| 1 | Moderate altitude as a risk factor for isolated congenital malformations. Results from a case?control multicenter?multiregional study | Coautor: Mutchinick O.M., Ibarra-Ibarra B.R., Luna-Muñoz L., Arteaga-Vázquez J. | 2024 | Birth Defects Research | WoS-id: 001279809300001
Scopus-id: 2-s2.0-85199617940
| 1 | 1 |
| 2 | Telomeres Length Variations in a Rheumatoid Arthritis Patients Cohort at Early Disease Onset and after Follow-Up | Coautor: Mutchinick O.M., Svyryd Y., Pascual-Ramos V., Contreras-Yañez I., et al. | 2022 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 001260859100004
Scopus-id: 2-s2.0-85138127646
| 3 | 3 |
| 3 | Myelomeningocele genotype?phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways | Coautor: Mutchinick O.M., Ortiz-Cruz G., Aguayo-Gómez A., Luna-Muñoz L., et al. | 2021 | Birth Defects Research | WoS-id: 000608712200001
Scopus-id: 2-s2.0-85100111064
| 7 | 7 |
| 4 | Survival of infants born with esophageal atresia among 24 international birth defects surveillance programs | Coautor: Mutchinick O.M., Bell J.C., Baynam G., Bergman J.E.H., et al. | 2021 | Birth Defects Research | WoS-id: 000630066500001
Scopus-id: 2-s2.0-85102648750
| 14 | 16 |
| 5 | GMPPA defects cause a neuromuscular disorder with a-dystroglycan hyperglycosylation | Coautor: Mutchinick O.M., Franzka P., Henze H., Jung M.J., et al. | 2021 | JOURNAL OF CLINICAL INVESTIGATION | WoS-id: 000663097700001
Scopus-id: 2-s2.0-85105319657
| 20 | 20 |
| 6 | Prevalence and mortality in children with congenital diaphragmatic hernia: a multicountry study | Coautor: Mutchinick O.M., Politis M.D., Bermejo-Sánchez E., Canfield M.A., et al. | 2021 | ANNALS OF EPIDEMIOLOGY | Scopus-id: 2-s2.0-85098163350
| 0 | 71 |
| 7 | Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases | Coautor: Mutchinick O.M., Mensa-Vilaró A., Bravo García-Morato M., de la Calle-Martin O., et al. | 2019 | JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY | WoS-id: 000454918300039
Scopus-id: 2-s2.0-85055716197
| 62 | 62 |
| 8 | OEIS complex: Prevalence, clinical, and epidemiologic findings in a multicenter Mexican birth defects surveillance program | Coautor: Mutchinick O.M., Arteaga-Vázquez J., Luna-Muñoz L., Morales-Suárez J.J. | 2019 | Birth Defects Research | WoS-id: 000473561000006
Scopus-id: 2-s2.0-85065236614
| 10 | 11 |
| 9 | Isolated postaxial polydactyly: Epidemiologic characteristics from a multicenter birth defects study | Coautor: Mutchinick O.M., Ortiz-Cruz G., Luna-Muñoz L., Arteaga-Vázquez J. | 2019 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000478591600008
Scopus-id: 2-s2.0-85065975192
| 4 | 5 |
| 10 | Catalytically Impaired TYK2 Variants are Protective Against Childhood- and Adult-Onset Systemic Lupus Erythematosus in Mexicans | Coautor: Mutchinick O.M., Contreras-Cubas C., García-Ortiz H., Velázquez-Cruz R., et al. | 2019 | SCIENTIFIC REPORTS | WoS-id: 000481999500019
Scopus-id: 2-s2.0-85071008674
| 12 | 15 |
| 11 | PPP2R2B hypermethylation causes acquired apoptosis deficiency in systemic autoimmune diseases | Coautor: Mutchinick O.M., Madera-Salcedo I.K., Sánchez-Hernández B.E., Svyryd Y., et al. | 2019 | Jci Insight | WoS-id: 000482229000006
Scopus-id: 2-s2.0-85071539352
| 21 | 22 |
| 12 | Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980?2010 | Coautor: Mutchinick O.M., Yu X., Nassar N., Mastroiacovo P., et al. | 2019 | EUR UROL | WoS-id: 000487930900029
Scopus-id: 2-s2.0-85068463543
| 84 | 96 |
| 13 | Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012 | Coautor: Mutchinick O.M., Bakker M.K., Kancherla V., Canfield M.A., et al. | 2019 | PAEDIATR PERINAT EP | WoS-id: 000491853500001
Scopus-id: 2-s2.0-85074233326
| 25 | 27 |
| 14 | A Novel GMPPA Mutation in Two Adult Sisters with Achalasia, Alacrima, Short Stature, Dysmorphism, and Intellectual Disability | Coautor: Mutchinick O.M., Benítez E.O., Morales J.J., Muñoz L.A., et al. | 2018 | Molecular Syndromology | WoS-id: 000425496900006
Scopus-id: 2-s2.0-85040722394
| 7 | 6 |
| 15 | Using Genetic and Epigenetic Markers to Improve Differential Diagnosis of Prostate Cancer and Benign Prostatic Hyperplasia by Noninvasive Methods in Mexican Patients | Coautor: Mutchinick O.M., Sánchez B.E., Aguayo A., Martínez B., et al. | 2018 | CLIN GENITOURIN CANC | WoS-id: 000439486400019
Scopus-id: 2-s2.0-85044127410
| 14 | 16 |
| 16 | Genetic Risk Determinants for Cigarette Smoking Dependence in Mexican Mestizo Families | Coautor: Mutchinick O.M., Svyryd Y., Ramírez-Venegas A., Sánchez-Hernández B., et al. | 2016 | NICOTINE TOB RES | WoS-id: 000376350700015
