| Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21. 3-q22. 1 SW Scherer, P Poorkaj, T Allen, J Kim, D Geshuri, M Nunes, S Soder, ... American journal of human genetics 55 (1), 12, 1994 | 128 | 1994 |
| FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases JA Crolla, F Long, H Rivera, NR Dennis American journal of medical genetics 75 (4), 355-366, 1998 | 112 | 1998 |
| Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere PE Warburton, M Dolled, R Mahmood, A Alonso, S Li, K Naritomi, ... The American Journal of Human Genetics 66 (6), 1794-1806, 2000 | 108 | 2000 |
| Clinical and genetic heterogeneity in patients with mosaic variegated aneuploidy: delineation of clinical subtypes H García‐Castillo, AI Vásquez‐Velásquez, H Rivera, P Barros‐Núñez American journal of medical genetics Part A 146 (13), 1687-1695, 2008 | 103 | 2008 |
| Peutz‐Jeghers syndrome with feminizing Sertoli cell tumor JM Cantú, H Rivera, R Ocampo‐Campos, N Bedolla, V Cortés‐Gallegos, ... Cancer 46 (1), 223-228, 1980 | 102 | 1980 |
| Chromosomal abnormalities in couples with reproductive disorders JP Meza-Espinoza, L Ortiz Anguiano, H Rivera Gynecologic and obstetric investigation 66 (4), 237-240, 2008 | 84 | 2008 |
| A new form of hypertrichosis inherited as an X-linked dominant trait MA Macias-Flores, D Garcia-Cruz, H Rivera, M Escobar-Luján, ... Human genetics 66, 66-70, 1984 | 71 | 1984 |
| Severe Silver-Russell syndrome and translocation (17; 20)(q25; q13) ML Ramirez-Duenas, C Medina, R Ocampo-Campos, H Rivera Clinical genetics 41 (1), 51-53, 1992 | 69 | 1992 |
| Retinoblastoma-del (13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase D H Rivera, C Turleau, J de Grouchy, C Junien, S Despoisse, JM Zucker Human Genetics 59, 211-214, 1981 | 65 | 1981 |
| Nonreciprocal and jumping translocations of 15q1→ qter in Prader‐Willi syndrome H Rivera, O Zuffardi, L Gargantini American journal of medical genetics 37 (3), 311-317, 1990 | 60 | 1990 |
| Fake peer review and inappropriate authorship are real evils H Rivera Journal of Korean Medical Science 34 (2), 2019 | 53 | 2019 |
| Langer-Giedion syndrome with and without del 8q. Assignment of critical segment to 8q23 C Turleau, F Chavin-Colin, J De Grouchy, P Maroteaux, H Rivera Human Genetics 62, 183-187, 1982 | 47 | 1982 |
| Tetrasomy 18p: a distinctive syndrome. H Rivera, M Möller, A Hernandez, MA Enriquez-Guerra, R Arreola, ... Annales de genetique 27 (3), 187-189, 1984 | 45 | 1984 |
| inv (9)(p24q13) in three sterile brothers IP Dávalos, F Rivas, AL Ramos, C Galaviz, L Sandoval, H Rivera Annales de genetique 43 (1), 51-54, 2000 | 43 | 2000 |
| Retractions, fake peer reviews, and paper mills H Rivera, JAT da Silva Journal of Korean Medical Science 36 (24), 2021 | 41 | 2021 |
| Trisomy 22q12 leads to qter:" aneusomie de recombinaison" of a pericentric inversion JM Cantu, A Hernandez, G Vaca, L Plascencia, C Martinez-Basalo, ... Annales de genetique 24 (1), 37-40, 1981 | 39 | 1981 |
| De novo del (6)(q25) associated with macular degeneration. F Rivas, C Ruiz, H Rivera, M Möller, JI Serrano-Lucas, JM Cantu Annales de Genetique 29 (1), 42-44, 1986 | 38 | 1986 |
| Chromosome imbalance, normal phenotype, and imprinting. L Bortotto, E Piovan, R Furlan, H Rivera, O Zuffardi Journal of medical genetics 27 (9), 582-587, 1990 | 37 | 1990 |
| Deletion of 7q22 and ectrodactyly. H Rivera, J Sanchez-Corona, VR Burgos-Fuentes, MJ Melendez-Ruiz Genetic counseling (Geneva, Switzerland) 2 (1), 27-31, 1991 | 35 | 1991 |
| Pure monosomy and trisomy 2q24. 2→ q3105 due to an inv ins (7; 2)(q21. 2; q3105q24. 2) segregating in four generations M Moller, D Garcia-Cruz, H Rivera, J Sanchez-Corona, JM Cantú Human genetics 68, 77-86, 1984 | 34 | 1984 |
