H. Hoyme

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A Framework for 3D Analysis of Facial Morphology in Fetal Alcohol Syndrome

Shiaofen Fang, Li Shen, Jing Wan, 2010, MIAR.

A Practical Clinical Approach to Diagnosis of Fetal Alcohol Spectrum Disorders: Clarification of the 1996 Institute of Medicine Criteria

H. Hoyme, P. May, W. Kalberg, 2005, Pediatrics.

Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis.

S. Fang, J. McLaughlin, I. Autti-Rämö, 2008, Orthodontics & craniofacial research.

Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations.

I. Autti-Rämö, Å. Fagerlund, H. Hoyme, 2007, Alcoholism, clinical and experimental research.

A Practical Clinical Approach to Diagnosis of Fetal Alcohol Spectrum Disorders: Clarification of the 1996 Institute of Medicine Criteria: In Reply

H. Eugene Hoyme, H. Hoyme, 2005, Pediatrics.

Prevalence and epidemiologic characteristics of FASD from various research methods with an emphasis on recent in-school studies.

David Buckley, Lisa H. Lu, Suzanne M. Houston, 2009, Developmental disabilities research reviews.

Prevalence of Fetal Alcohol Spectrum Disorders in 4 US Communities

J. A. Arroyo, C. Coles, R. Xu, 2018, JAMA.

Impaired delay and trace eyeblink conditioning in school-age children with fetal alcohol syndrome.

Ernesta M Meintjes, Christopher D Molteno, M. Stanton, 2011, Alcoholism, clinical and experimental research.

Facial Dysmorphism Across the Fetal Alcohol Spectrum

Peter Hammond, Ernesta M Meintjes, Christopher D Molteno, 2013, Pediatrics.

Genetic Disorders and the Fetus: Diagnosis, Prevention, and Treatment

H. Hoyme, 1987 .

Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review.

H. Hoyme, K. Jones, L. Seaver, 1998, American journal of medical genetics.

FETAL ANTICONVULSANT SYNDROME

H. Hoyme, O. Abdul-Rahman, E. Conover, 2021 .

Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation

C. Romano, E. Zackai, A. Battaglia, 2008, Pediatrics.

Additional EFNB1 mutations in craniofrontonasal syndrome

E. Zackai, I. Kaitila, J. Mulliken, 2008, American journal of medical genetics. Part A.

Vascular pathogenesis of limb defects. I. Radial artery anatomy in radial aplasia.

H. Hoyme, K. Jones, M. V. Van Allen, 1982, The Journal of pediatrics.

Minor anomalies: Diagnostic clues to aberrant human morphogenesis

H. Hoyme, H. Hoyme, 1993, Genetica.

Advances in whole-genome genetic testing: from chromosomes to microarrays.

H. Hoyme, P. Crotwell, Microarrays L. Crotwell, 2012, Current problems in pediatric and adolescent health care.

Ectopia lentis as the presenting and primary feature in Marfan syndrome

H. Hoyme, L. Hudgins, J. Bernstein, 2011, American journal of medical genetics. Part A.

Molecular genetic testing in pediatric practice: A subject review. Committee on Genetics.

H. Hoyme, C. Moore, J. Moeschler, 2016, Pediatrics.

22q13.3 deletion syndrome: A recognizable malformation syndrome associated with marked speech and language delay

H. Hoyme, M. Manning, K. Cusmano-Ozog, 2007, American journal of medical genetics. Part C, Seminars in medical genetics.

Vascular‐type disruptive defects in fetuses with homozygous α‐thalassemia: report of two cases and review of the literature

H. Vogel, H. Hoyme, Y. El‐Sayed, 2005, Prenatal diagnosis.

Phenotypic and genotypic heterogeneity in familial Milroy lymphedema.

H. Hoyme, R. Erickson, M. Witte, 1998, Lymphology.

Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature

J. Opitz, H. Hoyme, J. Fryns, 1987, American journal of medical genetics.

Athabascan brainstem dysgenesis syndrome

H. Hoyme, R. Erickson, C. Cunniff, 2003, American journal of medical genetics. Part A.

Early neonatal diagnosis of long-chain 3-hydroxyacyl coenzyme a dehydrogenase and mitochondrial trifunctional protein deficiencies.