Scopus-id: 2-s2.0-84964981505
| 11 | 10 |
| 17 | Heterogenous distribution of MTHFR gene variants among mestizos and diverse amerindian groups from Mexico | Coautor: Mutchinick, O.M., Contreras-Cubas, C., Sánchez-Hernández, B.E., García-Ortiz, H., et al. | 2016 | PLOS ONE | WoS-id: 000383892100069
Scopus-id: 2-s2.0-84991744704
| 33 | 33 |
| 18 | Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: Variable phenotypic expression in three affected sisters from Mexican ancestry | Coautor: Mutchinick O.M., Arteaga M.E., Hunziker W., Teo A.S.M., et al. | 2015 | Renal Failure | WoS-id: 000346633700029
Scopus-id: 2-s2.0-84919460006
| 17 | 17 |
| 19 | Clinical, imaging, and molecular findings in a sample of Mexican families with pantothenate kinase-associated neurodegeneration | Coautor: Mutchinick O.M., Morales-Briceño H., Chacón-Camacho O.F., Pérez-González E.A., et al. | 2015 | CLINICAL GENETICS | WoS-id: 000350052000008
Scopus-id: 2-s2.0-84922760322
| 14 | 14 |
| 20 | Identification of Copy Number Variations in Isolated Tetralogy of Fallot | Coautor: Mutchinick O.M., Aguayo-Gómez A., Arteaga-Vázquez J., Svyryd Y., et al. | 2015 | PEDIATRIC CARDIOLOGY | WoS-id: 000365310800012
Scopus-id: 2-s2.0-84947865860
| 15 | 16 |
| 21 | Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families | Coautor: Mutchinick O.M., Arteaga-Vázquez J., López-Hernández M.A., Svyryd Y. | 2015 | JOURNAL OF COSMETIC DERMATOLOGY | WoS-id: 000368525400005
Scopus-id: 2-s2.0-84958779392
| 2 | 2 |
| 22 | X chromosome monosomy in primary and overlapping autoimmune diseases | Coautor: Mutchinick O.M., Svyryd Y., Hernández-Molina G., Vargas F., et al. | 2012 | AUTOIMMUNITY REVIEWS | WoS-id: 000302185300002
Scopus-id: 2-s2.0-84857505127
| 25 | 25 |
| 23 | Prevalence of esophageal atresia among 18 international birth defects surveillance programs | Coautor: Mutchinick O.M., Nassar N., Leoncini E., Amar E., et al. | 2012 | BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY | WoS-id: 000311234400005
Scopus-id: 2-s2.0-84869388600
| 115 | 126 |
| 24 | Congenital malformations in the offspring of epileptic mothers with and without anticonvulsant treatment [Malformaciones congénitas en hijos de madres epilépticas con y sin tratamiento con anticonvulsivantes] | Coautor y autor de correspondencia: Mutchinick O.M., Arteaga-Vázquez J., Luna-Muñoz L. | 2012 | SALUD PUBLICA DE MEXICO | WoS-id: 000312240600006
Scopus-id: 2-s2.0-84873736755
| 3 | 6 |
| 25 | Prevalence at birth of cleft lip with or without cleft palate: Data from the International Perinatal Database of Typical Oral Clefts (IPDTOC) | Coautor: Mutchinick O., Mastroiacovo P., Maraschini A., Leoncini E., et al. | 2011 | CLEFT PALATE-CRAN J | WoS-id: 000286576900008
Scopus-id: 2-s2.0-79551560639
| 259 | 310 |
| 26 | Conjoined Twins: A Worldwide Collaborative Epidemiological Study of the International Clearinghouse for Birth Defects Surveillance and Research | 1ᵉʳ autor: Mutchinick O.M., Luna-Muñoz L., Amar E., Bakker M.K., et al. | 2011 | AM J MED GENET C | WoS-id: 000296493300004
Scopus-id: 2-s2.0-80054848452
| 123 | 150 |
| 27 | Amelia: A Multi-Center Descriptive Epidemiologic Study in a Large Dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and Overview of the Literature | Coautor: Mutchinick O.M., Bermejo-Sánchez E., Cuevas L., Amar E., et al. | 2011 | AM J MED GENET C | WoS-id: 000296493300005
Scopus-id: 2-s2.0-80054863766
| 26 | 31 |
| 28 | Phocomelia: A Worldwide Descriptive Epidemiologic Study in a Large Series of Cases From the International Clearinghouse for Birth Defects Surveillance and Research, and Overview of the Literature | Coautor: Mutchinick O.M., Bermejo-Sánchez E., Cuevas L., Amar E., et al. | 2011 | AM J MED GENET C | WoS-id: 000296493300006
Scopus-id: 2-s2.0-80054865262
| 26 | 31 |
| 29 | Bladder Exstrophy: An Epidemiologic Study From the International Clearinghouse for Birth Defects Surveillance and Research, and an Overview of the Literature | Coautor: Mutchinick O.M., Siffel C., Correa A., Amar E., et al. | 2011 | AM J MED GENET C | WoS-id: 000296493300007
Scopus-id: 2-s2.0-80054861885
| 58 | 84 |
| 30 | Cloacal Exstrophy: An Epidemiologic Study From the International Clearinghouse for Birth Defects Surveillance and Research | Coautor: Mutchinick O.M., Feldkamp M.L., Botto L.D., Amar E., et al. | 2011 | AM J MED GENET C | WoS-id: 000296493300008
Scopus-id: 2-s2.0-80054861058
| 50 | 65 |
