequent intake of sweets and less... 
Obesity | Children | PROP phenotype | Eating behavior | Bitter taste | IRISH CHILDREN | MASS INDEX | SENSORY PERCEPTION | PROP | SENSITIVITY | FAT PERCEPTION | NUTRITION & DIETETICS | PREFERENCES | ADOLESCENTS | BEHAVIORAL SCIENCES | 6-N-PROPYLTHIOURACIL | RECEPTOR GENE TAS2R38 | Food Preferences | Body Weight | Humans | Child, Preschool | Genotype | Male | Propylthiouracil | Phenotype | Diet | Dietary Fats | Taste Buds | Female | Taste Perception - genetics | Dietary Sucrose | Taste - genetics | Meals | Child | Receptors, Cell Surface - genetics | Body weight | Taste | Natural selection
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8. Full Text Corrigendum: MC4R-dependent suppression of appetite by bone-derived lipocalin 2
by Mosialou, Ioanna and Shikhel, Steven and Liu, Jian-Min and Maurizi, Antonio and Luo, Na and He, Zhenyan and Huang, Yiru and Zong, Haihong and Friedman, Richard A and Barasch, Jonathan and Lanzano, Patricia and Deng, Liyong and Leibel, Rudolph L and Rubin, Mishaela and Nickolas, Thomas and Chung, Wendy and Zeltser, Lori M and Williams, Kevin W and Pessin, Jeffrey E and Kousteni, Stavroula
Nature, ISSN 0028-0836, 06/2017, Volume 546, Issue 7658, p. 440
This corrects the article DOI: 10.1038/nature21697. 
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9. Full Text Erratum: Corrigendum: MC4R-dependent suppression of appetite by bone-derived lipocalin 2
by Mosialou, Ioanna and Shikhel, Steven and Liu, Jian-Min and Maurizi, Antonio and Luo, Na and He, Zhenyan and Huang, Yiru and Zong, Haihong and Friedman, Richard A and Barasch, Jonathan and Lanzano, Patricia and Deng, Liyong and Leibel, Rudolph L and Rubin, Mishaela and Nickolas, Thomas and Chung, Wendy and Zeltser, Lori M and Williams, Kevin W and Pessin, Jeffrey E and Kousteni, Stavroula
Nature, ISSN 0028-0836, 06/2017, Volume 546, Issue 7658, pp. 440 - 440
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10. Full Text Bitter taste phenotype and body weight predict children’s selection of sweet and savory foods at a palatable test-meal
by Keller, Kathleen L and Olsen, Annemarie and Cravener, Terri L and Bloom, Rachel and Chung, Wendy K and Deng, Liyong and Lanzano, Patricia and Meyermann, Karol
Appetite, ISSN 0195-6663, 6/2014, Volume 77, pp. 113 - 121
Previous studies show that children who are sensitive to the bitter taste of 6-n-propylthiouracil (PROP) report more frequent intake of sweets and less... 
Obesity | Children | PROP phenotype | Eating behavior | Bitter taste
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11. Full Text Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations
by Lennon, Christen J and Birkeland, Andrew C and Nuñez, José Arturo Pacheco and Su, Gloria H and Lanzano, Patricia and Guzman, Edwin and Celis, Katrina and Eisig, Sidney B and Hoffman, David and Rendon, Maria Teresa Guerra and Ostos, Henry and Chung, Wendy K and Haddad, Joseph
The Laryngoscope, ISSN 0023-852X, 09/2012, Volume 122, Issue 9, pp. 2082 - 2087
Objectives/Hypothesis: Orofacial clefts are the most common craniofacial birth defects in humans, with the majority of orofacial clefts occurring as... 
Colombia | Cleft lip | candidate gene | MAFB | nonsyndromic | FOXE1 | Level of Evidence | ABCA4 | NOG | cleft palate | Honduras | 3b | MEDICINE, RESEARCH & EXPERIMENTAL | DISEQUILIBRIUM | VARIANTS | PALATE | LIP | OTORHINOLARYNGOLOGY | DISEASE | IRF6 | LINKAGE | Level of Evidence: 3b | REVEALS | United States - epidemiology | Confidence Intervals | Humans | Cleft Palate - surgery | Male | Cleft Palate - genetics | Case-Control Studies | Incidence | ATP-Binding Cassette Transporters - genetics | Female | Genetic Predisposition to Disease - epidemiology | Odds Ratio | Cleft Lip - surgery | Genome-Wide Association Study | Hispanic Americans - genetics | Genetic Association Studies | MafB Transcription Factor - genetics | Interferon Regulatory Factors - genetics | Genotype | Forkhead Transcription Factors - genetics | Cleft Lip - ethnology | Cleft Palate - ethnology | Cleft Lip - genetics | Pedigree | Honduras - ethnology | Alleles | Colombia - ethnology | Polymorphism, Single Nucleotide | Anopheles | Analysis | Medical societies | Genes | Genomics | DNA | Genetic research | Birth defects | Universities and colleges
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12. Full Text Whole-Exome sequencing identifies novelLEPRmutations in individuals with severe early onset obesity
: Exome Sequencing Identifies LEPR Mutations
by Gill, Richard and Cheung, Yee Him and Shen, Yufeng and Lanzano, Patricia and Mirza, Nazrat M and Ten, Svetlana and Maclaren, Noel K and Motaghedi, Roja and Han, Joan C and Yanovski, Jack A and Leibel, Rudolph L and Chung, Wendy K
Obesity, ISSN 1930-7381, 02/2014, Volume 22, Issue 2, pp. 576 - 584
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13. Full Text Glucokinase mutations in young children with hyperglycemia
by Codner, Ethel and Deng, Liyong and Pérez‐Bravo, Francisco and Román, Rossana and Lanzano, Patricia and Cassorla, Fernando and Chung, Wendy K
Diabetes/Metabolism Research and Reviews, ISSN 1520-7552, 09/2006, Volume 22, Issue 5, pp. 348 - 355
Background The etiology of mild hyperglycemia without ketoacidosis in young children is often unknown. Maturity onset diabetes of youth (MODY) is a form of... 