N. Lehman, H. Hoyme, S. Hintz, 2002, Molecular genetics and metabolism.

Nablus mask‐like facial syndrome is caused by a microdeletion of 8q detected by array‐based comparative genomic hybridization

H. Hoyme, A. Cherry, S. Aradhya, 2006, American journal of medical genetics. Part A.

Identification of a balanced translocation carrier by spouse's low maternal serum alpha fetoprotein associated with an aneuploid fetus.

H. Hoyme, K. Byrne-Essif, 1990, Journal of medical genetics.

Congenital anomaly rate in offspring of mothers with diabetes treated with insulin lispro during pregnancy

H. Hoyme, E. Seely, R. Kaaja, 2005, Diabetic medicine : a journal of the British Diabetic Association.

FETAL ANTICONVULSANT SYNDROME

H. Hoyme, K. Kingham, R. Gallagher, 2005, Cassidy and Allanson's Management of Genetic Syndromes.

Maternal nutritional status as a contributing factor for the risk of fetal alcohol spectrum disorders.

H. Hoyme, P. May, J. Gossage, 2016, Reproductive toxicology.

Impact of Climate Changes on Wind Behaviour and Water Levels at the German North Sea Coast

H. Hoyme, W. Zielke, 2001 .

Patient and Physician Perceptions of Genetic Testing in Primary Care.

H. Hoyme, Eric A. Larson, S. Puumala, 2016, South Dakota medicine : the journal of the South Dakota State Medical Association.

Malignancy in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

E. Zackai, K. Sullivan, H. Hoyme, 2006, American journal of medical genetics. Part A.

Erratum: Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation( Pediatrics (2008) 121 (404-410))

C. Romano, E. Zackai, H. Hoyme, 2008 .

The effects of fetal alcohol syndrome on response execution and inhibition: an event-related potential study.

C. Nelson, J. Jacobson, C. Andrew, 2009, Alcoholism, clinical and experimental research.

Hyalinosis, Inherited Systemic

H. Hoyme, L. Arbour, Joseph T C Shieh, 2013 .

Systemic Hyalinosis: A Distinctive Early Childhood–Onset Disorder Characterized by Mutations in the Anthrax Toxin Receptor 2 Gene (ANTRX2)

C. Sandborg, H. Hoyme, J. Martignetti, 2006, Pediatrics.

Terminal deletion of 6p results in a recognizable phenotype

H. Hoyme, L. Hudgins, A. Cherry, 2005, American journal of medical genetics. Part A.

The clinical picture of the Börjeson–Forssman–Lehmann syndrome in males and heterozygous females with PHF6 mutations

J. Gécz, B. D. de Vries, J. Clayton-Smith, 2004, Clinical genetics.

Congenital Oral Tumor Associated with Neurofibromatosis Detected by Prenatal Ultrasound

H. Hoyme, S. Musgrave, J. J. Clemmons, 1987, Clinical pediatrics.

Bronchoscopic evaluation of airway obstruction in campomelic dysplasia

H. Hoyme, P. Sammut, J. Britton, 1987, Pediatric pulmonology.

A Decision Tree to Identify Children Affected by Prenatal Alcohol Exposure.

E. Sowell, C. Coles, E. Riley, 2016, The Journal of pediatrics.

Prevalence and characteristics of fetal alcohol syndrome and partial fetal alcohol syndrome in a Rocky Mountain Region City.

H. Hoyme, P. May, J. Gossage, 2015, Drug and alcohol dependence.

Prevalence and Characteristics of Fetal Alcohol Spectrum Disorders

H. Hoyme, P. May, David Buckley, 2014, Pediatrics.

Maternal alcohol consumption producing fetal alcohol spectrum disorders (FASD): quantity, frequency, and timing of drinking.

