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Monica Hsiung Wojcik, M.D.

Concepts (297)

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Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Intensive Care Units, Neonatal1320248333.420 Why?
Genetic Diseases, Inborn620246012.630 Why?
Rare Diseases820246192.360 Why?
Genetic Testing18202435312.120 Why?
Infant Mortality420217571.560 Why?
Infant, Newborn, Diseases220225921.060 Why?
Congenital Abnormalities220217041.040 Why?
Genomics8202457941.030 Why?
Infant, Newborn322024261811.010 Why?
Hydrops Fetalis120231090.840 Why?
Phenotype212024165460.840 Why?
Accidents120231660.830 Why?
Beckwith-Wiedemann Syndrome22022440.830 Why?
Clubfoot12023870.820 Why?
Jaundice, Neonatal12022710.800 Why?
Genetic Variation6202465510.800 Why?
Developmental Disabilities6202315040.790 Why?
Death, Sudden120233020.780 Why?
Abnormalities, Multiple4202214150.770 Why?
CHARGE Syndrome12021330.770 Why?
Vital Statistics12021310.770 Why?
Pierre Robin Syndrome120231170.750 Why?
Infant292024360600.740 Why?
Neonatology120221400.720 Why?
Bilirubin120224380.710 Why?
Amniocentesis120201150.690 Why?
Hypocalcemia120211990.680 Why?
DiGeorge Syndrome120211850.670 Why?
Intestinal Obstruction120234340.660 Why?
Olivopontocerebellar Atrophies12018190.640 Why?
Vestibular Diseases120212290.630 Why?
Growth Disorders120236530.630 Why?
Face2202110170.600 Why?
Hematologic Diseases120214960.580 Why?
Marfan Syndrome120192360.570 Why?
Stillbirth120203680.570 Why?
Spinal Muscular Atrophies of Childhood120181140.570 Why?
Neonatal Screening120215950.540 Why?
Ribonucleoproteins120193720.540 Why?
Sequence Analysis, DNA3202447130.510 Why?
Elastin120173010.510 Why?
Sudden Infant Death120182910.510 Why?
Critical Illness4202427090.500 Why?
Delayed Diagnosis220224640.490 Why?
Williams Syndrome120171930.490 Why?
Chromosome Aberrations2202017640.480 Why?
Mutation, Missense8202425660.470 Why?
Cause of Death2202337250.460 Why?
Anemia1202315110.450 Why?
Turner Syndrome120141300.440 Why?
Genetic Association Studies5202427170.430 Why?
Fetus1202018590.410 Why?
Humans7920247606210.400 Why?
Pulmonary Emphysema120176880.390 Why?
Jumonji Domain-Containing Histone Demethylases220241740.390 Why?
Genetic Predisposition to Disease62021177900.380 Why?
Mutation112024299320.360 Why?
Nervous System Malformations220232440.350 Why?
Optic Atrophy22020780.330 Why?
Histone Demethylases220233230.330 Why?
Neoplasm Proteins1202136100.330 Why?
Health Status Disparities1202018300.320 Why?
Healthcare Disparities2202233880.310 Why?
Craniofacial Abnormalities220223150.300 Why?
Autopsy2202310070.290 Why?
Health Services Accessibility3202353970.290 Why?
Chromosome Disorders220194990.270 Why?
Child252024798060.260 Why?
Amyloid120098420.240 Why?
RNA, Small Nuclear12024740.230 Why?
DNA-Binding Proteins1202195850.230 Why?
Syndrome5202432800.230 Why?
Chromosome Mapping2202246250.220 Why?
Anodontia12023500.210 Why?
Lesch-Nyhan Syndrome12022160.210 Why?
Prenatal Diagnosis2202012640.210 Why?
Female3420243912700.210 Why?
Vena Cava, Superior120231970.200 Why?
Male3120243597440.200 Why?
Polyadenylation120231170.200 Why?
Nuclear Proteins4202457910.200 Why?
Mixed Function Oxygenases120232650.200 Why?
Wolf-Hirschhorn Syndrome1202150.190 Why?
Histones3202025830.190 Why?
Infant, Premature2202220920.190 Why?
Pregnancy62023297490.180 Why?
Muscle Hypotonia120221600.180 Why?
Neurodegenerative Diseases2202010840.180 Why?
Flavoproteins12020400.180 Why?
Insulin Resistance1201439590.180 Why?
Anorexia Nervosa1200913610.180 Why?
Seizures4202129170.180 Why?
Infant, Low Birth Weight220228590.170 Why?
Genome, Human3202444170.170 Why?
Blood Glucose1201463810.170 Why?
Nervous System Diseases2202116470.170 Why?
Insulin1201465970.170 Why?
Hernia, Abdominal12020560.170 Why?
Vomiting120236500.170 Why?