incidental hyperglycemia | MODY | diabetes | glucokinase | Diabetes | Glucokinase | Incidental hyperglycemia | GLUCOSE | DISEASE | ENDOCRINOLOGY & METABOLISM | HYPOGLYCEMIA | BETA-CELL GENES | HIGH PREVALENCE | FOR-GESTATIONAL-AGE | PATHOPHYSIOLOGY | Hepatocyte Nuclear Factor 1-alpha - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Glucokinase - genetics | Male | Hepatocyte Nuclear Factor 4 - genetics | DNA Primers | Hyperglycemia - genetics | Birth Weight | Pedigree | Base Sequence | Hyperglycemia - enzymology | Female | Mutation | Blood Glucose - metabolism | Child
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14. Full Text A De Novo Mutation (Gln2Stop) at the 5′ End of the SRY Gene Leads to Sex Reversal with Partial Ovarian Function
by Brown, Stephen and Yu, C.C and Lanzano, Patricia and Heller, Debra and Thomas, L and Warburton, Dorothy and Kitajewski, Jan and Stadtmauer, Laurel
The American Journal of Human Genetics, ISSN 0002-9297, 01/1998, Volume 62, Issue 1, pp. 189 - 192
Sex reversal | Ovarian function SRY gene | HMG BOX | XY FEMALES | GENETICS & HEREDITY | TESTIS-DETERMINING GENE | GONADAL-DYSGENESIS | MISSENSE MUTATIONS | NONSENSE MUTATION | REGION | Point Mutation | Codon | Sex Determination Processes | Sex-Determining Region Y Protein | Gonadal Dysgenesis - genetics | Humans | Karyotyping | Adult | Female | Transcription Factors | DNA-Binding Proteins - genetics | Nuclear Proteins | Letter
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15. Full Text Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser‐induced capillary fluorescence detection
by Day, Nancy S and Tadin, Marija and Christiano, Angela M and Lanzano, Patricia and Piomelli, Sergio and Brown, Stephen
Prenatal Diagnosis, ISSN 0197-3851, 08/2002, Volume 22, Issue 8, pp. 686 - 691
Prenatal diagnosis of sickle cell diseases has been available for several years, and our laboratory has performed over 1000 prenatal diagnoses. However,... 
prenatal diagnosis | fluorescent capillary electrophoresis | sickle cell | oligonucleotide ligation | Oligonucleotide ligation | Prenatal diagnosis | Fluorescent capillary electrophoresis | Sickle cell | ALLELE | DNA DIAGNOSTICS | OBSTETRICS & GYNECOLOGY | ELECTROPHORESIS | MUTATION | GENETICS & HEREDITY | EXPERIENCE | ANEMIA | LIGASE | Deoxyuracil Nucleotides | Hemoglobin A - genetics | Humans | Molecular Sequence Data | Templates, Genetic | Genotype | Hemoglobin, Sickle - genetics | DNA Ligases - metabolism | Pregnancy | Point Mutation | DNA - chemistry | Globins - genetics | Oligonucleotides - metabolism | Base Sequence | Sensitivity and Specificity | Hemoglobin C - genetics | Polymerase Chain Reaction | Female | Anemia, Sickle Cell - blood | Anemia, Sickle Cell - diagnosis | Electrophoresis, Capillary - methods | Prenatal Diagnosis - methods | Anemia, Sickle Cell - genetics
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16. Full Text Prenatal diagnosis of factor X deficiency using a combination of direct mutation detection and linkage analysis with an intragenic single nucleotide polymorphism
by Camire, Rodney and Ann Denchy, Ruth and Day, George A and Lanzano, Patricia and Sheth, Sujit and Brown, Stephen
Prenatal Diagnosis, ISSN 0197-3851, 06/2003, Volume 23, Issue 6, pp. 457 - 460
Objective To present a family in which it was possible to perform prenatal diagnosis for recessively inherited factor X deficiency using both direct mutation... 
CVS | linkage | SNP | factor X | coagulation | Factor X | Linkage | Coagulation | GENETICS & HEREDITY | OBSTETRICS & GYNECOLOGY | Factor X Deficiency - genetics | Humans | Male | DNA Mutational Analysis - methods | Factor X Deficiency - diagnosis | Pregnancy Trimester, First | DNA - blood | Pregnancy | Pedigree | Chorionic Villi Sampling | Polymorphism, Single Nucleotide - genetics | Adult | Female | Heterozygote | Mutation | Fetal Blood | Genetic Linkage
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