B. Tabachnick, C. Parry, S. Seedat, 2013, Drug and alcohol dependence.

Clinical delineation of fetal alcohol spectrum disorders (FASD) in Italian children: Comparison and contrast with other racial/ethnic groups and implications for diagnosis and prevention

H. Hoyme, P. May, J. Gossage, 2007, Neuroscience & Biobehavioral Reviews.

Fetal alcohol spectrum disorders in Finland: Clinical delineation of 77 older children and adolescents

Marit Korkman, Ilona Autti-Rämö, I. Autti-Rämö, 2006, American journal of medical genetics. Part A.

Fetal Alcohol Spectrum Disorders in a Southeastern County of the United States: Child Characteristics and Maternal Risk Traits.

B. Tabachnick, H. Hoyme, P. May, 2020, Alcoholism, clinical and experimental research.

Further delineation of the epidermal nevus syndrome: two cases with new findings and literature review.

H. Hoyme, M. Rimsza, T. Grebe, 1993, American journal of medical genetics.

Neuroimaging findings in macrocephaly–capillary malformation: A longitudinal study of 17 patients

E. Zackai, B. Harding, J. Graham, 2007, American journal of medical genetics. Part A.

Blepharophimosis: a causally heterogeneous malformation frequently associated with developmental disabilities.

H. Hoyme, C. Cunniff, S. Hassed, 1998, American journal of medical genetics.

Autosomal dominant microtia and ocular coloboma: New syndrome or an extension of the oculo‐auriculo‐vertebral spectrum?

H. Hoyme, L. Hudgins, A. Beck, 2005, American journal of medical genetics. Part A.

Elements of morphology: Standard terminology for the head and face

H. Hoyme, J. Allanson, M. Muenke, 2009, American journal of medical genetics. Part A.

Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.

H. Hoyme, J. Carey, H. Toriello, 1997, American journal of medical genetics.

Anal atresia and the Klein-Waardenburg syndrome SUMMARY

H. Hoyme, K. Jones, J. O'brien, 2022 .

Prenatal cocaine exposure and fetal vascular disruption.

H. Hoyme, K. Jones, L. Robinson, 1990, Pediatrics.

Carbohydrate metabolism in Acanthamoeba castellanii. I. The activity of key enzymes and (14C)-glucose metabolism.

H. Hoyme, L. M. Prescott, E. Hui, 1973, Canadian journal of microbiology.

The Embryology of Birth Defects

H. Hoyme, K. Jones, 1983 .

Vascular pathogenesis of transverse limb reduction defects.

K. Benirschke, H. Hoyme, K. Jones, 1982, The Journal of pediatrics.

Gastroschisis: abdominal wall disruption secondary to early gestational interruption of the omphalomesenteric artery.

H. Hoyme, K. Jones, M. Jones, 1983, Seminars in perinatology.

The vascular pathogenesis of gastroschisis: intrauterine interruption of the omphalomesenteric artery.

H. Hoyme, K. Jones, K. L. Jones, 1981, The Journal of pediatrics.

Sudden death in Williams syndrome: report of ten cases.

C. Morris, H. Hoyme, L. Bird, 1996, The Journal of pediatrics.

Unilateral aquagenic wrinkling of the palms associated with aspirin intake.

H. Hoyme, A. Bruckner, P. Khuu, 2006, Archives of dermatology.

Neu–Laxova syndrome: Detailed prenatal diagnostic and post‐mortem findings and literature review

H. Hoyme, Y. El‐Sayed, C. Cunniff, 2004, American journal of medical genetics. Part A.

Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection.

H. Hoyme, A. Madan, R. Olney, 2001, American journal of medical genetics.

Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.

S. Schwartz, H. Hoyme, L. Hudgins, 2004, Pediatrics.

Pathogenesis of sirenomelia: an editorial comment.