| 31 | Cyclopia: An Epidemiologic Study in a Large Dataset From the International Clearinghouse of Birth Defects Surveillance and Research | Coautor: Mutchinick O.M., Orioli I.M., Amar E., Bakker M.K., et al. | 2011 | AM J MED GENET C | WoS-id: 000296493300009
Scopus-id: 2-s2.0-80054850987
| 20 | 28 |
| 32 | International Trends of Down Syndrome 1993-2004: Births in Relation to Maternal Age and Terminations of Pregnancies | Coautor: Mutchinick O.M., Cocchi G., Gualdi S., Bower C., et al. | 2010 | BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY | WoS-id: 000279716900004
Scopus-id: 2-s2.0-77953299828
| 104 | 125 |
| 33 | How Valid Are the Rates of Down Syndrome Internationally? Findings from the International Clearinghouse for Birth Defects Surveillance and Research | Coautor: Mutchinick O.M., Leoncini E., Botto L.D., Cocchi G., et al. | 2010 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000280115000038
Scopus-id: 2-s2.0-77954096638
| 35 | 38 |
| 34 | Subtelomeric 6p Monosomy and 12q Trisomy in a Patient With a 46,XX,der(6)t(6;12)(p25.3;q24.31) Karyotype: Phenotypic Overlap With Mutchinick Syndrome | Coautor: Mutchinick O.M., Semerci C.N., Cinbis M., Ullmann R., et al. | 2010 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000280115000045
Scopus-id: 2-s2.0-77954118855
| 3 | 3 |
| 35 | Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) in two Mexican brothers harboring a novel mutation in the ECGF1 gene | Coautor y autor de correspondencia: Mutchinick O.M., Monroy N., Kauffer, LRM | 2008 | EUROPEAN JOURNAL OF MEDICAL GENETICS | WoS-id: 000257199100008
Scopus-id: 2-s2.0-43149088948
| 16 | 23 |
| 36 | Diabets, pregnancy and birth defects [Diabetes, embarazo y defectos al nacimiento] | Coautor y autor de correspondencia: Mutchinick O.M., Arteaga J., Luna L. | 2008 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000257299500005
Scopus-id: 2-s2.0-47849118137
| 7 | 7 |
| 37 | Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance systems: Searching for population variations | Coautor: Mutchinick O., Leoncini E., Baranello G., Orioli I.M., et al. | 2008 | BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY | WoS-id: 000258763500005
Scopus-id: 2-s2.0-50249169215
| 69 | 77 |
| 38 | Preferential associations between oral clefts and other major congenital anomalies | Coautor: Mutchinick O., Rittler M., López-Camelo J.S., Castilla E.E., et al. | 2008 | CLEFT PALATE-CRAN J | WoS-id: 000259242700011
Scopus-id: 2-s2.0-52249112486
| 42 | 51 |
| 39 | The role of the X chromosome in immunity and autoimmunity | Coautor: Mutchinick O.M., Hernández-Molina G., Svyryd Y., Sánchez-Guerrero J. | 2007 | AUTOIMMUNITY REVIEWS | WoS-id: 000245112200005
Scopus-id: 2-s2.0-33847060764
| 26 | 27 |
| 40 | Gastroschisis and associated defects: An international study | Coautor: Mutchinick O., Mastroiacovo P., Lisi A., Castilla E.E., et al. | 2007 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000245450200004
Scopus-id: 2-s2.0-34247215475
| 110 | 132 |
| 41 | Environmental influence on the worldwide prevalence of a 776C?G variant in the transcobalamin gene (TCN2) | Coautor: Mutchinick O.M., Guéant J.-L., Chabi N.W., Guéant-Rodriguez R.-M., et al. | 2007 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000247020800002
Scopus-id: 2-s2.0-34250715385
| 36 | 34 |
| 42 | Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: A comparative study in Mexican, West African, and European populations | Coautor: Mutchinick O.M., Guéant-Rodriguez R.-M., Guéant J.-L., Debard R., et al. | 2006 | AMERICAN JOURNAL OF CLINICAL NUTRITION | WoS-id: 000236073100025
Scopus-id: 2-s2.0-33645652119
| 157 | 171 |
| 43 | A rare case of gonadal agenesis with paramesonephric derivatives in a patient with a normal female karyotype | 1ᵉʳ autor: Mutchinick O.M., Morales J.J., Zenteno J.C., Del Castillo C.F. | 2005 | FERTILITY AND STERILITY | WoS-id: 000226445200029
Scopus-id: 2-s2.0-11844250637
| 7 | 7 |
| 44 | Sex and congenital malformations: An international perspective | Coautor: Mutchinick O.M., Lisi A., Botto L.D., Rittler M., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000227966700008
Scopus-id: 2-s2.0-20144383990
| 38 | 45 |
| 45 | Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63 | Coautor: Mutchinick O.M., Zenteno J.C., Berdón-Zapata V., Kofman-Alfaro S. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000227966700011
Scopus-id: 2-s2.0-15744380371
| 11 | 13 |