Haploinsufficiency220223290.170 Why?
POU Domain Factors12019470.170 Why?
Chromosome Inversion120201200.170 Why?
Aneuploidy220205510.170 Why?
Heart Septal Defects, Ventricular120224910.170 Why?
Protein Conformation4202039690.160 Why?
Retrospective Studies102024803720.160 Why?
Acetyltransferases120202310.160 Why?
Transcription Factor AP-212019790.160 Why?
Chromosomes, Human, Pair 4120203770.160 Why?
Phenylketonurias120201230.160 Why?
DNA-Directed RNA Polymerases120213670.160 Why?
Diabetes Insipidus120191440.160 Why?
N-Acetylglucosaminyltransferases120191670.160 Why?
Phosphoric Monoester Hydrolases120204120.150 Why?
Transcription Factors42023121030.150 Why?
Nuclear Receptor Subfamily 1, Group F, Member 112018480.150 Why?
Fatal Outcome2202018320.150 Why?
Canada1202321280.150 Why?
Cleft Lip120235040.140 Why?
DNA Copy Number Variations2202420130.140 Why?
Genomic Imprinting120193300.140 Why?
Ductus Arteriosus, Patent120192180.140 Why?
Catalytic Domain120197060.140 Why?
Dystonia120203640.140 Why?
Cleft Palate120235870.140 Why?
Body Height1202315700.140 Why?
Histone-Lysine N-Methyltransferase120216780.140 Why?
Alleles4202468980.140 Why?
Cerebellar Ataxia120181490.140 Why?
Adolescent112024878100.140 Why?
Bone Density1200935340.140 Why?
Chromosomes, Human, Pair 7120173100.140 Why?
Child, Preschool112024420630.130 Why?
Chylothorax12017830.130 Why?
Noonan Syndrome120171200.130 Why?
Zebrafish3202329970.130 Why?
Fingers120195060.130 Why?
DNA Helicases120218540.130 Why?
Spasms, Infantile120192960.130 Why?
Family Characteristics1202010010.130 Why?
Genes, Dominant120188630.120 Why?
Genotype52024129600.120 Why?
GTPase-Activating Proteins120184750.120 Why?
Homozygote1202017880.120 Why?
Gene Dosage1201912180.120 Why?
Young Adult82024587410.120 Why?
Brain Edema120196030.120 Why?
Mitochondrial Proteins120209790.120 Why?
Models, Molecular3201954340.120 Why?
RNA-Binding Proteins1202318940.120 Why?
United States52023724610.120 Why?
Infant, Premature, Diseases120207080.120 Why?
Cytoplasm1201915160.120 Why?
Epilepsy2202032670.110 Why?
Point-of-Care Systems1202212040.110 Why?
Spliceosomes220241290.110 Why?
Transcriptional Activation1201917550.110 Why?
Information Storage and Retrieval120188220.110 Why?
Cytoskeletal Proteins1201813430.100 Why?
Chromosome Deletion1201713870.100 Why?
Exons3202323880.100 Why?
Obesity12014129220.100 Why?
Forecasting1202129320.100 Why?
Hospitals, Pediatric1202118540.100 Why?
Cohort Studies32024413350.100 Why?
Cell Adhesion1201830940.100 Why?
Gene Deletion1201926680.100 Why?
Glucose Tolerance Test1201411750.100 Why?
In Situ Hybridization, Fluorescence1201725060.090 Why?
Adult1020242199940.090 Why?
Carrier Proteins2202349380.090 Why?
Heterozygote3202427980.090 Why?
High-Throughput Nucleotide Sequencing1202236160.090 Why?
Amino Acid Sequence22019134510.090 Why?
Islet Amyloid Polypeptide12009420.090 Why?
Intracellular Signaling Peptides and Proteins1202028730.090 Why?
Polymerase Chain Reaction1201960680.090 Why?
Human Growth Hormone120146380.080 Why?
Referral and Consultation1202235980.080 Why?
Hospitals1202239280.080 Why?
Introns220239780.080 Why?
Pedigree3202145780.080 Why?
Fibroblast Growth Factors120148690.080 Why?
Brain Diseases1201715400.080 Why?
Autistic Disorder1201812160.080 Why?
Adaptor Proteins, Signal Transducing1201928950.080 Why?
Methylation2202110820.080 Why?
Mitochondria1202136000.070 Why?
Risk Factors32021743590.070 Why?
Gene Expression Regulation32020119030.070 Why?
Heart Defects, Congenital1202446730.070 Why?
Palliative Care1202236070.070 Why?
Transcription, Genetic1202175930.070 Why?
Computational Biology1201935050.070 Why?
Patient Selection1201842830.070 Why?
Quality Improvement1202138360.070 Why?
Neuropsychological Tests1201970210.070 Why?