H. Hoyme, H. Hoyme, 1988, Teratology.

Core Concepts: Chromosome Aneuploidies

H. Hoyme, P. Crotwell, 2012 .

Mutations in PHF6 are associated with Börjeson–Forssman–Lehmann syndrome

M. Shaw, J. Gécz, J. Clayton-Smith, 2002, Nature Genetics.

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

E. Zackai, A. Guttmacher, M. Bamshad, 2005, American journal of human genetics.

Fetal Alcohol Spectrum Disorders: Diagnostic Considerations for Children with a History of Trauma

H. Hoyme, D. Shapiro, Prachi E Shah, 2018 .

RECENT IN-SCHOOL STUDIES

H. Hoyme, P. May, J. Gossage, 2009 .

Fetal alcohol spectrum disorders

S. Popova, E. Riley, H. Hoyme, 2015, Nature Reviews Disease Primers.

Alcohol consumption and other maternal risk factors for fetal alcohol syndrome among three distinct samples of women before, during, and after pregnancy: The risk is relative

Denis L Viljoen, H. Hoyme, P. May, 2004, American journal of medical genetics. Part C, Seminars in medical genetics.

Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome.

A. Guttmacher, H. Hoyme, V. D. Der Kaloustian, 1991, American journal of medical genetics.

Adaptive behaviour in children and adolescents with foetal alcohol spectrum disorders: a comparison with specific learning disability and typical development.

I. Autti-Rämö, Å. Fagerlund, H. Hoyme, 2012, European child & adolescent psychiatry.

Risk factors for behavioural problems in foetal alcohol spectrum disorders

I. Autti-Rämö, Å. Fagerlund, H. Hoyme, 2011, Acta paediatrica.

Fetal Alcohol Spectrum Disorders in a Midwestern City: Child Characteristics, Maternal Risk Traits, and Prevalence.

B. Tabachnick, H. Hoyme, P. May, 2020, Alcoholism, clinical and experimental research.

Updated Clinical Guidelines for Diagnosing Fetal Alcohol Spectrum Disorders

C. Coles, E. Riley, H. Hoyme, 2016, Pediatrics.

Who is most affected by prenatal alcohol exposure: Boys or girls?

B. Tabachnick, C. Parry, S. Seedat, 2017, Drug and alcohol dependence.

Ocular measurements in fetal alcohol spectrum disorders

B. Tabachnick, H. Hoyme, P. May, 2020, American journal of medical genetics. Part A.

Teratology in pediatric practice.

H. Hoyme, L. Seaver, 1992, Pediatric clinics of North America.

Facial Dysmorphism Across the Fetal Alcohol

Peter Hammond, Joseph L. Jacobson, Ernesta M. Meintjes, 2016 .

A South African mixed race lip/philtrum guide for diagnosis of fetal alcohol spectrum disorders

H. Hoyme, P. May, David Buckley, 2015, American journal of medical genetics. Part A.

Fetal alcohol spectrum disorders: Extending the range of structural defects

H. Hoyme, L. Robinson, C. Chambers, 2010, American journal of medical genetics. Part A.

Fetal alcohol spectrum disorders: A practical clinical approach to diagnosis

H. Hoyme, M. Manning, 2007, Neuroscience & Biobehavioral Reviews.

Toluene embryopathy: delineation of the phenotype and comparison with fetal alcohol syndrome.

H. Hoyme, M. Rimsza, L. Seaver, 1994, Pediatrics.

The epidemiology of fetal alcohol syndrome and partial FAS in a South African community.

H. Hoyme, P. May, J. Gossage, 2007, Drug and alcohol dependence.

Fetal alcohol syndrome epidemiology in a South African community: a second study of a very high prevalence area.

H. Hoyme, P. May, P. Kodituwakku, 2005, Journal of studies on alcohol.

Duplication (17p) in a child with an isodicentric (17p) chromosome.

H. Hoyme, J. Mascarello, M. Jones, 1983, American journal of medical genetics.

Autosomal dominant ectrodactyly and absence of long bones of upper or lower limbs: further clinical delineation.

H. Hoyme, K. Jones, R. Pauli, 1987, Jornal de Pediatria.

Vascular pathogenesis of unilateral craniofacial defects.

H. Hoyme, K. Jones, L. Robinson, 1987, The Journal of pediatrics.

Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway.