| 46 | Erratum: Sex and congenital malformations: An international perspective (American Journal of Medical Genetics (DOI 10.1002/ajmg.a.30514)) | Coautor: Mutchinick O.M., Lisi A., Botto L.D., Rittler M., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | Scopus-id: 2-s2.0-20944447001
| 0 | 1 |
| 47 | Renal defects and limb deficiencies in 197 infants: Is it possible to define the "acrorenal syndrome"? | Coautor: Mutchinick O., Kroes H.Y., Olney R.S., Rosano A., et al. | 2004 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000223478900008
Scopus-id: 2-s2.0-4344660021
| 8 | 10 |
| 48 | Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3 | Coautor: Mutchinick O.M., Cardoso C., Leventer R.J., Ward H.L., et al. | 2003 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: 000181972600012
Scopus-id: 2-s2.0-0037385481
| 174 | 216 |
| 49 | Medicine in a genetic and molecular perspective [La medicina en un contexto genético y molecular] | 1ᵉʳ autor y autor de correspondencia: Mutchinick O.M. | 2003 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000183185900016
Scopus-id: 2-s2.0-0038516764
| 1 | 1 |
| 50 | Geographical and ethnic variation of the 677C>T allele of 5, 10 methylenetetrahydrofolate reductase (MTHFR): Findings from over 7000 newborns from 16 areas world wide | Coautor: Mutchinick O.M., Wilcken B., Bamforth F., Li Z., et al. | 2003 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000184761400012
Scopus-id: 2-s2.0-0041326346
| 380 | 422 |
| 51 | Association of Vitamin D receptor polymorphisms with osteoporosis in Mexican postmenopausal women | Coautor: Mutchinick O.M., Lisker R., López M.A., Jasqui S., et al. | 2003 | HUMAN BIOLOGY | WoS-id: 000185465100008
Scopus-id: 2-s2.0-0141540846
| 29 | 30 |
| 52 | Hyperhomocysteinemia as risk factor in a Mexican population [La hiperhomocisteinemia como factor de riesgo en una población Mexicana] | Coautor: Mutchinick O.M., Morales J.J., Sánchez B., Verdejo J., et al. | 2003 | ARCHIVOS DE CARDIOLOGIA DE MEXICO | Scopus-id: 2-s2.0-0042970457
| 0 | 3 |
| 53 | On the symmetry of limb deficiencies among children with multiple congenital anomalies | Coautor: Mutchinick O., Stoll C., Rosano A., Botto L.D., et al. | 2001 | ANN GENET-PARIS | WoS-id: 000168628600005
Scopus-id: 2-s2.0-0035034113
| 9 | 10 |
| 54 | Invited Comment | 1ᵉʳ autor y autor de correspondencia: Mutchinick O.M. | 2001 | NUTRITION REVIEWS | Scopus-id: 2-s2.0-0034882778
| 0 | 0 |
| 55 | Limb defects associated with major congenital anomalies: Clinical and epidemiological study from the international clearinghouse for birth defects monitoring systems | Coautor: Mutchinick O., Rosano A., Botto L.D., Olney R.S., et al. | 2000 | AM J MED GENET | WoS-id: 000087674100006
Scopus-id: 2-s2.0-0034679903
| 52 | 56 |
| 56 | Congenital malformations in twins: An international study | Coautor: Mutchinick O., Mastroiacovo P., Castilla E.E., Arpino C., et al. | 1999 | AM J MED GENET | WoS-id: 000078964100007
Scopus-id: 2-s2.0-0033548577
| 132 | 163 |
| 57 | Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to the LIS1 and the D178379 loci | 1ᵉʳ autor: Mutchinick O.M., Shaffer L.G., Kashork C.D., Cervantes E.I. | 1999 | AM J MED GENET | WoS-id: 000081010100001
Scopus-id: 2-s2.0-0033001282
| 10 | 11 |
| 58 | High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico: A country with a very high prevalence of neural tube defects | 1ᵉʳ autor: Mutchinick O.M., López M.A., Luna L., Waxman J., et al. | 1999 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000084721800005
Scopus-id: 2-s2.0-0343503018
| 91 | 103 |
| 59 | Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype | 2ᵒ autor: Mutchinick O., Canún S., Shaffer L.G., Fernández C. | 1998 | AM J MED GENET | WoS-id: 000077117700003
Scopus-id: 2-s2.0-0031727153
| 8 | 7 |
| 60 | The spectrum of congenital anomalies of the VATER association: An international study | Coautor: Mutchinick O.M., Botto L.D., Khoury M.J., Mastroiacovo P., et al. | 1997 | AM J MED GENET | WoS-id: A1997XG44200002
Scopus-id: 2-s2.0-0030911255
| 187 | 218 |
| 61 | Mutations of the 5a-reductase Type 2 gene in eight Mexican patients from six different pedigrees with 5a-reductase-2 deficiency | Coautor: Mutchinick O., Canto P., Vilchis F., Chévez B., et al. | 1997 | CLINICAL ENDOCRINOLOGY | WoS-id: A1997WN92300007
Scopus-id: 2-s2.0-0030971433
| 53 | 65 |
| 62 | Accidental radiation injury to the hand: Anatomical and physiological considerations | Coautor: Mutchinick O., Berger M.E., Hurtado R., Dunlap J., et al. | 1997 | HEALTH PHYSICS | WoS-id: A1997WJ33800001
Scopus-id: 2-s2.0-0031028699
| 16 | 17 |