Gene Expression1201875880.060 Why?
Minority Groups2202412010.060 Why?
Prevalence22019156870.060 Why?
Delivery of Health Care1202353250.060 Why?
Predictive Value of Tests12020152890.060 Why?
Protein Processing, Post-Translational2202319740.060 Why?
Animals920231679630.060 Why?
Lipids1201433360.050 Why?
RNA Splice Sites120242110.050 Why?
Mice52023812080.050 Why?
Hypoxanthine Phosphoribosyltransferase12022690.050 Why?
Disease Models, Animal22018181370.050 Why?
Magnetic Resonance Imaging52020362900.050 Why?
Loss of Heterozygosity120236590.050 Why?
Minority Health12022810.050 Why?
Brain42024269510.050 Why?
3' Untranslated Regions120235140.050 Why?
RNA Transport12020450.040 Why?
Acyl-CoA Oxidase1202080.040 Why?
Middle Aged520232203520.040 Why?
Follow-Up Studies12022392610.040 Why?
Chromosome Breakpoints12020930.040 Why?
Silver-Russell Syndrome1201950.040 Why?
Estonia12019540.040 Why?
Cyclin-Dependent Kinase Inhibitor p5712019430.040 Why?
Embryo, Nonmammalian120239000.040 Why?
Sequence Homology120191950.040 Why?
Hernia, Diaphragmatic120202460.040 Why?
Cell Nucleolus120191560.040 Why?
Exodeoxyribonucleases120201950.040 Why?
Risk Assessment12020241230.040 Why?
Oxidative Phosphorylation120214950.040 Why?
Prader-Willi Syndrome12019760.040 Why?
Focus Groups1202413780.040 Why?
Logistic Models22024133140.040 Why?
Chromosomes, Human, Pair 10120192760.040 Why?
Ataxia120203050.040 Why?
Facies120192230.040 Why?
Adenosine Triphosphatases120228320.040 Why?
Finland120196030.040 Why?
Chromatin2201929380.040 Why?
Protein Subunits120219430.040 Why?
Genetic Complementation Test120185550.040 Why?
Early Diagnosis1202211800.040 Why?
Angelman Syndrome120191400.040 Why?
Chromosomes, Human, Pair 1120196350.030 Why?
Multicenter Studies as Topic1202217220.030 Why?
Glycosylation1201910960.030 Why?
Hernia, Ventral120202140.030 Why?
Purkinje Cells120182260.030 Why?
Larva120185090.030 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 11120172240.030 Why?
Antigens, Surface1202016080.030 Why?
DNA, Mitochondrial120218580.030 Why?
RNA, Messenger22021127660.030 Why?
Access to Information120183200.030 Why?
DNA Methylation2201943730.030 Why?
Edema120197690.030 Why?
Structure-Activity Relationship1202030840.030 Why?
Zebrafish Proteins1202010060.030 Why?
Peripheral Nervous System Diseases120207080.030 Why?
Neoplasms12023220720.030 Why?
Repressor Proteins1202429810.030 Why?
Ubiquitin-Protein Ligases1202318890.030 Why?
Forkhead Transcription Factors1202016120.030 Why?
Age of Onset1202033010.030 Why?
Gene Expression Regulation, Developmental1202436040.030 Why?
Glycoproteins1202022080.030 Why?
Germ-Line Mutation1202018410.030 Why?
Polymorphism, Genetic1202342910.030 Why?
Consensus1202231130.030 Why?
Databases, Genetic1201917380.030 Why?
Ultrasonography, Prenatal1202017450.020 Why?
Body Mass Index12009129140.020 Why?
Diet1200980100.020 Why?
Cell Nucleus1202029070.020 Why?
Phosphoproteins1202024400.020 Why?
Genetic Markers1201726080.020 Why?
Fibroblasts1202140900.020 Why?
Health Personnel1202433100.020 Why?
Drosophila melanogaster1201917100.020 Why?
Information Dissemination1201811310.020 Why?
Drosophila Proteins1201916990.020 Why?
Patient Discharge1202234760.020 Why?
Cross-Sectional Studies12009259420.020 Why?
Hippocampus1202037380.020 Why?
Echocardiography1202049810.020 Why?
Chronic Disease1202292870.020 Why?
Epigenesis, Genetic1202037580.020 Why?
Cell Line12019156200.020 Why?
Recurrence1201784820.020 Why?
Prospective Studies22019543030.020 Why?
Severity of Illness Index12022158400.010 Why?
Software1201844190.010 Why?
Aged, 80 and over22019589950.010 Why?
Gene Expression Profiling1201994110.010 Why?
Diagnosis, Differential12018129650.010 Why?
Genome-Wide Association Study12017126260.010 Why?
Signal Transduction12020233760.010 Why?
Aged220191691520.010 Why?
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© 2024 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.