P. Byers, V. McKusick, H. Hoyme, 2004, American journal of human genetics.

Methotrexate/misoprostol embryopathy: Report of four cases resulting from failed medical abortion

H. Hoyme, G. Enns, A. Beck, 2003, American journal of medical genetics. Part A.

Marked variability in the radiographic features of cartilage‐hair hypoplasia: Case report and review of the literature

H. Hoyme, M. Manning, L. Zollars, 2012, American journal of medical genetics. Part A.

von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.

H. Hoyme, S. Kahler, M. Lubinsky, 1994, American journal of medical genetics.

Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure

E. Sowell, C. Coles, P. Hammond, 2017, Alcoholism, clinical and experimental research.

Replication of High Fetal Alcohol Spectrum Disorders Prevalence Rates, Child Characteristics, and Maternal Risk Factors in a Second Sample of Rural Communities in South Africa

B. Tabachnick, C. Parry, S. Seedat, 2017, International journal of environmental research and public health.

Estimating the community prevalence, child traits, and maternal risk factors of fetal alcohol spectrum disorders (FASD) from a random sample of school children.

H. Hoyme, P. May, David Buckley, 2021, Drug and alcohol dependence.

Evolution of the Physical Phenotype of Fetal Alcohol Spectrum Disorders from Childhood through Adolescence.

J. Jacobson, H. Hoyme, S. Jacobson, 2020, Alcoholism, clinical and experimental research.

Fetal Alcohol Spectrum Disorders in a Rocky Mountain Region City: Child Characteristics, Maternal Risk Traits, and Prevalence.

B. Tabachnick, H. Hoyme, P. May, 2020, Alcoholism, clinical and experimental research.

The continuum of fetal alcohol spectrum disorders in a community in South Africa: Prevalence and characteristics in a fifth sample.

B. Tabachnick, C. Parry, S. Seedat, 2016, Drug and alcohol dependence.

Approaching the prevalence of the full spectrum of fetal alcohol spectrum disorders in a South African population-based study.

C. Parry, S. Seedat, H. Hoyme, 2013, Alcoholism, clinical and experimental research.

The continuum of fetal alcohol spectrum disorders in four rural communities in South Africa: Prevalence and characteristics.

B. Tabachnick, C. Parry, S. Seedat, 2016, Drug and alcohol dependence.

Relationship between dysmorphic features and general cognitive function in children with fetal alcohol spectrum disorders

I. Autti-Rämö, Å. Fagerlund, H. Hoyme, 2007, American journal of medical genetics. Part A.

Developmental disorders of the lymphatic system.

H. Hoyme, M. Witte, C. Witte, 1993, Lymphology.

Trisomy 18 with ectopia cordis, omphalocele, and ventricular septal defect: case report.

H. Hoyme, J. J. Clemmons, L. Roe, 1986, Pediatric pathology.

Maternal Factors Predicting Cognitive and Behavioral Characteristics of Children with Fetal Alcohol Spectrum Disorders

B. Tabachnick, H. Hoyme, P. May, 2013, Journal of developmental and behavioral pediatrics : JDBP.

Maternal risk factors predicting child physical characteristics and dysmorphology in fetal alcohol syndrome and partial fetal alcohol syndrome.

B. Tabachnick, H. Hoyme, P. May, 2011, Drug and alcohol dependence.

Clinical and molecular diagnosis of Miller-Dieker syndrome.

D. Ledbetter, H. Hoyme, W. Dobyns, 1991, American journal of human genetics.

Triplication of 8p22–8p23 in a patient with features similar to Kabuki syndrome

H. Hoyme, L. Hudgins, A. Cherry, 2006, American journal of medical genetics. Part A.

Prenatal alcohol exposure alters the patterns of facial asymmetry.

Ting-kai Li, C. Klingenberg, I. Autti-Rämö, 2010, Alcohol.

Efficacy of Maternal Choline Supplementation During Pregnancy in Mitigating Adverse Effects of Prenatal Alcohol Exposure on Growth and Cognitive Function: A Randomized, Double‐Blind, Placebo‐Controlled Clinical Trial

J. Herbert, M. Stanton, J. Jacobson, 2018, Alcoholism, clinical and experimental research.

Presentation of mucopolysaccharidosis VII (beta-glucuronidase deficiency) in infancy.