| 63 | Failure of adjusted doses of subcutaneous heparin to prevent thromboembolic phenomena in pregnant patients with mechanical cardiac valve prostheses | Coautor: Mutchinick O., Salazar E., Izaguirre R., Verdejo J. | 1996 | JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY | WoS-id: A1996UM59800021
Scopus-id: 2-s2.0-0029992382
| 155 | 187 |
| 64 | Birth defects. A public health problem in Mexico [Los defectos al nacer. Un problema de salud pública en México.] | 2ᵒ autor: Mutchinick O., Jurado-García E., Urrusti-Sanz J., Vargas-García C. | 1996 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0030093743
| 0 | 4 |
| 65 | Genotypes of alcohol-metabolizing enzymes in Mexicans with alcoholic liver cirrhosis | Coautor: Mutchinick-Baringoltz O., Lisker-Yourkowitzky R., Ramirez-Arroyo E., Perez-Rendon G., et al. | 1995 | Archives Of Medical Research | WoS-id: A1995UM15800013
Scopus-id: 2-s2.0-0029612353
| 5 | 7 |
| 66 | World Alliance of Organizations for the Prevention of Birth Defects | Coautor: Mutchinick, O., Botting, B., Czeizel, A., Katz, M., et al. | 1994 | CONGENIT ANOM | Scopus-id: 2-s2.0-84984357006
| 0 | 0 |
| 67 | Mixed gonadal dysgenesis: Clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients | Coautor: Mutchinick O., Mendez J.P., Ulloa-Aguirre A., Kofman-Alfaro S., et al. | 1993 | AM J MED GENET | WoS-id: A1993KZ61000003
Scopus-id: 2-s2.0-0027216138
| 52 | 61 |
| 68 | Monitoring dominant germ cell mutations using skeletal dysplasias registered in malformation registries: An international feasibility study | Coautor: Mutchinick O., Kallen B., Knudsen L.B., Mastroiacovo P., et al. | 1993 | INTERNATIONAL JOURNAL OF EPIDEMIOLOGY | WoS-id: A1993KP20300015
Scopus-id: 2-s2.0-0027394259
| 27 | 30 |
| 69 | Polymorphisms of chromosomes 1, 9, and 16 in Mexican mestizos [Polimorfismos de los cromosomas 1, 9 y 16 en mestizos mexicanos.] | Coautor: Mutchinick O., Armendares S., Buentello L., Gaona O., et al. | 1993 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1993LE23000005
Scopus-id: 2-s2.0-0027571801
| 1 | 0 |
| 70 | An international collaborative study of the epidemiology of esophageal atresia or stenosis | 2ᵒ autor: Mutchinick O., Robert E., Mastroiacovo P., Knudsen L.B., et al. | 1993 | REPRODUCTIVE TOXICOLOGY | WoS-id: A1993MC73900002
Scopus-id: 2-s2.0-0027653905
| 67 | 79 |
| 71 | Mixed gonadal dysgenesis: Clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients | Coautor: Mutchinick O., Méndez J.P., Ulloa-Aguirre A., Kofman-Alfaro S., et al. | 1993 | OBSTET GYNECOL SURV | Scopus-id: 2-s2.0-84935309623
| 0 | 0 |
| 72 | Absence of limbs and gross body wall defects: An epidemiological study of related rare malformation conditions | Coautor: Mutchinick O., Mastroiacovo P., Kallen B., Knudsen L.B., et al. | 1992 | Teratology | WoS-id: A1992JV80300008
Scopus-id: 2-s2.0-0026440550
| 41 | 42 |
| 73 | The cyclops and the mermaid: An epidemiological study of two types of rare malformation | Coautor: Mutchinick O., Källén B., Castilla E.E., Lancaster P.A.L., et al. | 1992 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1992HA97500009
Scopus-id: 2-s2.0-0026512102
| 75 | 88 |
| 74 | An international case-control study on hypospadias the problem with variability and the beauty of diversity | Coautor: Mutchinick O., källén B., Castilla E.E., Robert E., et al. | 1992 | European Journal Of Epidemiology | WoS-id: A1992HQ88100015
Scopus-id: 2-s2.0-0026505001
| 13 | 18 |
| 75 | Hormone therapy during pregnancy and isolated hypospadias: An international case-control study | Coautor: Mutchinick O.M., Källén B.A.J., Martínez-Frías M.L., Castilla E.E., et al. | 1992 | International Journal of Risk and Safety in Medicine | Scopus-id: 2-s2.0-0026775248
| 0 | 26 |
| 76 | Risk for Down syndrome based on maternal ages grouped in intervals of 2 and 5 years in the Mexican population [Riesgo para síndrome de Down por bienios y quinquenios de edad materna en la población mexicana.] | 1ᵉʳ autor: Mutchinick O., Lisker R., Babinsky V. | 1991 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-0026210125
| 0 | 6 |
| 77 | Molecular differentiation of two different translocations producing two apparent Ph chromosomes in a patient with CML | Coautor: Mutchinick O., Gonsebatt M.-E., Lisker R., Ruz L., et al. | 1991 | CANCER GENET CYTOGEN | WoS-id: A1991GE48700014
Scopus-id: 2-s2.0-0026076212
| 1 | 1 |
| 78 | Oral contraceptives in the etiology of isolated hypospadias | Coautor: Mutchinick O., Källén B., Mastroiacovo P., Lancaster P.A.L., et al. | 1991 | Contraception | WoS-id: A1991GA48100007
Scopus-id: 2-s2.0-0025986733
| 38 | 46 |
| 79 | International collaboration in a cluster investigation [3] | 2ᵒ autor: Mutchinick O., Garza A., Cordero J.F., Burse V.W. | 1991 | AMERICAN JOURNAL OF PUBLIC HEALTH | WoS-id: A1991GD21900031
Scopus-id: 2-s2.0-0026341822
| 0 | 0 |
| 80 | Unusual inheritance of Becker type muscular dystrophy | 2ᵒ autor: Mutchinick O., Lisker R., Ruz L. | 1991 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1991GE98800018
Scopus-id: 2-s2.0-0025822589
| 0 | 0 |
| 81 | Risk factors associated with neural tube defects: exposure during the first trimester of gestation [Factores de riesgo asociados a los defectos de cierre del tubo neural: exposición durante el primer trimester de la gestación.] | 1ᵉʳ autor: Mutchinick O., Orozco E., Lisker R., Babinsky V., et al. | 1990 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0025431104
| 0 | 8 |
| 82 | Genetic polymorphism of the human sex hormone-binding globulin: Evidence of an isoelectric focusing variant with normal androgen-binding affinities | Coautor: Mutchinick O., Larrea F., Oliart R.M., Granados J., et al. | 1990 | Journal Of Steroid Biochemistry | WoS-id: A1990EA13000006
Scopus-id: 2-s2.0-0025184733
| 13 | 11 |
| 83 | Human lymphocyte proliferation kinetics in Hanks' BSS supplemented with autologous plasma and in synthetic medium | 2ᵒ autor y autor de correspondencia: Mutchinick O., Gonsebatt M.E. | 1990 | Mutation Research Letters | WoS-id: A1990CZ23700002
Scopus-id: 2-s2.0-0025261162
| 7 | 5 |
| 84 | Weight, length, head circumference and gestational age in newborns with Down syndrome | 1ᵉʳ autor: Mutchinick O., Lisker R., Babinsky V. | 1989 | Brain Dysfunction | Scopus-id: 2-s2.0-0024911163
| 0 | 0 |
| 85 | The Mexican program of Registration and Epidemiologic Surveillance of External Congenital Malformations [Programa Mexicano de "Registro y Vigilancia Epidemiológica de Malformaciones Congénitas Externas".] | 1ᵉʳ autor: Mutchinick O., Lisker R., Babinski V. | 1988 | SALUD PUBLICA DE MEXICO | Scopus-id: 2-s2.0-0023781933
| 0 | 34 |
| 86 | Partial trisomy 1q in the bone marrow of a patient with polycythemia vera [Trisomía parcial 1q en la médula ósea de un paciente con policitemia vera.] | 2ᵒ autor: Mutchinick O., Lisker R., Casas L., Labardini J. | 1988 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1988N561800005
Scopus-id: 2-s2.0-0023782772
| 1 | 1 |
| 87 | Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations | 1ᵉʳ autor: Mutchinick O., Ramos Z., Sanchez F., Ruz L., et al. | 1988 | AM J MED GENET | WoS-id: A1988L664500023
Scopus-id: 2-s2.0-0023847906
| 9 | 10 |
| 88 | Familial malignant pleural mesothelioma. Report of 3 cases [Mesotelioma pleural maligno familiar. Informe de tres casos.] | Coautor: Mutchinick O., Muñoz L., Guzmán J., Ponce de León S., et al. | 1988 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1988T297100012
Scopus-id: 2-s2.0-0024102908
| 7 | 7 |
| 89 | Heterochromatin C sizes distribution of chromosomes 1, 9, 16 and Y in a sample of the Mexican population: comparison of two quantitative methods of measurement. | 1ᵉʳ autor: Mutchinick O., Sánchez F., Lisker R., Armendares S., et al. | 1987 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1987J499200004
Scopus-id: 2-s2.0-0023321995
| 1 | 0 |
| 90 | Cáncer gástrico familiar. | Coautor: Mutchinick O., Lira Pedrín M.A., Ramírez A., Lisker R., et al. | 1987 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1987L953600010
Scopus-id: 2-s2.0-0023432188
| 0 | 2 |
| 91 | Endocrine evaluation in a patient with MURCS association and ovarian agenesis | Coautor: Mutchinick O., Mendez J.P., Ulloa-Aguirre A., Sánchez F.J., et al. | 1986 | EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY | WoS-id: A1986D473800009
Scopus-id: 2-s2.0-0022448656
| 5 | 8 |
| 92 | Endocrine and biochemical studies in a 46,XY phenotypically male infant with 17-ketosteroid reductase deficiency | Coautor: Mutchinick O., Ulloa-Aguirre A., Bassol S., Poo J., et al. | 1985 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | WoS-id: A1985ADU0900003
Scopus-id: 2-s2.0-0021957785
| 26 | 26 |
| 93 | Fetal mortality in sibships with one or more affected members with oral clefts | 1ᵉʳ autor: Mutchinick O., Lisker R., Babinsky V., Santos M.A., et al. | 1985 | AM J MED GENET | WoS-id: A1985ABZ1100014
Scopus-id: 2-s2.0-0021997057
| 2 | 2 |