H. Hoyme, K. Jones, J. O'brien, 1981, Journal of medical genetics.

Progressive and symmetric supraorbital hyperostosis with bony and soft tissue overgrowth in an Ethiopian female: A newly recognized overgrowth syndrome?

H. Hoyme, M. Adam, K. Cusmano-Ozog, 2008, American journal of medical genetics. Part A.

Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome.

H. Hoyme, L. Seaver, L. Joffe, 1993, American journal of medical genetics.

The role of novel COQ8B mutations in glomerulopathy and related kidney defects

Maureen K. Galindo, H. Hoyme, T. Tomasiak, 2020, American journal of medical genetics. Part A.

The vascular pathogenesis of some sporadically occurring limb defects.

H. Hoyme, K. Jones, M. V. Van Allen, 1983, Seminars in perinatology.

Pharmacogenomics: the future of drug therapy

H. Hoyme, Y J Tsai, H E Hoyme, 2002, Clinical genetics.

Multifaceted case management during pregnancy is associated with better child outcomes and less fetal alcohol syndrome

S. Seedat, H. Hoyme, P. May, 2023, Annals of medicine.

Prevalence of Children with Severe Fetal Alcohol Spectrum Disorders in Communities Near Rome, Italy: New Estimated Rates Are Higher than Previous Estimates

H. Hoyme, P. May, J. Gossage, 2011, International journal of environmental research and public health.

Maternal risk factors for fetal alcohol spectrum disorders in a province in Italy.

B. Tabachnick, H. Hoyme, P. May, 2014, Drug and alcohol dependence.

Characteristic physical traits of first‐grade children in the United States with fetal alcohol spectrum disorders (FASD) and associated alcohol and drug exposures

H. Hoyme, P. May, David Buckley, 2022, American journal of medical genetics. Part A.

The prevalence, child characteristics, and maternal risk factors for the continuum of fetal alcohol spectrum disorders: A sixth population-based study in the same South African community.

B. Tabachnick, C. Parry, S. Seedat, 2020, Drug and alcohol dependence.

Early-Life Predictors of Fetal Alcohol Spectrum Disorders

C. Parry, S. Seedat, H. Hoyme, 2019, Pediatrics.

Computer-Aided Recognition of Facial Attributes for Fetal Alcohol Spectrum Disorders

H. Hoyme, P. May, David Buckley, 2017, Pediatrics.

Breastfeeding and maternal alcohol use: Prevalence and effects on child outcomes and fetal alcohol spectrum disorders.

B. Tabachnick, C. Parry, S. Seedat, 2016, Reproductive toxicology.

Fetal alcohol spectrum disorders and assessment of maxillary and mandibular arc measurements

H. Hoyme, P. May, L. Robinson, 2016, American journal of medical genetics. Part A.

Dietary intake, nutrition, and fetal alcohol spectrum disorders in the Western Cape Province of South Africa.

H. Hoyme, P. May, J. Gossage, 2014, Reproductive toxicology.

An FMRI study of number processing in children with fetal alcohol syndrome.

Christopher J. Cannistraci, J. Gore, J. Gatenby, 2010, Alcoholism, clinical and experimental research.

Population Differences in Dysmorphic Features Among Children With Fetal Alcohol Spectrum Disorders

B. Tabachnick, H. Hoyme, P. May, 2010, Journal of developmental and behavioral pediatrics : JDBP.

Vascular etiology of disruptive structural defects in monozygotic twins.

H. Hoyme, K. Jones, M. Higginbottom, 1981, Pediatrics.

Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome: an additional clinical observation.

A. Guttmacher, H. Hoyme, V. D. Der Kaloustian, 1992, American journal of medical genetics.

Follow-up of children of depressed mothers exposed or not exposed to antidepressant drugs during pregnancy.

H. Hoyme, B. Fleisher, A. Gilles, 2003, The Journal of pediatrics.

Meconium Fatty Acid Ethyl Esters (faees) As Predictors Of Severity Of Fetal Alcohol Spectrum Disorder: 675

J. Jacobson, H. Hoyme, D. Viljoen, 2006 .

Heavy Prenatal Alcohol Exposure is Related to Smaller Corpus Callosum in Newborn MRI Scans

Lilla Zöllei, J. Jacobson, S. Warfield, 2017, Alcoholism, clinical and experimental research.

Modelling of Suspended Sediment Dynamics in Tidal Channels of the German Bight

H. Hoyme, C. Winter, R. Mayerle, 2005 .

Modelling of Medium-Scale Morphodynamics in a Tidal Flat Area in the South-Eastern German Bight

H. Hoyme, R. Mayerle, J. Wilkens, 2005 .

Modelling of Waves in a Tidal Flat Area in the South-Eastern German Bight

H. Hoyme, J. Wilkens, I. Junge, 2005 .

Evaluation of a Formal Pediatric Faculty Mentorship Program.

H. Hoyme, A. Chatterjee, J. Giancola, 2018, South Dakota medicine : the journal of the South Dakota State Medical Association.

Marinesco–Sjögren syndrome in a male with mild dysmorphism

S. Packman, H. Hoyme, M. Golabi, 2005, American journal of medical genetics. Part A.

Design, Construction, and Testing of a Stereo-Photogrammetric Tool for the Diagnosis of Fetal Alcohol Syndrome in Infants

Tania S. Douglas, Ernesta M. Meintjes, Julian Smit, 2009, IEEE Transactions on Medical Imaging.

A brief history of autism, the autism/vaccine hypothesis and a review of the genetic basis of autism spectrum disorders.

H. Hoyme, P. Crotwell, J. Blake, 2013, South Dakota medicine : the journal of the South Dakota State Medical Association.

Interactive feature visualization and detection for 3D face classification

Shiaofen Fang, Tatiana Foroud, Sandra Jacobson, 2010, 9th IEEE International Conference on Cognitive Informatics (ICCI'10).

Relation over time between facial measurements and cognitive outcomes in fetal alcohol-exposed children.

J. Jacobson, H. Hoyme, E. Moore, 2012, Alcoholism, clinical and experimental research.

Bacteremia in the old hemodialysis patient

H. Hoyme, B. Beckers, D. Larbig, 1993 .

Impaired eyeblink conditioning in children with fetal alcohol syndrome.

Christopher D Molteno, M. Stanton, J. Jacobson, 2008, Alcoholism, clinical and experimental research.

Morphogenesis: Re: Clinical, natural history, and imaging information on patients included in reports

R. Stevenson, J. Graham, H. Hoyme, 2003, American journal of medical genetics. Part A.

22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay.

H. Hoyme, M. Manning, K. Cusmano-Ozog, 2007, American journal of medical genetics. Part C, Seminars in medical genetics.

Commentary on the decision of the American Board of Medical Genetics and Genomics to create a 24-month specialty of Laboratory Genetics and Genomics

S. Schwartz, F. Bieber, R. Stevenson, 2016, Genetics in Medicine.

Developmental pathogenesis of short palpebral fissure length in children with fetal alcohol syndrome.

H. Hoyme, L. Robinson, L. Bakhireva, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Neonatal hemorrhage secondary to thrombocytopenia: an occasional effect of prenatal hydantoin exposure.

H. Hoyme, M. Markarian, T. Page, 1982, Birth defects original article series.

Minor malformations. Significant or insignificant?

H. Hoyme, 1987, American journal of diseases of children.

Diagnosis and management of the adolescent boy with Klinefelter syndrome.

H. Hoyme, M. Manning, 2002, Adolescent medicine.

Facial Dysmorphism Across the Fetal Alcohol Spectrum

P. Hammond, M. Suttie, J. Jacobson, 2013, Pediatrics.

Fetal alcohol spectrum disorders

H. Hoyme, M. E. Charness, Edward P. Riley, 2023, Nature Reviews Disease Primers.