| 94 | Sex differentiation. II. Abnormalities of the sex chromosomes and changes in gonadal differentiation [Diferenciación sexual. II. Anomalías de los cromosomas sexuales y alteraciones de la diferenciación gonadal.] | 2ᵒ autor: Mutchinick O., Kofman-Alfaro S., Valdés E., Pérez-Palacios G. | 1984 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1984SM58300011
Scopus-id: 2-s2.0-0021299458
| 0 | 0 |
| 95 | Autosomal recessive heredity in a Mexican family with torsion dystonia [Herencia autosómica recesiva en una familia mexicana con distonia de torsión.] | 2ᵒ autor: Mutchinick O., Lisker R., Reyes M.E., Santos M.A., et al. | 1984 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1984TT13200010
Scopus-id: 2-s2.0-0021467648
| 4 | 6 |
| 96 | Absence of correlation between Y chromosome heterochromatin and several anthropometric measurements in a Mexican population | Coautor: Mutchinick O., Armendares S., Lisker R., Sánchez F., et al. | 1983 | HUMAN GENETICS | Scopus-id: 2-s2.0-0020511985
| 0 | 2 |
| 97 | Type A2 brachydactyly associated to zygodactyly in several members of a Mexican family | 2ᵒ autor: Mutchinick O., Lisker R., Santos M.A. | 1983 | ANN GENET-PARIS | Scopus-id: 2-s2.0-0020546098
| 0 | 1 |
| 98 | Sister-chromatid exchanges and cell kinetics in human and rabbit lymphocytes exposed in vivo and in vitro to 2-bromo-a-ergocryptine | 1ᵉʳ autor: Mutchinick O., Gonsebatt Ma.E., Ruz L., Mauleón P., et al. | 1983 | Mutation Research/genetic Toxicology | WoS-id: A1983QK11300018
Scopus-id: 2-s2.0-0020646749
| 5 | 4 |
| 99 | Distribution of ABO blood groups and other genetic markers in mothers of infants with congenital malformations | 2ᵒ autor: Mutchinick O., Lisker R., Pérez-Briceño R., Gómez H., et al. | 1982 | HUMAN HEREDITY | WoS-id: A1982NV22300004
Scopus-id: 2-s2.0-0019997696
| 6 | 3 |
| 100 | Comparative cytogenetic studies in Macaca arctoides with other species of Macaca and man. | Coautor: Mutchinick O., Miranda R., Ruz L., Estrada A. | 1982 | Acta Anthropogenetica | Scopus-id: 2-s2.0-0020341098
| 0 | 4 |
| 101 | Patient with chronic myelogenous leukemia and late appearing Philadelphia chromosome | Coautor: Mutchinick O., Lisker R., Casas L., López-Ariza B., et al. | 1982 | CANCER GENET CYTOGEN | WoS-id: A1982PE26600009
Scopus-id: 2-s2.0-0020361149
| 23 | 23 |
| 102 | Clinical, radiological and genetic characteristics of various types of short-limb dwarfism in the newborn infant [Características clínicas, radiológicas y genéticas de ciertos tipos de enanismo de miembros cortos en el recién nacido.] | 2ᵒ autor y autor de correspondencia: Mutchinick O., Richardson V. | 1982 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-17144455427
| 0 | 0 |
| 103 | Clinical and endocrine spectrum in patients with the 45,X/46,XY karyotype | Coautor: Mutchinick O., Kofman S., Pérez-Palacios G., Medina M., et al. | 1981 | HUMAN GENETICS | WoS-id: A1981MP17900005
Scopus-id: 2-s2.0-0019486991
| 22 | 20 |
| 104 | Constitutive heterochromatin polymorphisms in patients with malignant diseases | Coautor: Mutchinick O., Aguilar L., Lisker R., Ruz L. | 1981 | CANCER | Scopus-id: 2-s2.0-0019501994
| 0 | 30 |
| 105 | The distribution of ABO blood groups in patients with cholelithiasis (author's transl) [Falta de asociación entre los grupos sanguineos del sistema ABO y la colelitiasis.] | 2ᵒ autor: Mutchinick O., Lisker R., Ramos Z., de las Fuentes G. | 1981 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1981ME80100004
Scopus-id: 2-s2.0-0019592843
| 0 | 0 |
| 106 | Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics | 1ᵉʳ autor: Mutchinick O., Ruz L., Gonsebatt M.E., Mauleón P., et al. | 1981 | HUMAN GENETICS | WoS-id: A1981MW58900011
Scopus-id: 2-s2.0-0019846360
| 7 | 6 |
| 107 | Time of first-generation metaphases. I. The effect of various culture media and of fetal calf serum in human lymphocyte cultures | 1ᵉʳ autor: Mutchinick O., Ruz L., Casas L. | 1980 | MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS | WoS-id: A1980KC84200014
Scopus-id: 2-s2.0-0018973227
| 34 | 22 |
| 108 | Environmental mutagenesis. Registration of congenital abnormalities [Estudios sobre mutagenésis ambiental. Registro de malformaciones congénitas.] | 1ᵉʳ autor: Mutchinick O., Lisker R. | 1980 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0019000781
| 0 | 1 |
| 109 | Chronic myelogenous leukemia. Correlation between clinical, laboratory and cytogenetic data (author's transl) [Leucemia granulocitica crónica. Correlación entre los datos citogenéticos, clínicos y de laboratorio.] | Coautor: Mutchinick O., Lisker R., Pérez-Chávez F., Casas L., et al. | 1980 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1980JY74200006
Scopus-id: 2-s2.0-0019004872
| 1 | 1 |
| 110 | Down's syndrome with XYY sex complement. | 1ᵉʳ autor: Mutchinick O., Matayoshi T. | 1980 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1979JG51900006
Scopus-id: 2-s2.0-0019068622
| 3 | 2 |
| 111 | Late-appearing Philadelphia chromosome in two patients with chronic myelogenous leukemia | Coautor: Mutchinick O., Lisker R., Casas L., Pérez-Chávez F., et al. | 1980 | Blood | WoS-id: A1980KQ18200011
Scopus-id: 2-s2.0-0019157874
| 79 | 65 |
| 112 | Frequency of sister chromatid exchanges in severe protein calorie malnutrition | 1ᵉʳ autor: Mutchinick O., Lisker R., Ruz L., Salamanca F., et al. | 1979 | ANN GENET-PARIS | WoS-id: A1979HW05200002
Scopus-id: 2-s2.0-0018712958
| 19 | 17 |
| 113 | Cytogenetic and endocrine studies in a 45,X female subject with spontaneous sexual development | Coautor: Mutchinick O., Lisker R., Jiménez R., Larrea F., et al. | 1979 | AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY | WoS-id: A1979GF46100006
Scopus-id: 2-s2.0-0018352740
| 11 | 9 |
| 114 | Gerodermia osteodysplastica hereditaria: Report of three affected brothers and literature review | Coautor: Mutchinick O., Lisker R., Hernandez A., Martinez-Lavin M., et al. | 1979 | AM J MED GENET | WoS-id: A1979HB84300009
Scopus-id: 2-s2.0-0018573596
| 23 | 22 |
| 115 | 45,X/47,XYY mosaicism in a patient with Turner's syndrome | Coautor y autor de correspondencia: Mutchinick O., Lisker R., Ruz L. | 1978 | HUMAN GENETICS | WoS-id: A1978EU12600013
Scopus-id: 2-s2.0-0017853728
| 2 | 3 |
| 116 | Interchange of sister chromatids as a method of detection of environmental mutagens and carcinogens. Study of laboratory personnel exposed to radiation materials [Intercambio de cromatides hermanas como método para la detección de mutágen | 1ᵉʳ autor: Mutchinick O., Lisker R., Ruz L. | 1978 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-0018111043
| 0 | 0 |
| 117 | Partial trisomies 13 and 22 due to nondisjunction of a maternal reciprocal translocation, t(13;22)(q22;q11) | 1ᵉʳ autor: Mutchinick O., Ruz L., Jiménez R. | 1978 | HUMAN GENETICS | WoS-id: A1978FY97800013
Scopus-id: 2-s2.0-0018135210
| 13 | 8 |
| 118 | Specific patterns of association in homologous acrocentric chromosomes [FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS] | 1ᵉʳ autor y autor de correspondencia: Mutchinick O.M. | 1976 | Excerpta Med., Amsterdam, I.C.S. | Scopus-id: 2-s2.0-0017035582
| 0 | 0 |
| 119 | Centromeric linkage | Coautor: Mutchinick O., Ferguson-Smith M.A., Ellis P.M., Glen K.P., et al. | 1975 | Birth Defects: Original Article Series | WoS-id: A1975AP45700026
Scopus-id: 2-s2.0-0016834709
| 4 | 9 |
| 120 | Centromeric linkage. | Coautor: Mutchinick O., Ferguson-Smith M.A., Ellis P.M., Glen K.P., et al. | 1975 | CYTOGENETICS AND CELL GENETICS | WoS-id: A1975AP45700026
Scopus-id: 2-s2.0-0016637012
| 4 | 4 |
| 121 | Latin American study on congenital malformations [Estudio latinoamericano sobre malformaciones congénitas] | 2ᵒ autor: Mutchinick O., Castilla E., Paz J., Muñoz E., et al. | 1974 | Boletín De La Oficina Sanitaria Panamericana | WoS-id: A1974T466800003
Scopus-id: 2-s2.0-0016074361
| 26 | 21 |
| 122 | Another human chimaera | Coautor: Mutchinick O.M., Battey D.A., Bird G.W.G., McDermott A., et al. | 1974 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1974U364700013
Scopus-id: 2-s2.0-0016349617
| 9 | 9 |
| 123 | Polydactyly: a genetic study in South America | Coautor: Mutchinick O., Castilla E., Paz J., Muñoz E., et al. | 1973 | AMERICAN JOURNAL OF HUMAN GENETICS | WoS-id: A1973Q015800007
Scopus-id: 2-s2.0-0015793262
| 94 | 94 |
| 124 | A syndrome of mental and physical etardation, speech disorders, and peculiar facies in two sisters. | 1ᵉʳ autor y autor de correspondencia: Mutchinick O. | 1972 | JOURNAL OF MEDICAL GENETICS | WoS-id: A1972M081700013
Scopus-id: 2-s2.0-0015311636
| 8 | 10 |
| 125 | A case of Edwards' syndrome with normal karyotype [Un caso de síndrome de Edwards con cariotipo normal.] | Coautor: Mutchinick O., Salgado L., Paz J., Castilla E. | 1970 | Archivos Argentinos de Pediatria | Scopus-id: 2-s2.0-0014904186
| 0 | 0 |
| 126 | A case of Patau's syndrome with trisomy 13. Comments on its occurrence [Acerca de un caso con síndrome de Patau y trisomía 13. Comentarios respecto de su recuencia.] | Coautor: Mutchinick O., Castilla E., Paz J., Fasolino J.N., et al. | 1970 | Archivos Argentinos de Pediatria | Scopus-id: 2-s2.0-0014914521
| 0 | 0 |
ID's SCOPUS 